CN115209735A - 杀真菌组合物 - Google Patents
杀真菌组合物 Download PDFInfo
- Publication number
- CN115209735A CN115209735A CN202180018462.4A CN202180018462A CN115209735A CN 115209735 A CN115209735 A CN 115209735A CN 202180018462 A CN202180018462 A CN 202180018462A CN 115209735 A CN115209735 A CN 115209735A
- Authority
- CN
- China
- Prior art keywords
- methyl
- phenyl
- trifluoromethyl
- oxadiazol
- methoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 179
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 66
- 241000233866 Fungi Species 0.000 claims abstract description 33
- 230000003032 phytopathogenic effect Effects 0.000 claims abstract description 20
- 150000001875 compounds Chemical class 0.000 claims description 243
- -1 5-methyl-2-pyridinyl Chemical group 0.000 claims description 115
- 238000000034 method Methods 0.000 claims description 58
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 52
- 239000004480 active ingredient Substances 0.000 claims description 51
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 49
- 201000010099 disease Diseases 0.000 claims description 46
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 46
- 150000003839 salts Chemical class 0.000 claims description 39
- 239000005730 Azoxystrobin Substances 0.000 claims description 38
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 claims description 38
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 36
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 claims description 35
- 239000005757 Cyproconazole Substances 0.000 claims description 35
- 239000005760 Difenoconazole Substances 0.000 claims description 35
- 239000005857 Trifloxystrobin Substances 0.000 claims description 35
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 claims description 35
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 claims description 35
- MNHVNIJQQRJYDH-UHFFFAOYSA-N 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound N1=CNC(=S)N1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl MNHVNIJQQRJYDH-UHFFFAOYSA-N 0.000 claims description 34
- 239000005825 Prothioconazole Substances 0.000 claims description 34
- 239000005869 Pyraclostrobin Substances 0.000 claims description 31
- VMNULHCTRPXWFJ-UJSVPXBISA-N enoxastrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)\C=C\C1=CC=C(Cl)C=C1 VMNULHCTRPXWFJ-UJSVPXBISA-N 0.000 claims description 31
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 claims description 31
- SXSGXWCSHSVPGB-UHFFFAOYSA-N fluxapyroxad Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC(F)=C(F)C(F)=C1 SXSGXWCSHSVPGB-UHFFFAOYSA-N 0.000 claims description 27
- 239000005788 Fluxapyroxad Substances 0.000 claims description 26
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 claims description 25
- 239000005822 Propiconazole Substances 0.000 claims description 25
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims description 25
- 239000005737 Benzovindiflupyr Substances 0.000 claims description 23
- 239000005747 Chlorothalonil Substances 0.000 claims description 23
- 239000005802 Mancozeb Substances 0.000 claims description 23
- CCCGEKHKTPTUHJ-UHFFFAOYSA-N N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC2=C1C1CCC2C1=C(Cl)Cl CCCGEKHKTPTUHJ-UHFFFAOYSA-N 0.000 claims description 23
- 239000005818 Picoxystrobin Substances 0.000 claims description 23
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims description 23
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 claims description 23
- 235000015097 nutrients Nutrition 0.000 claims description 20
- 238000009472 formulation Methods 0.000 claims description 19
- OCIRCFJCEQNJDN-ATVHPVEESA-N methyl (Z)-2-(5-cyclohexyl-2-methylphenoxy)-3-methoxyprop-2-enoate Chemical compound C1(CCCCC1)C=1C=CC(=C(O\C(\C(=O)OC)=C/OC)C=1)C OCIRCFJCEQNJDN-ATVHPVEESA-N 0.000 claims description 19
- FXEBFDNKQMGJKB-WJDWOHSUSA-N C1(CCCC1)C=1C=CC(=C(O\C(\C(=O)OC)=C/OC)C=1)C Chemical compound C1(CCCC1)C=1C=CC(=C(O\C(\C(=O)OC)=C/OC)C=1)C FXEBFDNKQMGJKB-WJDWOHSUSA-N 0.000 claims description 17
- 239000000463 material Substances 0.000 claims description 17
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 claims description 14
- 239000005787 Flutriafol Substances 0.000 claims description 14
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 14
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 claims description 13
- 239000005767 Epoxiconazole Substances 0.000 claims description 13
- UFEODZBUAFNAEU-NLRVBDNBSA-N fluoxastrobin Chemical compound C=1C=CC=C(OC=2C(=C(OC=3C(=CC=CC=3)Cl)N=CN=2)F)C=1C(=N/OC)\C1=NOCCO1 UFEODZBUAFNAEU-NLRVBDNBSA-N 0.000 claims description 13
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 13
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims description 12
- NGPCLTYABBZNEC-UHFFFAOYSA-N 2-[6-(4-chlorophenoxy)-2-(trifluoromethyl)pyridin-3-yl]-1-(1,2,4-triazol-1-yl)propan-2-ol Chemical compound ClC1=CC=C(OC2=CC=C(C(=N2)C(F)(F)F)C(CN2N=CN=C2)(C)O)C=C1 NGPCLTYABBZNEC-UHFFFAOYSA-N 0.000 claims description 12
- FARWYQWMMZDJPY-UHFFFAOYSA-N 3-[2-(1-chlorocyclopropyl)-3-(3-chloro-2-fluorophenyl)-2-hydroxypropyl]imidazole-4-carbonitrile Chemical compound ClC=1C(=C(C=CC=1)CC(CN1C=NC=C1C#N)(O)C1(CC1)Cl)F FARWYQWMMZDJPY-UHFFFAOYSA-N 0.000 claims description 12
- 239000005796 Ipconazole Substances 0.000 claims description 12
- 239000005868 Metconazole Substances 0.000 claims description 12
- 239000005839 Tebuconazole Substances 0.000 claims description 12
- QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 claims description 12
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 claims description 12
- QCBWUXVEKBGXGM-UHFFFAOYSA-N 2-[6-(4-bromophenoxy)-2-(trifluoromethyl)pyridin-3-yl]-1-(1,2,4-triazol-1-yl)propan-2-ol Chemical compound BrC1=CC=C(OC2=CC=C(C(=N2)C(F)(F)F)C(CN2N=CN=C2)(C)O)C=C1 QCBWUXVEKBGXGM-UHFFFAOYSA-N 0.000 claims description 11
- 239000005738 Bixafen Substances 0.000 claims description 11
- 239000005762 Dimoxystrobin Substances 0.000 claims description 11
- 239000005784 Fluoxastrobin Substances 0.000 claims description 11
- LDLMOOXUCMHBMZ-UHFFFAOYSA-N bixafen Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=C(F)C=C1C1=CC=C(Cl)C(Cl)=C1 LDLMOOXUCMHBMZ-UHFFFAOYSA-N 0.000 claims description 11
- CWVRPJSBNHNJSI-XQNSMLJCSA-N coumoxystrobin Chemical compound C1=C2OC(=O)C(CCCC)=C(C)C2=CC=C1OCC1=CC=CC=C1\C(=C/OC)C(=O)OC CWVRPJSBNHNJSI-XQNSMLJCSA-N 0.000 claims description 11
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 claims description 11
- 239000000575 pesticide Substances 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- HIIRDDUVRXCDBN-OBGWFSINSA-N metominostrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1OC1=CC=CC=C1 HIIRDDUVRXCDBN-OBGWFSINSA-N 0.000 claims description 10
- 239000005562 Glyphosate Substances 0.000 claims description 9
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 9
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 8
- BDHDGBJUDDNROY-ZROIWOOFSA-N C1(CC1)C=1C=CC(=C(O\C(\C(=O)OC)=C/OC)C=1)C Chemical compound C1(CC1)C=1C=CC(=C(O\C(\C(=O)OC)=C/OC)C=1)C BDHDGBJUDDNROY-ZROIWOOFSA-N 0.000 claims description 8
- BLVJYEXSQTXLRS-GDNBJRDFSA-N C1(CCC1)C=1C=CC(=C(O\C(\C(=O)OC)=C/OC)C=1)C Chemical compound C1(CCC1)C=1C=CC(=C(O\C(\C(=O)OC)=C/OC)C=1)C BLVJYEXSQTXLRS-GDNBJRDFSA-N 0.000 claims description 8
- 239000005561 Glufosinate Substances 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 229940097068 glyphosate Drugs 0.000 claims description 8
- 239000011734 sodium Substances 0.000 claims description 8
- IEKSGOPPBDNFFP-UHFFFAOYSA-N N-(2-fluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide Chemical compound FC1=C(C=CC=C1)NC(C1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F)=O IEKSGOPPBDNFFP-UHFFFAOYSA-N 0.000 claims description 7
- 239000002671 adjuvant Substances 0.000 claims description 7
- 239000000417 fungicide Substances 0.000 claims description 7
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims description 7
- 125000004274 oxetan-2-yl group Chemical group [H]C1([H])OC([H])(*)C1([H])[H] 0.000 claims description 7
- 241000894006 Bacteria Species 0.000 claims description 6
- 230000000895 acaricidal effect Effects 0.000 claims description 6
- 239000000642 acaricide Substances 0.000 claims description 6
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 claims description 6
- 239000004308 thiabendazole Substances 0.000 claims description 6
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims description 6
- 235000010296 thiabendazole Nutrition 0.000 claims description 6
- 229960004546 thiabendazole Drugs 0.000 claims description 6
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 claims description 5
- PFFIDZXUXFLSSR-UHFFFAOYSA-N 1-methyl-N-[2-(4-methylpentan-2-yl)-3-thienyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound S1C=CC(NC(=O)C=2C(=NN(C)C=2)C(F)(F)F)=C1C(C)CC(C)C PFFIDZXUXFLSSR-UHFFFAOYSA-N 0.000 claims description 5
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 claims description 5
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 claims description 5
- 108700003918 Bacillus Thuringiensis insecticidal crystal Proteins 0.000 claims description 5
- 241000193388 Bacillus thuringiensis Species 0.000 claims description 5
- KCVSOIVUVIUBHU-UHFFFAOYSA-N BrC=1C=C(C(=NC=1OC(COCCC)C)C)N=CN(C)C(C)C Chemical compound BrC=1C=C(C(=NC=1OC(COCCC)C)C)N=CN(C)C(C)C KCVSOIVUVIUBHU-UHFFFAOYSA-N 0.000 claims description 5
- 239000005816 Penthiopyrad Substances 0.000 claims description 5
- 239000005821 Propamocarb Substances 0.000 claims description 5
- 239000005941 Thiamethoxam Substances 0.000 claims description 5
- 229940097012 bacillus thuringiensis Drugs 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 claims description 5
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 claims description 5
- YABFPHSQTSFWQB-UHFFFAOYSA-N 2-(4-fluorophenyl)-1-(1,2,4-triazol-1-yl)-3-(trimethylsilyl)propan-2-ol Chemical compound C=1C=C(F)C=CC=1C(O)(C[Si](C)(C)C)CN1C=NC=N1 YABFPHSQTSFWQB-UHFFFAOYSA-N 0.000 claims description 4
- XTDZGXBTXBEZDN-UHFFFAOYSA-N 3-(difluoromethyl)-N-(9-isopropyl-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl)-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F XTDZGXBTXBEZDN-UHFFFAOYSA-N 0.000 claims description 4
- 239000005660 Abamectin Substances 0.000 claims description 4
- 239000005740 Boscalid Substances 0.000 claims description 4
- WGPFYKUCVMDGBI-UHFFFAOYSA-N CCN(C)C=NC(C(C)=N1)=CC(Br)=C1OC(C)C Chemical compound CCN(C)C=NC(C(C)=N1)=CC(Br)=C1OC(C)C WGPFYKUCVMDGBI-UHFFFAOYSA-N 0.000 claims description 4
- 239000005886 Chlorantraniliprole Substances 0.000 claims description 4
- 239000005504 Dicamba Substances 0.000 claims description 4
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 claims description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 239000005799 Isopyrazam Substances 0.000 claims description 4
- METKIMKYRPQLGS-UHFFFAOYSA-N atenolol Chemical compound CC(C)NCC(O)COC1=CC=C(CC(N)=O)C=C1 METKIMKYRPQLGS-UHFFFAOYSA-N 0.000 claims description 4
- 229940118790 boscalid Drugs 0.000 claims description 4
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 claims description 4
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 claims description 4
- PSOVNZZNOMJUBI-UHFFFAOYSA-N chlorantraniliprole Chemical compound CNC(=O)C1=CC(Cl)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl PSOVNZZNOMJUBI-UHFFFAOYSA-N 0.000 claims description 4
- 125000000068 chlorophenyl group Chemical group 0.000 claims description 4
- 229960003887 dichlorophen Drugs 0.000 claims description 4
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 4
- OUMSNRPZKWUWES-UHFFFAOYSA-N n-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide Chemical compound C1=CC(C(=O)NC)=CC=C1C1=NOC(C(F)(F)F)=N1 OUMSNRPZKWUWES-UHFFFAOYSA-N 0.000 claims description 4
- NMVCBWZLCXANER-UHFFFAOYSA-N pyriofenone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(Cl)=CN=C1OC NMVCBWZLCXANER-UHFFFAOYSA-N 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- GOLXNESZZPUPJE-UHFFFAOYSA-N spiromesifen Chemical compound CC1=CC(C)=CC(C)=C1C(C(O1)=O)=C(OC(=O)CC(C)(C)C)C11CCCC1 GOLXNESZZPUPJE-UHFFFAOYSA-N 0.000 claims description 4
- XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 claims description 4
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 claims description 4
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 claims description 3
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 claims description 3
- XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 claims description 3
- LKYNGTHMKCTTQC-UHFFFAOYSA-N 1,2-oxazole-3-carboxamide Chemical compound NC(=O)C=1C=CON=1 LKYNGTHMKCTTQC-UHFFFAOYSA-N 0.000 claims description 3
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 claims description 3
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 claims description 3
- ZVXKYWHJBYIYNI-UHFFFAOYSA-N 1h-pyrazole-4-carboxamide Chemical compound NC(=O)C=1C=NNC=1 ZVXKYWHJBYIYNI-UHFFFAOYSA-N 0.000 claims description 3
- VSZBYPXHHDNXJJ-UHFFFAOYSA-N 2-(2-methylpropoxy)quinoline Chemical compound C1=CC=CC2=NC(OCC(C)C)=CC=C21 VSZBYPXHHDNXJJ-UHFFFAOYSA-N 0.000 claims description 3
- HZJKXKUJVSEEFU-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile Chemical compound C=1C=C(Cl)C=CC=1C(CCCC)(C#N)CN1C=NC=N1 HZJKXKUJVSEEFU-UHFFFAOYSA-N 0.000 claims description 3
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 claims description 3
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 claims description 3
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 claims description 3
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 claims description 3
- GOFJDXZZHFNFLV-UHFFFAOYSA-N 5-fluoro-1,3-dimethyl-N-[2-(4-methylpentan-2-yl)phenyl]pyrazole-4-carboxamide Chemical compound CC(C)CC(C)C1=CC=CC=C1NC(=O)C1=C(F)N(C)N=C1C GOFJDXZZHFNFLV-UHFFFAOYSA-N 0.000 claims description 3
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 3
- 239000005894 Emamectin Substances 0.000 claims description 3
- 239000005656 Fenazaquin Substances 0.000 claims description 3
- 239000005775 Fenbuconazole Substances 0.000 claims description 3
- 239000005657 Fenpyroximate Substances 0.000 claims description 3
- 239000005780 Fluazinam Substances 0.000 claims description 3
- 239000005783 Fluopyram Substances 0.000 claims description 3
- 239000005785 Fluquinconazole Substances 0.000 claims description 3
- 239000005661 Hexythiazox Substances 0.000 claims description 3
- 239000005794 Hymexazol Substances 0.000 claims description 3
- XMLSXPIVAXONDL-PLNGDYQASA-N Jasmone Chemical compound CC\C=C/CC1=C(C)CCC1=O XMLSXPIVAXONDL-PLNGDYQASA-N 0.000 claims description 3
- 239000005804 Mandipropamid Substances 0.000 claims description 3
- 239000002169 Metam Substances 0.000 claims description 3
- 239000005809 Metiram Substances 0.000 claims description 3
- 239000005811 Myclobutanil Substances 0.000 claims description 3
- KYGZCKSPAKDVKC-UHFFFAOYSA-N Oxolinic acid Chemical compound C1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC2=C1OCO2 KYGZCKSPAKDVKC-UHFFFAOYSA-N 0.000 claims description 3
- 239000005813 Penconazole Substances 0.000 claims description 3
- 239000005815 Penflufen Substances 0.000 claims description 3
- 239000005819 Potassium phosphonate Substances 0.000 claims description 3
- 239000005663 Pyridaben Substances 0.000 claims description 3
- 239000005658 Tebufenpyrad Substances 0.000 claims description 3
- 239000005840 Tetraconazole Substances 0.000 claims description 3
- 239000005846 Triadimenol Substances 0.000 claims description 3
- 239000005859 Triticonazole Substances 0.000 claims description 3
- 239000005863 Zoxamide Substances 0.000 claims description 3
- 229950008167 abamectin Drugs 0.000 claims description 3
- 150000001413 amino acids Chemical class 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- 230000000844 anti-bacterial effect Effects 0.000 claims description 3
- AKNQMEBLVAMSNZ-UHFFFAOYSA-N azaconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCCO1 AKNQMEBLVAMSNZ-UHFFFAOYSA-N 0.000 claims description 3
- 229950000294 azaconazole Drugs 0.000 claims description 3
- 239000003899 bactericide agent Substances 0.000 claims description 3
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 claims description 3
- OMAAXMJMHFXYFY-UHFFFAOYSA-L calcium trioxidophosphanium Chemical compound [Ca+2].[O-]P([O-])=O OMAAXMJMHFXYFY-UHFFFAOYSA-L 0.000 claims description 3
- IVLCENBZDYVJPA-ARJAWSKDSA-N cis-Jasmone Natural products C\C=C/CC1=C(C)CCC1=O IVLCENBZDYVJPA-ARJAWSKDSA-N 0.000 claims description 3
- 229930003836 cresol Natural products 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- WOWBFOBYOAGEEA-UHFFFAOYSA-N diafenthiuron Chemical compound CC(C)C1=C(NC(=S)NC(C)(C)C)C(C(C)C)=CC(OC=2C=CC=CC=2)=C1 WOWBFOBYOAGEEA-UHFFFAOYSA-N 0.000 claims description 3
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 3
- UOAMTSKGCBMZTC-UHFFFAOYSA-N dicofol Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)(Cl)Cl)(O)C1=CC=C(Cl)C=C1 UOAMTSKGCBMZTC-UHFFFAOYSA-N 0.000 claims description 3
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 claims description 3
- YXXXKCDYKKSZHL-UHFFFAOYSA-M dipotassium;dioxido(oxo)phosphanium Chemical compound [K+].[K+].[O-][P+]([O-])=O YXXXKCDYKKSZHL-UHFFFAOYSA-M 0.000 claims description 3
- GCKZANITAMOIAR-XWVCPFKXSA-N dsstox_cid_14566 Chemical compound [O-]C(=O)C1=CC=CC=C1.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H]([NH2+]C)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 GCKZANITAMOIAR-XWVCPFKXSA-N 0.000 claims description 3
- DMYHGDXADUDKCQ-UHFFFAOYSA-N fenazaquin Chemical compound C1=CC(C(C)(C)C)=CC=C1CCOC1=NC=NC2=CC=CC=C12 DMYHGDXADUDKCQ-UHFFFAOYSA-N 0.000 claims description 3
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 claims description 3
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 claims description 3
- KVDJTXBXMWJJEF-UHFFFAOYSA-N fluopyram Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CCNC(=O)C1=CC=CC=C1C(F)(F)F KVDJTXBXMWJJEF-UHFFFAOYSA-N 0.000 claims description 3
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 claims description 3
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000004312 hexamethylene tetramine Substances 0.000 claims description 3
- KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 0.000 claims description 3
- AGKSTYPVMZODRV-UHFFFAOYSA-N imibenconazole Chemical compound C1=CC(Cl)=CC=C1CSC(CN1N=CN=C1)=NC1=CC=C(Cl)C=C1Cl AGKSTYPVMZODRV-UHFFFAOYSA-N 0.000 claims description 3
- ZQEIXNIJLIKNTD-GFCCVEGCSA-N metalaxyl-M Chemical compound COCC(=O)N([C@H](C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-GFCCVEGCSA-N 0.000 claims description 3
- CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 claims description 3
- 229920000257 metiram Polymers 0.000 claims description 3
- 229960000321 oxolinic acid Drugs 0.000 claims description 3
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 claims description 3
- ZYHMJXZULPZUED-UHFFFAOYSA-N propargite Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(OS(=O)OCC#C)CCCC1 ZYHMJXZULPZUED-UHFFFAOYSA-N 0.000 claims description 3
- KKEJMLAPZVXPOF-UHFFFAOYSA-N pyraziflumid Chemical compound C1=C(F)C(F)=CC=C1C1=CC=CC=C1NC(=O)C1=NC=CN=C1C(F)(F)F KKEJMLAPZVXPOF-UHFFFAOYSA-N 0.000 claims description 3
- DWFZBUWUXWZWKD-UHFFFAOYSA-N pyridaben Chemical compound C1=CC(C(C)(C)C)=CC=C1CSC1=C(Cl)C(=O)N(C(C)(C)C)N=C1 DWFZBUWUXWZWKD-UHFFFAOYSA-N 0.000 claims description 3
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 claims description 3
- 150000003254 radicals Chemical class 0.000 claims description 3
- 229960005322 streptomycin Drugs 0.000 claims description 3
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 claims description 3
- XMLSXPIVAXONDL-UHFFFAOYSA-N trans-jasmone Natural products CCC=CCC1=C(C)CCC1=O XMLSXPIVAXONDL-UHFFFAOYSA-N 0.000 claims description 3
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 claims description 3
- SODPIMGUZLOIPE-UHFFFAOYSA-N (4-chlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(Cl)C=C1 SODPIMGUZLOIPE-UHFFFAOYSA-N 0.000 claims description 2
- ZFHGXWPMULPQSE-SZGBIDFHSA-N (Z)-(1S)-cis-tefluthrin Chemical compound FC1=C(F)C(C)=C(F)C(F)=C1COC(=O)[C@@H]1C(C)(C)[C@@H]1\C=C(/Cl)C(F)(F)F ZFHGXWPMULPQSE-SZGBIDFHSA-N 0.000 claims description 2
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 claims description 2
- OVXMBIVWNJDDSM-UHFFFAOYSA-N (benzhydrylideneamino) 2,6-bis[(4,6-dimethoxypyrimidin-2-yl)oxy]benzoate Chemical compound COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C(=O)ON=C(C=2C=CC=CC=2)C=2C=CC=CC=2)=N1 OVXMBIVWNJDDSM-UHFFFAOYSA-N 0.000 claims description 2
- TUBQDCKAWGHZPF-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethyl thiocyanate Chemical compound C1=CC=C2SC(SCSC#N)=NC2=C1 TUBQDCKAWGHZPF-UHFFFAOYSA-N 0.000 claims description 2
- HHNMEHXDTFYTSO-UHFFFAOYSA-N 1,3-dimethoxy-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea Chemical compound CON(C(=O)NOC)CC1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F HHNMEHXDTFYTSO-UHFFFAOYSA-N 0.000 claims description 2
- OWEGWHBOCFMBLP-UHFFFAOYSA-N 1-(4-chlorophenoxy)-1-(1H-imidazol-1-yl)-3,3-dimethylbutan-2-one Chemical compound C1=CN=CN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 OWEGWHBOCFMBLP-UHFFFAOYSA-N 0.000 claims description 2
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 claims description 2
- KRDJWAGXHSLJIL-UHFFFAOYSA-N 1-methoxy-3-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea Chemical compound CON(C(=O)NC)CC1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F KRDJWAGXHSLJIL-UHFFFAOYSA-N 0.000 claims description 2
- NWVGXXPWOYZODV-UHFFFAOYSA-N 1h-imidazole-5-carbonitrile Chemical compound N#CC1=CN=CN1 NWVGXXPWOYZODV-UHFFFAOYSA-N 0.000 claims description 2
- 239000002794 2,4-DB Substances 0.000 claims description 2
- NCKMMSIFQUPKCK-UHFFFAOYSA-N 2-benzyl-4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1CC1=CC=CC=C1 NCKMMSIFQUPKCK-UHFFFAOYSA-N 0.000 claims description 2
- UCHLUWWJWGEGMO-UHFFFAOYSA-N 3-ethyl-1-methoxy-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea Chemical compound C(C)NC(N(CC1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F)OC)=O UCHLUWWJWGEGMO-UHFFFAOYSA-N 0.000 claims description 2
- NRTLIYOWLVMQBO-UHFFFAOYSA-N 5-chloro-1,3-dimethyl-N-(1,1,3-trimethyl-1,3-dihydro-2-benzofuran-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)OC(C)(C)C2=CC=CC=1NC(=O)C=1C(C)=NN(C)C=1Cl NRTLIYOWLVMQBO-UHFFFAOYSA-N 0.000 claims description 2
- CGRCPZUQMBYVPZ-UHFFFAOYSA-N 5-fluoro-2-[(4-methylphenyl)methoxy]pyrimidin-4-amine Chemical compound C1=CC(C)=CC=C1COC1=NC=C(F)C(N)=N1 CGRCPZUQMBYVPZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000005726 Ametoctradin Substances 0.000 claims description 2
- 239000005727 Amisulbrom Substances 0.000 claims description 2
- 239000005741 Bromuconazole Substances 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 239000005496 Chlorsulfuron Substances 0.000 claims description 2
- 239000005889 Cyantraniliprole Substances 0.000 claims description 2
- 239000005754 Cyazofamid Substances 0.000 claims description 2
- 239000004258 Ethoxyquin Substances 0.000 claims description 2
- 239000005897 Etoxazole Substances 0.000 claims description 2
- 239000005779 Fenpyrazamine Substances 0.000 claims description 2
- 239000005867 Iprodione Substances 0.000 claims description 2
- 239000005797 Iprovalicarb Substances 0.000 claims description 2
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 claims description 2
- 239000005951 Methiocarb Substances 0.000 claims description 2
- NQRFDNJEBWAUBL-UHFFFAOYSA-N N-[cyano(2-thienyl)methyl]-4-ethyl-2-(ethylamino)-1,3-thiazole-5-carboxamide Chemical compound S1C(NCC)=NC(CC)=C1C(=O)NC(C#N)C1=CC=CS1 NQRFDNJEBWAUBL-UHFFFAOYSA-N 0.000 claims description 2
- YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical compound [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 claims description 2
- 239000005616 Rimsulfuron Substances 0.000 claims description 2
- 239000005664 Spirodiclofen Substances 0.000 claims description 2
- 239000005665 Spiromesifen Substances 0.000 claims description 2
- 239000005931 Spirotetramat Substances 0.000 claims description 2
- 239000005837 Spiroxamine Substances 0.000 claims description 2
- 239000005937 Tebufenozide Substances 0.000 claims description 2
- 239000005939 Tefluthrin Substances 0.000 claims description 2
- 239000005940 Thiacloprid Substances 0.000 claims description 2
- 229930195482 Validamycin Natural products 0.000 claims description 2
- 241000700605 Viruses Species 0.000 claims description 2
- GGKQIOFASHYUJZ-UHFFFAOYSA-N ametoctradin Chemical compound NC1=C(CCCCCCCC)C(CC)=NC2=NC=NN21 GGKQIOFASHYUJZ-UHFFFAOYSA-N 0.000 claims description 2
- BREATYVWRHIPIY-UHFFFAOYSA-N amisulbrom Chemical compound CN(C)S(=O)(=O)N1C=NC(S(=O)(=O)N2C3=CC(F)=CC=C3C(Br)=C2C)=N1 BREATYVWRHIPIY-UHFFFAOYSA-N 0.000 claims description 2
- 229960002587 amitraz Drugs 0.000 claims description 2
- QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical group C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 claims description 2
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 claims description 2
- 229960000686 benzalkonium chloride Drugs 0.000 claims description 2
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 claims description 2
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 claims description 2
- 239000003124 biologic agent Substances 0.000 claims description 2
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- LFHISGNCFUNFFM-UHFFFAOYSA-N chloropicrin Chemical compound [O-][N+](=O)C(Cl)(Cl)Cl LFHISGNCFUNFFM-UHFFFAOYSA-N 0.000 claims description 2
- VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 claims description 2
- 229960003344 climbazole Drugs 0.000 claims description 2
- DVBUIBGJRQBEDP-UHFFFAOYSA-N cyantraniliprole Chemical compound CNC(=O)C1=CC(C#N)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl DVBUIBGJRQBEDP-UHFFFAOYSA-N 0.000 claims description 2
- YXKMMRDKEKCERS-UHFFFAOYSA-N cyazofamid Chemical compound CN(C)S(=O)(=O)N1C(C#N)=NC(Cl)=C1C1=CC=C(C)C=C1 YXKMMRDKEKCERS-UHFFFAOYSA-N 0.000 claims description 2
- APJLTUBHYCOZJI-VZCXRCSSSA-N cyenopyrafen Chemical compound CC1=NN(C)C(\C(OC(=O)C(C)(C)C)=C(/C#N)C=2C=CC(=CC=2)C(C)(C)C)=C1C APJLTUBHYCOZJI-VZCXRCSSSA-N 0.000 claims description 2
- WCMMILVIRZAPLE-UHFFFAOYSA-M cyhexatin Chemical compound C1CCCCC1[Sn](C1CCCCC1)(O)C1CCCCC1 WCMMILVIRZAPLE-UHFFFAOYSA-M 0.000 claims description 2
- 230000000967 entomopathogenic effect Effects 0.000 claims description 2
- DWRKFAJEBUWTQM-UHFFFAOYSA-N etaconazole Chemical compound O1C(CC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 DWRKFAJEBUWTQM-UHFFFAOYSA-N 0.000 claims description 2
- DECIPOUIJURFOJ-UHFFFAOYSA-N ethoxyquin Chemical compound N1C(C)(C)C=C(C)C2=CC(OCC)=CC=C21 DECIPOUIJURFOJ-UHFFFAOYSA-N 0.000 claims description 2
- 229940093500 ethoxyquin Drugs 0.000 claims description 2
- 235000019285 ethoxyquin Nutrition 0.000 claims description 2
- IXSZQYVWNJNRAL-UHFFFAOYSA-N etoxazole Chemical compound CCOC1=CC(C(C)(C)C)=CC=C1C1N=C(C=2C(=CC=CC=2F)F)OC1 IXSZQYVWNJNRAL-UHFFFAOYSA-N 0.000 claims description 2
- XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 claims description 2
- UTOHZQYBSYOOGC-UHFFFAOYSA-N fenpyrazamine Chemical compound O=C1N(C(C)C)N(C(=O)SCC=C)C(N)=C1C1=CC=CC=C1C UTOHZQYBSYOOGC-UHFFFAOYSA-N 0.000 claims description 2
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 claims description 2
- WLPCAERCXQSYLQ-UHFFFAOYSA-N isotianil Chemical compound ClC1=NSC(C(=O)NC=2C(=CC=CC=2)C#N)=C1Cl WLPCAERCXQSYLQ-UHFFFAOYSA-N 0.000 claims description 2
- HYVVJDQGXFXBRZ-UHFFFAOYSA-N metam Chemical compound CNC(S)=S HYVVJDQGXFXBRZ-UHFFFAOYSA-N 0.000 claims description 2
- YFBPRJGDJKVWAH-UHFFFAOYSA-N methiocarb Chemical compound CNC(=O)OC1=CC(C)=C(SC)C(C)=C1 YFBPRJGDJKVWAH-UHFFFAOYSA-N 0.000 claims description 2
- 229940102396 methyl bromide Drugs 0.000 claims description 2
- 229960001952 metrifonate Drugs 0.000 claims description 2
- GIPNVQZZSSKOQF-UHFFFAOYSA-N n'-(2,5-dimethyl-4-phenoxyphenyl)-n-ethyl-n-methylmethanimidamide Chemical compound C1=C(C)C(N=CN(C)CC)=CC(C)=C1OC1=CC=CC=C1 GIPNVQZZSSKOQF-UHFFFAOYSA-N 0.000 claims description 2
- YBQARPUVLHEOSY-UHFFFAOYSA-N n-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-n-[(2-propan-2-ylphenyl)methyl]pyrazole-4-carboxamide Chemical compound CC(C)C1=CC=CC=C1CN(C(=O)C=1C(=NN(C)C=1F)C(F)F)C1CC1 YBQARPUVLHEOSY-UHFFFAOYSA-N 0.000 claims description 2
- 125000005245 nitryl group Chemical group [N+](=O)([O-])* 0.000 claims description 2
- YTYGAJLZOJPJGH-UHFFFAOYSA-N noviflumuron Chemical compound FC1=C(Cl)C(OC(F)(F)C(C(F)(F)F)F)=C(Cl)C=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F YTYGAJLZOJPJGH-UHFFFAOYSA-N 0.000 claims description 2
- 229960000482 pethidine Drugs 0.000 claims description 2
- 235000019260 propionic acid Nutrition 0.000 claims description 2
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 claims description 2
- DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 claims description 2
- CLSVJBIHYWPGQY-GGYDESQDSA-N spirotetramat Chemical compound CCOC(=O)OC1=C(C=2C(=CC=C(C)C=2)C)C(=O)N[C@@]11CC[C@H](OC)CC1 CLSVJBIHYWPGQY-GGYDESQDSA-N 0.000 claims description 2
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 claims description 2
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 claims description 2
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 claims description 2
- WOSNCVAPUOFXEH-UHFFFAOYSA-N thifluzamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=C(Br)C=C(OC(F)(F)F)C=C1Br WOSNCVAPUOFXEH-UHFFFAOYSA-N 0.000 claims description 2
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 claims description 2
- QSOHVSNIQHGFJU-UHFFFAOYSA-L thiosultap disodium Chemical compound [Na+].[Na+].[O-]S(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O QSOHVSNIQHGFJU-UHFFFAOYSA-L 0.000 claims description 2
- VJQYLJSMBWXGDV-UHFFFAOYSA-N tiadinil Chemical compound N1=NSC(C(=O)NC=2C=C(Cl)C(C)=CC=2)=C1C VJQYLJSMBWXGDV-UHFFFAOYSA-N 0.000 claims description 2
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 claims description 2
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 claims description 2
- 241000701447 unidentified baculovirus Species 0.000 claims description 2
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 claims description 2
- 239000005735 Benalaxyl-M Substances 0.000 claims 2
- 239000005808 Metalaxyl-M Substances 0.000 claims 2
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 claims 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 2
- CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 claims 2
- WQOXQRCZOLPYPM-UHFFFAOYSA-N dimethyl disulfide Chemical compound CSSC WQOXQRCZOLPYPM-UHFFFAOYSA-N 0.000 claims 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims 2
- CKJNUZNMWOVDFN-UHFFFAOYSA-N methanone Chemical compound O=[CH-] CKJNUZNMWOVDFN-UHFFFAOYSA-N 0.000 claims 2
- 244000045561 useful plants Species 0.000 claims 2
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 claims 2
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 claims 1
- BKBSMMUEEAWFRX-NBVRZTHBSA-N (E)-flumorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(F)=CC=1)=C\C(=O)N1CCOCC1 BKBSMMUEEAWFRX-NBVRZTHBSA-N 0.000 claims 1
- PVBIWYMFWKOZMN-UHFFFAOYSA-N 1-(5-bromopyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1,2,4-triazol-1-yl)propan-2-ol Chemical compound C=1C=C(F)C=C(F)C=1C(C(F)(F)C=1N=CC(Br)=CC=1)(O)CN1C=NC=N1 PVBIWYMFWKOZMN-UHFFFAOYSA-N 0.000 claims 1
- 125000006426 1-chlorocyclopropyl group Chemical group [H]C1([H])C([H])([H])C1(Cl)* 0.000 claims 1
- NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 claims 1
- GXFIQHWKGLBSLN-UHFFFAOYSA-N 2-benzoxepine Chemical compound O1C=CC=C2C=CC=CC2=C1 GXFIQHWKGLBSLN-UHFFFAOYSA-N 0.000 claims 1
- DHVLDKHFGIVEIP-UHFFFAOYSA-N 2-bromo-2-(bromomethyl)pentanedinitrile Chemical compound BrCC(Br)(C#N)CCC#N DHVLDKHFGIVEIP-UHFFFAOYSA-N 0.000 claims 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 1
- NNWTYSZJLCDUDC-UHFFFAOYSA-N 2-propoxyquinoline Chemical compound C1=CC=CC2=NC(OCCC)=CC=C21 NNWTYSZJLCDUDC-UHFFFAOYSA-N 0.000 claims 1
- RDQSAEZUEUFCFX-UHFFFAOYSA-N 3-methylfuran-2-carboxamide Chemical compound CC=1C=COC=1C(N)=O RDQSAEZUEUFCFX-UHFFFAOYSA-N 0.000 claims 1
- 239000005878 Azadirachtin Substances 0.000 claims 1
- RPSXWXFHCFSWKH-UHFFFAOYSA-N C(CCC)OS(=O)(=O)C1=NC=CC=N1 Chemical compound C(CCC)OS(=O)(=O)C1=NC=CC=N1 RPSXWXFHCFSWKH-UHFFFAOYSA-N 0.000 claims 1
- FTBZZDWKYJXNBN-UHFFFAOYSA-N CN(C1=NN(C=N1)CC1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F)C Chemical compound CN(C1=NN(C=N1)CC1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F)C FTBZZDWKYJXNBN-UHFFFAOYSA-N 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 1
- 239000005756 Cymoxanil Substances 0.000 claims 1
- 239000005644 Dazomet Substances 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 239000005566 Imazamox Substances 0.000 claims 1
- 239000005800 Kresoxim-methyl Substances 0.000 claims 1
- 241000366182 Melaleuca alternifolia Species 0.000 claims 1
- RVUFRLZDOQHZBN-UHFFFAOYSA-N N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide Chemical compound FC(C1=NC(=NO1)C1=CC=C(C=C1)CNC(CC)=O)(F)F RVUFRLZDOQHZBN-UHFFFAOYSA-N 0.000 claims 1
- 239000005823 Propineb Substances 0.000 claims 1
- 239000005929 Spinetoram Substances 0.000 claims 1
- GOENIMGKWNZVDA-OAMCMWGQSA-N Spinetoram Chemical compound CO[C@@H]1[C@H](OCC)[C@@H](OC)[C@H](C)O[C@H]1OC1C[C@H]2[C@@H]3C=C4C(=O)[C@H](C)[C@@H](O[C@@H]5O[C@H](C)[C@H](CC5)N(C)C)CCC[C@H](CC)OC(=O)CC4[C@@H]3CC[C@@H]2C1 GOENIMGKWNZVDA-OAMCMWGQSA-N 0.000 claims 1
- 239000005938 Teflubenzuron Substances 0.000 claims 1
- 241001061127 Thione Species 0.000 claims 1
- 239000005843 Thiram Substances 0.000 claims 1
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 claims 1
- VEHPJKVTJQSSKL-UHFFFAOYSA-N azadirachtin Natural products O1C2(C)C(C3(C=COC3O3)O)CC3C21C1(C)C(O)C(OCC2(OC(C)=O)C(CC3OC(=O)C(C)=CC)OC(C)=O)C2C32COC(C(=O)OC)(O)C12 VEHPJKVTJQSSKL-UHFFFAOYSA-N 0.000 claims 1
- FTNJWQUOZFUQQJ-NDAWSKJSSA-N azadirachtin A Chemical compound C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C\C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-NDAWSKJSSA-N 0.000 claims 1
- FTNJWQUOZFUQQJ-IRYYUVNJSA-N azadirachtin A Natural products C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C/C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-IRYYUVNJSA-N 0.000 claims 1
- CWFOCCVIPCEQCK-UHFFFAOYSA-N chlorfenapyr Chemical compound BrC1=C(C(F)(F)F)N(COCC)C(C=2C=CC(Cl)=CC=2)=C1C#N CWFOCCVIPCEQCK-UHFFFAOYSA-N 0.000 claims 1
- 229940109275 cyclamate Drugs 0.000 claims 1
- HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical compound OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 claims 1
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 claims 1
- WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 claims 1
- WHDGWKAJBYRJJL-UHFFFAOYSA-K ferbam Chemical compound [Fe+3].CN(C)C([S-])=S.CN(C)C([S-])=S.CN(C)C([S-])=S WHDGWKAJBYRJJL-UHFFFAOYSA-K 0.000 claims 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims 1
- 229910052737 gold Inorganic materials 0.000 claims 1
- 239000010931 gold Substances 0.000 claims 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 claims 1
- UFHLMYOGRXOCSL-UHFFFAOYSA-N isoprothiolane Chemical compound CC(C)OC(=O)C(C(=O)OC(C)C)=C1SCCS1 UFHLMYOGRXOCSL-UHFFFAOYSA-N 0.000 claims 1
- ZOTBXTZVPHCKPN-HTXNQAPBSA-N kresoxim-methyl Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1C ZOTBXTZVPHCKPN-HTXNQAPBSA-N 0.000 claims 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 claims 1
- 229920000940 maneb Polymers 0.000 claims 1
- RPJOONIASVZOKB-UHFFFAOYSA-N n-ethyl-n-methylmethanimidamide Chemical compound CCN(C)C=N RPJOONIASVZOKB-UHFFFAOYSA-N 0.000 claims 1
- 229940038580 oat bran Drugs 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- 239000000419 plant extract Substances 0.000 claims 1
- 150000004672 propanoic acids Chemical class 0.000 claims 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 claims 1
- FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 claims 1
- 229960002026 pyrithione Drugs 0.000 claims 1
- FKENQMMABCRJMK-RITPCOANSA-N sulbactam Chemical compound O=S1(=O)C(C)(C)[C@H](C(O)=O)N2C(=O)C[C@H]21 FKENQMMABCRJMK-RITPCOANSA-N 0.000 claims 1
- 229960005256 sulbactam Drugs 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 claims 1
- 229960002447 thiram Drugs 0.000 claims 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 claims 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 claims 1
- 229960003500 triclosan Drugs 0.000 claims 1
- 244000005700 microbiome Species 0.000 abstract description 7
- 206010061217 Infestation Diseases 0.000 abstract description 5
- 238000003898 horticulture Methods 0.000 abstract description 2
- 241000196324 Embryophyta Species 0.000 description 79
- 241000682645 Phakopsora pachyrhizi Species 0.000 description 48
- 230000000694 effects Effects 0.000 description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 30
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 29
- 238000012360 testing method Methods 0.000 description 28
- 244000068988 Glycine max Species 0.000 description 26
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 25
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 24
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 22
- 239000000243 solution Substances 0.000 description 21
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 19
- 239000003921 oil Substances 0.000 description 18
- 235000019198 oils Nutrition 0.000 description 18
- 230000002195 synergetic effect Effects 0.000 description 16
- 235000010469 Glycine max Nutrition 0.000 description 15
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 15
- 238000011282 treatment Methods 0.000 description 15
- 241000607479 Yersinia pestis Species 0.000 description 14
- 238000011161 development Methods 0.000 description 14
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 13
- 239000005667 attractant Substances 0.000 description 13
- 230000001276 controlling effect Effects 0.000 description 13
- 230000018109 developmental process Effects 0.000 description 13
- 230000002538 fungal effect Effects 0.000 description 13
- PEHIOOIMFRIBHM-UHFFFAOYSA-N 3-[2-(1-chlorocyclopropyl)-3-(2-fluorophenyl)-2-hydroxypropyl]imidazole-4-carbonitrile Chemical compound ClC1(CC1)C(CN1C=NC=C1C#N)(CC1=C(C=CC=C1)F)O PEHIOOIMFRIBHM-UHFFFAOYSA-N 0.000 description 12
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 239000005558 Fluroxypyr Substances 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 241000209140 Triticum Species 0.000 description 12
- 235000021307 Triticum Nutrition 0.000 description 12
- 230000031902 chemoattractant activity Effects 0.000 description 12
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 description 12
- 230000002829 reductive effect Effects 0.000 description 12
- 239000007787 solid Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- 239000000725 suspension Substances 0.000 description 12
- 241000228143 Penicillium Species 0.000 description 11
- 241000221300 Puccinia Species 0.000 description 11
- 239000004202 carbamide Substances 0.000 description 11
- 244000038559 crop plants Species 0.000 description 11
- 235000019439 ethyl acetate Nutrition 0.000 description 11
- 239000003112 inhibitor Substances 0.000 description 11
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 11
- PDPWCKVFIFAQIQ-UHFFFAOYSA-N 2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide Chemical compound CNC(=O)C(OC)C1=CC=CC=C1COC1=CC(C)=CC=C1C PDPWCKVFIFAQIQ-UHFFFAOYSA-N 0.000 description 10
- 239000005803 Mandestrobin Substances 0.000 description 10
- 241000579741 Sphaerotheca <fungi> Species 0.000 description 10
- 230000012010 growth Effects 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 10
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 10
- 229940080818 propionamide Drugs 0.000 description 10
- CRFYLQMIDWBKRT-LPYMAVHISA-N pyribencarb Chemical compound C1=C(Cl)C(CNC(=O)OC)=CC(C(\C)=N\OCC=2N=C(C)C=CC=2)=C1 CRFYLQMIDWBKRT-LPYMAVHISA-N 0.000 description 10
- 230000035882 stress Effects 0.000 description 10
- 241000223600 Alternaria Species 0.000 description 9
- 244000105624 Arachis hypogaea Species 0.000 description 9
- 241000221535 Pucciniales Species 0.000 description 9
- 238000010790 dilution Methods 0.000 description 9
- 239000012895 dilution Substances 0.000 description 9
- 235000013399 edible fruits Nutrition 0.000 description 9
- 230000006872 improvement Effects 0.000 description 9
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 9
- JHIPUJPTQJYEQK-ZLHHXESBSA-N orysastrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1CO\N=C(/C)\C(=N\OC)\C(\C)=N\OC JHIPUJPTQJYEQK-ZLHHXESBSA-N 0.000 description 9
- 238000003860 storage Methods 0.000 description 9
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 9
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 8
- 241000233679 Peronosporaceae Species 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 238000011534 incubation Methods 0.000 description 8
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 description 8
- XUQQRGKFXLAPNV-UHFFFAOYSA-N metyltetraprole Chemical compound CC1=CC=CC(N2C(N(C)N=N2)=O)=C1COC(=N1)C=CN1C1=CC=C(Cl)C=C1 XUQQRGKFXLAPNV-UHFFFAOYSA-N 0.000 description 8
- 238000003359 percent control normalization Methods 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical group [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 239000003053 toxin Substances 0.000 description 8
- 231100000765 toxin Toxicity 0.000 description 8
- 108700012359 toxins Proteins 0.000 description 8
- QFNFRZHOXWNWAQ-UHFFFAOYSA-N triclopyricarb Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NC(Cl)=C(Cl)C=C1Cl QFNFRZHOXWNWAQ-UHFFFAOYSA-N 0.000 description 8
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 8
- 235000013311 vegetables Nutrition 0.000 description 8
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 7
- 235000010777 Arachis hypogaea Nutrition 0.000 description 7
- 239000005777 Fenpropidin Substances 0.000 description 7
- 241000233614 Phytophthora Species 0.000 description 7
- 241001533598 Septoria Species 0.000 description 7
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 7
- 230000009471 action Effects 0.000 description 7
- 239000000654 additive Substances 0.000 description 7
- 230000004071 biological effect Effects 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 7
- SYTBZMRGLBWNTM-UHFFFAOYSA-N flurbiprofen Chemical compound FC1=CC(C(C(O)=O)C)=CC=C1C1=CC=CC=C1 SYTBZMRGLBWNTM-UHFFFAOYSA-N 0.000 description 7
- 229960002390 flurbiprofen Drugs 0.000 description 7
- 125000000524 functional group Chemical group 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- 229920006395 saturated elastomer Polymers 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 241000894007 species Species 0.000 description 7
- 238000001228 spectrum Methods 0.000 description 7
- 241000223218 Fusarium Species 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 6
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 6
- 235000002634 Solanum Nutrition 0.000 description 6
- 241000207763 Solanum Species 0.000 description 6
- 241001480238 Steinernema Species 0.000 description 6
- 239000013543 active substance Substances 0.000 description 6
- 150000001336 alkenes Chemical class 0.000 description 6
- 235000013339 cereals Nutrition 0.000 description 6
- 238000006880 cross-coupling reaction Methods 0.000 description 6
- 239000004009 herbicide Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 6
- 230000017066 negative regulation of growth Effects 0.000 description 6
- 235000020232 peanut Nutrition 0.000 description 6
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 description 6
- 239000001965 potato dextrose agar Substances 0.000 description 6
- 108090000623 proteins and genes Proteins 0.000 description 6
- 235000000346 sugar Nutrition 0.000 description 6
- 230000009466 transformation Effects 0.000 description 6
- 239000003643 water by type Substances 0.000 description 6
- 239000002023 wood Substances 0.000 description 6
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 description 5
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 5
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 5
- 229920001817 Agar Polymers 0.000 description 5
- 241000123650 Botrytis cinerea Species 0.000 description 5
- 241000222235 Colletotrichum orbiculare Species 0.000 description 5
- 239000005778 Fenpropimorph Substances 0.000 description 5
- 239000005781 Fludioxonil Substances 0.000 description 5
- 239000005789 Folpet Substances 0.000 description 5
- 241000131448 Mycosphaerella Species 0.000 description 5
- 241001123569 Puccinia recondita Species 0.000 description 5
- 241000233639 Pythium Species 0.000 description 5
- 241000235527 Rhizopus Species 0.000 description 5
- 241001558929 Sclerotium <basidiomycota> Species 0.000 description 5
- 241001360088 Zymoseptoria tritici Species 0.000 description 5
- 239000008272 agar Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000012267 brine Substances 0.000 description 5
- 230000002349 favourable effect Effects 0.000 description 5
- 239000003337 fertilizer Substances 0.000 description 5
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 description 5
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 5
- 238000011081 inoculation Methods 0.000 description 5
- 239000003094 microcapsule Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 102000004169 proteins and genes Human genes 0.000 description 5
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- 239000012085 test solution Substances 0.000 description 5
- 230000001225 therapeutic effect Effects 0.000 description 5
- 238000000844 transformation Methods 0.000 description 5
- 230000009261 transgenic effect Effects 0.000 description 5
- UOORRWUZONOOLO-OWOJBTEDSA-N (E)-1,3-dichloropropene Chemical compound ClC\C=C\Cl UOORRWUZONOOLO-OWOJBTEDSA-N 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 4
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 description 4
- QXDOFVVNXBGLKK-UHFFFAOYSA-N 3-Isoxazolidinone Chemical compound OC1=NOCC1 QXDOFVVNXBGLKK-UHFFFAOYSA-N 0.000 description 4
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 4
- 241001124076 Aphididae Species 0.000 description 4
- 235000017060 Arachis glabrata Nutrition 0.000 description 4
- 235000018262 Arachis monticola Nutrition 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- 241000222199 Colletotrichum Species 0.000 description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 241000221787 Erysiphe Species 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical compound OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 241000308375 Graminicola Species 0.000 description 4
- 241000235395 Mucor Species 0.000 description 4
- 241000315044 Passalora arachidicola Species 0.000 description 4
- 239000002202 Polyethylene glycol Chemical class 0.000 description 4
- 241001092489 Potentilla Species 0.000 description 4
- 241001597349 Septoria glycines Species 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
- 229910052794 bromium Inorganic materials 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 4
- 229960001231 choline Drugs 0.000 description 4
- BSEXNZMHLUMQKR-UHFFFAOYSA-N cyclopropanecarboxamide Chemical compound NC(=O)C1CC1.NC(=O)C1CC1 BSEXNZMHLUMQKR-UHFFFAOYSA-N 0.000 description 4
- 238000004807 desolvation Methods 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 238000003818 flash chromatography Methods 0.000 description 4
- 235000019253 formic acid Nutrition 0.000 description 4
- 150000004820 halides Chemical class 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 4
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 4
- KZCSJNBXJOCZEG-XFFZJAGNSA-N methyl (Z)-2-(5-bromo-2-methylphenoxy)-3-methoxyprop-2-enoate Chemical compound BrC=1C=CC(=C(O\C(\C(=O)OC)=C/OC)C=1)C KZCSJNBXJOCZEG-XFFZJAGNSA-N 0.000 description 4
- GTCAXTIRRLKXRU-UHFFFAOYSA-N methyl carbamate Chemical compound COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920001223 polyethylene glycol Chemical class 0.000 description 4
- 229910000027 potassium carbonate Chemical group 0.000 description 4
- 229910000160 potassium phosphate Inorganic materials 0.000 description 4
- 235000011009 potassium phosphates Nutrition 0.000 description 4
- 230000003449 preventive effect Effects 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 125000002577 pseudohalo group Chemical group 0.000 description 4
- 239000003128 rodenticide Substances 0.000 description 4
- UOORRWUZONOOLO-UHFFFAOYSA-N telone II Natural products ClCC=CCl UOORRWUZONOOLO-UHFFFAOYSA-N 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- 238000004704 ultra performance liquid chromatography Methods 0.000 description 4
- 235000020234 walnut Nutrition 0.000 description 4
- RMOGWMIKYWRTKW-UONOGXRCSA-N (S,S)-paclobutrazol Chemical compound C([C@@H]([C@@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1 RMOGWMIKYWRTKW-UONOGXRCSA-N 0.000 description 3
- XEJNEDVTJPXRSM-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-5-methyl-4,5-dihydro-1H-pyrazole-3,5-dicarboxylic acid Chemical compound OC(=O)C1(C)CC(C(O)=O)=NN1C1=CC=C(Cl)C=C1Cl XEJNEDVTJPXRSM-UHFFFAOYSA-N 0.000 description 3
- 241000235349 Ascomycota Species 0.000 description 3
- 241000221198 Basidiomycota Species 0.000 description 3
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- 241001290235 Ceratobasidium cereale Species 0.000 description 3
- 241001157813 Cercospora Species 0.000 description 3
- 240000008067 Cucumis sativus Species 0.000 description 3
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 3
- 241000235819 Cytospora Species 0.000 description 3
- 241001273416 Didymella arachidicola Species 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 3
- 240000007049 Juglans regia Species 0.000 description 3
- 235000009496 Juglans regia Nutrition 0.000 description 3
- 241001518731 Monilinia fructicola Species 0.000 description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 3
- 241001134446 Niveas Species 0.000 description 3
- 241000233654 Oomycetes Species 0.000 description 3
- 239000005985 Paclobutrazol Substances 0.000 description 3
- 241001223281 Peronospora Species 0.000 description 3
- 241000233631 Phytophthora citrophthora Species 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 239000005820 Prochloraz Substances 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 241000899394 Pseudocercospora Species 0.000 description 3
- 241001123583 Puccinia striiformis Species 0.000 description 3
- 241000221662 Sclerotinia Species 0.000 description 3
- 244000062793 Sorghum vulgare Species 0.000 description 3
- 241000219315 Spinacia Species 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 239000005847 Triazoxide Substances 0.000 description 3
- 241000223259 Trichoderma Species 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 230000036579 abiotic stress Effects 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 125000005907 alkyl ester group Chemical group 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 239000004490 capsule suspension Substances 0.000 description 3
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 3
- 229950001327 dichlorvos Drugs 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 230000003631 expected effect Effects 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 235000013312 flour Nutrition 0.000 description 3
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 3
- 230000035784 germination Effects 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 238000003306 harvesting Methods 0.000 description 3
- 208000015181 infectious disease Diseases 0.000 description 3
- 239000002418 insect attractant Substances 0.000 description 3
- 238000009630 liquid culture Methods 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229910052752 metalloid Inorganic materials 0.000 description 3
- 150000002738 metalloids Chemical class 0.000 description 3
- 239000011785 micronutrient Substances 0.000 description 3
- 235000013369 micronutrients Nutrition 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 230000035772 mutation Effects 0.000 description 3
- JEFUQUGZXLEHLD-UHFFFAOYSA-N n-[(5-chloro-2-propan-2-ylphenyl)methyl]-n-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1=CC=C(Cl)C=C1CN(C(=O)C=1C(=NN(C)C=1F)C(F)F)C1CC1 JEFUQUGZXLEHLD-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 235000016709 nutrition Nutrition 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000000361 pesticidal effect Effects 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 239000003016 pheromone Substances 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 3
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 239000004546 suspension concentrate Substances 0.000 description 3
- 230000009044 synergistic interaction Effects 0.000 description 3
- 230000009885 systemic effect Effects 0.000 description 3
- 239000004557 technical material Substances 0.000 description 3
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 3
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 3
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 3
- CYPYTURSJDMMMP-WVCUSYJESA-N (1e,4e)-1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 CYPYTURSJDMMMP-WVCUSYJESA-N 0.000 description 2
- JTBBRGSSVACAJM-UHFFFAOYSA-N (2-methyl-2,3-dihydro-1-benzofuran-7-yl) n-methylcarbamate Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)C2 JTBBRGSSVACAJM-UHFFFAOYSA-N 0.000 description 2
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 2
- PWWPULQZEAPTTB-UHFFFAOYSA-N (4-phenoxyphenyl)methyl 2-amino-6-methylpyridine-3-carboxylate Chemical compound NC1=NC(C)=CC=C1C(=O)OCC(C=C1)=CC=C1OC1=CC=CC=C1 PWWPULQZEAPTTB-UHFFFAOYSA-N 0.000 description 2
- NHMKYUHMPXBMFI-SNVBAGLBSA-N (4s)-2-methyl-6-methylideneocta-2,7-dien-4-ol Chemical compound CC(C)=C[C@@H](O)CC(=C)C=C NHMKYUHMPXBMFI-SNVBAGLBSA-N 0.000 description 2
- GBFKIHJZPMECCF-BXUZGUMPSA-N (R,R)-cyclobutrifluram Chemical compound FC(F)(F)C1=NC=CC=C1C(=O)N[C@H]1[C@@H](C=2C(=CC(Cl)=CC=2)Cl)CC1 GBFKIHJZPMECCF-BXUZGUMPSA-N 0.000 description 2
- XBCKTJDKWPZLJH-ZUPCBTBPSA-N (z,2e)-5-[1-(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-n,3-dimethylpent-3-enamide Chemical compound N1=C(OC\C=C(\C)/C(=N\OC)/C(=O)NC)C=CN1C1=CC=C(Cl)C=C1 XBCKTJDKWPZLJH-ZUPCBTBPSA-N 0.000 description 2
- KZPYGQFFRCFCPP-UHFFFAOYSA-N 1,1'-bis(diphenylphosphino)ferrocene Chemical compound [Fe+2].C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1 KZPYGQFFRCFCPP-UHFFFAOYSA-N 0.000 description 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- IAQLCKZJGNTRDO-UHFFFAOYSA-N 1-(4-{4-[5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone Chemical compound CC1=CC(C(F)(F)F)=NN1CC(=O)N1CCC(C=2SC=C(N=2)C=2CC(ON=2)C=2C(=CC=CC=2F)F)CC1 IAQLCKZJGNTRDO-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 description 2
- IBYHHJPAARCAIE-UHFFFAOYSA-N 1-bromo-2-chloroethane Chemical compound ClCCBr IBYHHJPAARCAIE-UHFFFAOYSA-N 0.000 description 2
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 description 2
- MTJLFBYYTSWTBO-UHFFFAOYSA-N 1-fluoropiperidine Chemical compound FN1CCCCC1 MTJLFBYYTSWTBO-UHFFFAOYSA-N 0.000 description 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
- GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 description 2
- SIIJJFOXEOHODQ-UHFFFAOYSA-N 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-3-methyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C=1C=C(OC=2C=CC(Cl)=CC=2)C=C(C(F)(F)F)C=1C(O)(C(C)C)CN1C=NC=N1 SIIJJFOXEOHODQ-UHFFFAOYSA-N 0.000 description 2
- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
- FSCWZHGZWWDELK-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-5-ethenyl-5-methyl-2,4-oxazolidinedione Chemical compound O=C1C(C)(C=C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FSCWZHGZWWDELK-UHFFFAOYSA-N 0.000 description 2
- XCGBHLLWJZOLEM-UHFFFAOYSA-N 3-(difluoromethyl)-N-(7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1-methyl-1H-pyrazole-4-carboxamide Chemical compound CC1CC(C)(C)C(C(=CC=2)F)=C1C=2NC(=O)C1=CN(C)N=C1C(F)F XCGBHLLWJZOLEM-UHFFFAOYSA-N 0.000 description 2
- 229940099451 3-iodo-2-propynylbutylcarbamate Drugs 0.000 description 2
- SWTPIYGGSMJRTB-UHFFFAOYSA-N 4,4-difluoro-3,3-dimethyl-1-quinolin-3-ylisoquinoline Chemical compound C12=CC=CC=C2C(F)(F)C(C)(C)N=C1C1=CN=C(C=CC=C2)C2=C1 SWTPIYGGSMJRTB-UHFFFAOYSA-N 0.000 description 2
- BQMRHYBXRAYYQS-UHFFFAOYSA-N 4-dihydroxyphosphinothioyloxy-n,n-diethyl-6-methylpyrimidin-2-amine Chemical compound CCN(CC)C1=NC(C)=CC(OP(O)(O)=S)=N1 BQMRHYBXRAYYQS-UHFFFAOYSA-N 0.000 description 2
- VTUFOIHYMMMNOM-VOTSOKGWSA-N 5E-Decenyl acetate Chemical compound CCCC\C=C\CCCCOC(C)=O VTUFOIHYMMMNOM-VOTSOKGWSA-N 0.000 description 2
- 239000005964 Acibenzolar-S-methyl Substances 0.000 description 2
- 240000002234 Allium sativum Species 0.000 description 2
- 241000213004 Alternaria solani Species 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- 241001600407 Aphis <genus> Species 0.000 description 2
- 235000003276 Apios tuberosa Nutrition 0.000 description 2
- 235000010744 Arachis villosulicarpa Nutrition 0.000 description 2
- 244000075850 Avena orientalis Species 0.000 description 2
- 235000007319 Avena orientalis Nutrition 0.000 description 2
- 241000193738 Bacillus anthracis Species 0.000 description 2
- 239000005734 Benalaxyl Substances 0.000 description 2
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 2
- 239000002028 Biomass Substances 0.000 description 2
- 241000760381 Blastocladiomycetes Species 0.000 description 2
- 241000130841 Blumeriella jaapii Species 0.000 description 2
- 241001465180 Botrytis Species 0.000 description 2
- HCEJRQCEFIFCOZ-UHFFFAOYSA-N BrC=1C=C(C(=NC1OC(COCCC)C)C)N=CN(C)CC Chemical compound BrC=1C=C(C(=NC1OC(COCCC)C)C)N=CN(C)CC HCEJRQCEFIFCOZ-UHFFFAOYSA-N 0.000 description 2
- HCEJRQCEFIFCOZ-GFCCVEGCSA-N BrC=1C=C(C(=NC=1O[C@@H](COCCC)C)C)N=CN(C)CC Chemical compound BrC=1C=C(C(=NC=1O[C@@H](COCCC)C)C)N=CN(C)CC HCEJRQCEFIFCOZ-GFCCVEGCSA-N 0.000 description 2
- 241000219198 Brassica Species 0.000 description 2
- 240000007124 Brassica oleracea Species 0.000 description 2
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 2
- 239000005742 Bupirimate Substances 0.000 description 2
- LMZXCAKAGHEUDK-JOCHJYFZSA-N C1=C(C2=NC=C(C=C2C=C1)C(=O)N[C@](CC(=C)Cl)(CC1=CC=CC=C1)C)F Chemical compound C1=C(C2=NC=C(C=C2C=C1)C(=O)N[C@](CC(=C)Cl)(CC1=CC=CC=C1)C)F LMZXCAKAGHEUDK-JOCHJYFZSA-N 0.000 description 2
- OOMJEEDFRHYBHE-UHFFFAOYSA-N COC(C(=CO)OC1=C(C=CC(=C1)Br)C)=O Chemical compound COC(C(=CO)OC1=C(C=CC(=C1)Br)C)=O OOMJEEDFRHYBHE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 239000005745 Captan Substances 0.000 description 2
- 239000005746 Carboxin Substances 0.000 description 2
- 241000221955 Chaetomium Species 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241000207199 Citrus Species 0.000 description 2
- MXQAQBVQVICYFU-UHFFFAOYSA-N ClC=1C=C(C(=NC=1OC(COCCC)C)C)N=CN(C)CC Chemical compound ClC=1C=C(C(=NC=1OC(COCCC)C)C)N=CN(C)CC MXQAQBVQVICYFU-UHFFFAOYSA-N 0.000 description 2
- 241000222290 Cladosporium Species 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000005752 Copper oxychloride Substances 0.000 description 2
- 235000007466 Corylus avellana Nutrition 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 241001337994 Cryptococcus <scale insect> Species 0.000 description 2
- 241001306390 Diaporthe ampelina Species 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- 241001116742 Drynaria Species 0.000 description 2
- 239000005769 Etridiazole Substances 0.000 description 2
- PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 description 2
- 239000005782 Fluopicolide Substances 0.000 description 2
- 239000005786 Flutolanil Substances 0.000 description 2
- 239000005790 Fosetyl Substances 0.000 description 2
- 240000009088 Fragaria x ananassa Species 0.000 description 2
- 241000223195 Fusarium graminearum Species 0.000 description 2
- 241000223221 Fusarium oxysporum Species 0.000 description 2
- 235000018958 Gardenia augusta Nutrition 0.000 description 2
- 241000159512 Geotrichum Species 0.000 description 2
- 206010018498 Goitre Diseases 0.000 description 2
- 244000299507 Gossypium hirsutum Species 0.000 description 2
- 235000003222 Helianthus annuus Nutrition 0.000 description 2
- 241001181537 Hemileia Species 0.000 description 2
- 241001523412 Heterorhabditis bacteriophora Species 0.000 description 2
- 101000858267 Homo sapiens Cytochrome b Proteins 0.000 description 2
- 241000143667 Hypocrella Species 0.000 description 2
- NHMKYUHMPXBMFI-UHFFFAOYSA-N Ipsdienol-d Natural products CC(C)=CC(O)CC(=C)C=C NHMKYUHMPXBMFI-UHFFFAOYSA-N 0.000 description 2
- 241000188153 Isaria fumosorosea Species 0.000 description 2
- 239000005908 Isaria fumosorosea Apopka strain 97 (formely Paecilomyces fumosoroseus) Substances 0.000 description 2
- 235000003228 Lactuca sativa Nutrition 0.000 description 2
- 240000008415 Lactuca sativa Species 0.000 description 2
- 102100021695 Lanosterol 14-alpha demethylase Human genes 0.000 description 2
- 101710146773 Lanosterol 14-alpha demethylase Proteins 0.000 description 2
- 241000227653 Lycopersicon Species 0.000 description 2
- 241000193386 Lysinibacillus sphaericus Species 0.000 description 2
- 235000011430 Malus pumila Nutrition 0.000 description 2
- 235000015103 Malus silvestris Nutrition 0.000 description 2
- 241001646834 Mesona Species 0.000 description 2
- FLIACVVOZYBSBS-UHFFFAOYSA-N Methyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC FLIACVVOZYBSBS-UHFFFAOYSA-N 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- 241000226677 Myceliophthora Species 0.000 description 2
- FTCOKXNKPOUEFH-UHFFFAOYSA-N Myclozolin Chemical compound O=C1C(COC)(C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FTCOKXNKPOUEFH-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- SHULZDWNYHRQNK-UHFFFAOYSA-N N-[(E)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide Chemical compound CO\N=C/NC(=O)C1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F SHULZDWNYHRQNK-UHFFFAOYSA-N 0.000 description 2
- LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 description 2
- XQJQCBDIXRIYRP-UHFFFAOYSA-N N-{2-[1,1'-bi(cyclopropyl)-2-yl]phenyl}-3-(difluoromethyl)-1-methyl-1pyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1C(C2CC2)C1 XQJQCBDIXRIYRP-UHFFFAOYSA-N 0.000 description 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 2
- 241000256259 Noctuidae Species 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 239000005812 Oxathiapiprolin Substances 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000005814 Pencycuron Substances 0.000 description 2
- 244000025272 Persea americana Species 0.000 description 2
- 235000008673 Persea americana Nutrition 0.000 description 2
- 241000199919 Phaeophyceae Species 0.000 description 2
- 241001503951 Phoma Species 0.000 description 2
- 241001480007 Phomopsis Species 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 241001130943 Phyllanthus <Aves> Species 0.000 description 2
- 241000172199 Phyllospora Species 0.000 description 2
- 241000233622 Phytophthora infestans Species 0.000 description 2
- 241000179202 Phytoseiulus Species 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 241000222350 Pleurotus Species 0.000 description 2
- 241000221945 Podospora Species 0.000 description 2
- 229930182764 Polyoxin Natural products 0.000 description 2
- 229920001213 Polysorbate 20 Polymers 0.000 description 2
- 241001544359 Polyspora Species 0.000 description 2
- 241000343500 Puccinia arachidis Species 0.000 description 2
- 239000005829 Pyriofenone Substances 0.000 description 2
- 239000005927 Pyriproxyfen Substances 0.000 description 2
- 239000005831 Quinoxyfen Substances 0.000 description 2
- 101150090155 R gene Proteins 0.000 description 2
- 241000959624 Ramaria Species 0.000 description 2
- 241000813090 Rhizoctonia solani Species 0.000 description 2
- 244000068437 Rhizophora sp Species 0.000 description 2
- 241000342322 Sclerospora graminicola Species 0.000 description 2
- 241000221696 Sclerotinia sclerotiorum Species 0.000 description 2
- 239000005834 Sedaxane Substances 0.000 description 2
- 235000005775 Setaria Nutrition 0.000 description 2
- 241000232088 Setaria <nematode> Species 0.000 description 2
- 239000000877 Sex Attractant Substances 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 2
- 229930182558 Sterol Natural products 0.000 description 2
- 102000019259 Succinate Dehydrogenase Human genes 0.000 description 2
- 108010012901 Succinate Dehydrogenase Proteins 0.000 description 2
- 241001122767 Theaceae Species 0.000 description 2
- 240000006474 Theobroma bicolor Species 0.000 description 2
- 239000005842 Thiophanate-methyl Substances 0.000 description 2
- FOCVUCIESVLUNU-UHFFFAOYSA-N Thiotepa Chemical compound C1CN1P(N1CC1)(=S)N1CC1 FOCVUCIESVLUNU-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 241000983470 Typhula ishikariensis Species 0.000 description 2
- 235000015919 Ustilago maydis Nutrition 0.000 description 2
- 244000301083 Ustilago maydis Species 0.000 description 2
- 241000233791 Ustilago tritici Species 0.000 description 2
- 244000078534 Vaccinium myrtillus Species 0.000 description 2
- 241000082085 Verticillium <Phyllachorales> Species 0.000 description 2
- 235000014787 Vitis vinifera Nutrition 0.000 description 2
- 240000006365 Vitis vinifera Species 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical group CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229940100198 alkylating agent Drugs 0.000 description 2
- 239000002168 alkylating agent Substances 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 230000000843 anti-fungal effect Effects 0.000 description 2
- 230000000433 anti-nutritional effect Effects 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 235000021028 berry Nutrition 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- YNHIGQDRGKUECZ-UHFFFAOYSA-L bis(triphenylphosphine)palladium(ii) dichloride Chemical compound [Cl-].[Cl-].[Pd+2].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 description 2
- 238000009395 breeding Methods 0.000 description 2
- QSLZKWPYTWEWHC-UHFFFAOYSA-N broflanilide Chemical compound C=1C=CC(C(=O)NC=2C(=CC(=CC=2Br)C(F)(C(F)(F)F)C(F)(F)F)C(F)(F)F)=C(F)C=1N(C)C(=O)C1=CC=CC=C1 QSLZKWPYTWEWHC-UHFFFAOYSA-N 0.000 description 2
- 230000028446 budding cell bud growth Effects 0.000 description 2
- DSKJPMWIHSOYEA-UHFFFAOYSA-N bupirimate Chemical compound CCCCC1=C(C)N=C(NCC)N=C1OS(=O)(=O)N(C)C DSKJPMWIHSOYEA-UHFFFAOYSA-N 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 229940117949 captan Drugs 0.000 description 2
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 2
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 description 2
- 235000020971 citrus fruits Nutrition 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000002860 competitive effect Effects 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 230000017858 demethylation Effects 0.000 description 2
- 238000010520 demethylation reaction Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003937 drug carrier Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 238000003821 enantio-separation Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- BBXXLROWFHWFQY-UHFFFAOYSA-N ethirimol Chemical compound CCCCC1=C(C)NC(NCC)=NC1=O BBXXLROWFHWFQY-UHFFFAOYSA-N 0.000 description 2
- KQTVWCSONPJJPE-UHFFFAOYSA-N etridiazole Chemical compound CCOC1=NC(C(Cl)(Cl)Cl)=NS1 KQTVWCSONPJJPE-UHFFFAOYSA-N 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- 238000000105 evaporative light scattering detection Methods 0.000 description 2
- RBWGTZRSEOIHFD-UHUFKFKFSA-N fenaminstrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1CO\N=C(/C)\C=C\C1=C(Cl)C=CC=C1Cl RBWGTZRSEOIHFD-UHUFKFKFSA-N 0.000 description 2
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 2
- GBOYJIHYACSLGN-UHFFFAOYSA-N fluopicolide Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CNC(=O)C1=C(Cl)C=CC=C1Cl GBOYJIHYACSLGN-UHFFFAOYSA-N 0.000 description 2
- GNVDAZSPJWCIQZ-UHFFFAOYSA-N flusulfamide Chemical compound ClC1=CC([N+](=O)[O-])=CC=C1NS(=O)(=O)C1=CC=C(Cl)C(C(F)(F)F)=C1 GNVDAZSPJWCIQZ-UHFFFAOYSA-N 0.000 description 2
- PTCGDEVVHUXTMP-UHFFFAOYSA-N flutolanil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C(F)(F)F)=C1 PTCGDEVVHUXTMP-UHFFFAOYSA-N 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000010353 genetic engineering Methods 0.000 description 2
- IXORZMNAPKEEDV-UHFFFAOYSA-N gibberellic acid GA3 Natural products OC(=O)C1C2(C3)CC(=C)C3(O)CCC2C2(C=CC3O)C1C3(C)C(=O)O2 IXORZMNAPKEEDV-UHFFFAOYSA-N 0.000 description 2
- 201000003872 goiter Diseases 0.000 description 2
- 230000007407 health benefit Effects 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 239000004047 hole gas Substances 0.000 description 2
- 238000009905 homogeneous catalytic hydrogenation reaction Methods 0.000 description 2
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 description 2
- 230000036039 immunity Effects 0.000 description 2
- YTCIYOXHHQLDEI-SNVBAGLBSA-N inpyrfluxam Chemical compound C([C@H](C=12)C)C(C)(C)C2=CC=CC=1NC(=O)C1=CN(C)N=C1C(F)F YTCIYOXHHQLDEI-SNVBAGLBSA-N 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- HDHLIWCXDDZUFH-UHFFFAOYSA-N irgarol 1051 Chemical compound CC(C)(C)NC1=NC(SC)=NC(NC2CC2)=N1 HDHLIWCXDDZUFH-UHFFFAOYSA-N 0.000 description 2
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 230000002147 killing effect Effects 0.000 description 2
- 230000002045 lasting effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- UKWHYYKOEPRTIC-UHFFFAOYSA-N mercury(ii) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- AFCCDDWKHLHPDF-UHFFFAOYSA-M metam-sodium Chemical compound [Na+].CNC([S-])=S AFCCDDWKHLHPDF-UHFFFAOYSA-M 0.000 description 2
- AAIZRAWRPZJFAN-UHFFFAOYSA-N methyl 2-(5-bromo-2-methylphenoxy)acetate Chemical compound COC(=O)COc1cc(Br)ccc1C AAIZRAWRPZJFAN-UHFFFAOYSA-N 0.000 description 2
- YDCHPLOFQATIDS-UHFFFAOYSA-N methyl 2-bromoacetate Chemical compound COC(=O)CBr YDCHPLOFQATIDS-UHFFFAOYSA-N 0.000 description 2
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 2
- 230000000813 microbial effect Effects 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 239000005445 natural material Substances 0.000 description 2
- LQERIDTXQFOHKA-UHFFFAOYSA-N nonadecane Chemical compound CCCCCCCCCCCCCCCCCCC LQERIDTXQFOHKA-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 235000021313 oleic acid Nutrition 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- MUJIDPITZJWBSW-UHFFFAOYSA-N palladium(2+) Chemical compound [Pd+2] MUJIDPITZJWBSW-UHFFFAOYSA-N 0.000 description 2
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 2
- OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical compound OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 description 2
- 230000008659 phytopathology Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 159000000001 potassium salts Chemical class 0.000 description 2
- CPTJXGLQLVPIGP-UHFFFAOYSA-N precocene I Chemical compound C1=CC(C)(C)OC2=CC(OC)=CC=C21 CPTJXGLQLVPIGP-UHFFFAOYSA-N 0.000 description 2
- PTIDGSWTMLSGAH-UHFFFAOYSA-N precocene II Chemical compound O1C(C)(C)C=CC2=C1C=C(OC)C(OC)=C2 PTIDGSWTMLSGAH-UHFFFAOYSA-N 0.000 description 2
- CPAUHNHNGALXSY-UHFFFAOYSA-N propan-2-yl n-butylcarbamate Chemical compound CCCCNC(=O)OC(C)C CPAUHNHNGALXSY-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 2
- DHTJFQWHCVTNRY-OEMAIJDKSA-N pyrisoxazole Chemical compound C1([C@@]2(C)CC(ON2C)C=2C=CC(Cl)=CC=2)=CC=CN=C1 DHTJFQWHCVTNRY-OEMAIJDKSA-N 0.000 description 2
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 2
- WRPIRSINYZBGPK-UHFFFAOYSA-N quinoxyfen Chemical compound C1=CC(F)=CC=C1OC1=CC=NC2=CC(Cl)=CC(Cl)=C12 WRPIRSINYZBGPK-UHFFFAOYSA-N 0.000 description 2
- 238000012827 research and development Methods 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 229940080817 rotenone Drugs 0.000 description 2
- JUVIOZPCNVVQFO-UHFFFAOYSA-N rotenone Natural products O1C2=C3CC(C(C)=C)OC3=CC=C2C(=O)C2C1COC1=C2C=C(OC)C(OC)=C1 JUVIOZPCNVVQFO-UHFFFAOYSA-N 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000004071 soot Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 230000000707 stereoselective effect Effects 0.000 description 2
- 150000003432 sterols Chemical class 0.000 description 2
- 235000003702 sterols Nutrition 0.000 description 2
- QMGVPVSNSZLJIA-FVWCLLPLSA-N strychnine Chemical compound O([C@H]1CC(N([C@H]2[C@H]1[C@H]1C3)C=4C5=CC=CC=4)=O)CC=C1CN1[C@@H]3[C@]25CC1 QMGVPVSNSZLJIA-FVWCLLPLSA-N 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- OHEFFKYYKJVVOX-UHFFFAOYSA-N sulcatol Chemical compound CC(O)CCC=C(C)C OHEFFKYYKJVVOX-UHFFFAOYSA-N 0.000 description 2
- NMGNJWORLGLLHQ-UHFFFAOYSA-M sulcofuron-sodium Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 NMGNJWORLGLLHQ-UHFFFAOYSA-M 0.000 description 2
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 2
- 239000000375 suspending agent Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 235000013616 tea Nutrition 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 125000004192 tetrahydrofuran-2-yl group Chemical group [H]C1([H])OC([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 2
- RSOBJVBYZCMJOS-CYBMUJFWSA-N tolprocarb Chemical compound FC(F)(F)COC(=O)N[C@@H](C(C)C)CNC(=O)C1=CC=C(C)C=C1 RSOBJVBYZCMJOS-CYBMUJFWSA-N 0.000 description 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 2
- DFFWZNDCNBOKDI-UHFFFAOYSA-N trinexapac Chemical compound O=C1CC(C(=O)O)CC(=O)C1=C(O)C1CC1 DFFWZNDCNBOKDI-UHFFFAOYSA-N 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 108700026215 vpr Genes Proteins 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- FQTLCLSUCSAZDY-UHFFFAOYSA-N (+) E(S) nerolidol Natural products CC(C)=CCCC(C)=CCCC(C)(O)C=C FQTLCLSUCSAZDY-UHFFFAOYSA-N 0.000 description 1
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 1
- XEEQGYMUWCZPDN-DOMZBBRYSA-N (-)-(11S,2'R)-erythro-mefloquine Chemical compound C([C@@H]1[C@@H](O)C=2C3=CC=CC(=C3N=C(C=2)C(F)(F)F)C(F)(F)F)CCCN1 XEEQGYMUWCZPDN-DOMZBBRYSA-N 0.000 description 1
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
- CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 description 1
- YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 description 1
- AEPMMTRERWOSHG-HULFFUFUSA-N (1E,3E)-dodeca-1,3-dien-1-ol Chemical compound CCCCCCCC\C=C\C=C\O AEPMMTRERWOSHG-HULFFUFUSA-N 0.000 description 1
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 1
- WRGKWWRFSUGDPX-HUUCEWRRSA-N (1R,2R)-1-(4-chlorophenyl)-2-(1,2,4-triazol-1-yl)cycloheptan-1-ol Chemical compound N1([C@@H]2CCCCC[C@@]2(O)C=2C=CC(Cl)=CC=2)C=NC=N1 WRGKWWRFSUGDPX-HUUCEWRRSA-N 0.000 description 1
- GXEKYRXVRROBEV-FBXFSONDSA-N (1r,2s,3r,4s)-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid Chemical compound C1C[C@@H]2[C@@H](C(O)=O)[C@@H](C(=O)O)[C@H]1O2 GXEKYRXVRROBEV-FBXFSONDSA-N 0.000 description 1
- LOGJGKGBKZOEKZ-ZDCRXTMVSA-N (1r,3r,5s,6s)-5-ethyl-1,3,6-trimethyl-4,8-dioxabicyclo[3.2.1]octane Chemical compound O1[C@]2(C)C[C@H](C)[C@@]1(CC)O[C@H](C)C2 LOGJGKGBKZOEKZ-ZDCRXTMVSA-N 0.000 description 1
- AZWKCIZRVUVZPX-JGVFFNPUSA-N (1s,5r)-1,5-dimethyl-6,8-dioxabicyclo[3.2.1]octane Chemical compound C1CC[C@]2(C)OC[C@@]1(C)O2 AZWKCIZRVUVZPX-JGVFFNPUSA-N 0.000 description 1
- MKNJWAXSYGAMGJ-UHFFFAOYSA-N (2,3,4,5,6-pentachlorophenyl) dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl MKNJWAXSYGAMGJ-UHFFFAOYSA-N 0.000 description 1
- AGMMRUPNXPWLGF-AATRIKPKSA-N (2,3,5,6-tetrafluoro-4-methylphenyl)methyl 2,2-dimethyl-3-[(e)-prop-1-enyl]cyclopropane-1-carboxylate Chemical compound CC1(C)C(/C=C/C)C1C(=O)OCC1=C(F)C(F)=C(C)C(F)=C1F AGMMRUPNXPWLGF-AATRIKPKSA-N 0.000 description 1
- YHVJMJFNSRLYIC-WEVVVXLNSA-N (2,6-dinitro-4-octan-2-ylphenyl) (e)-but-2-enoate Chemical compound CCCCCCC(C)C1=CC([N+]([O-])=O)=C(OC(=O)\C=C\C)C([N+]([O-])=O)=C1 YHVJMJFNSRLYIC-WEVVVXLNSA-N 0.000 description 1
- CRDAMVZIKSXKFV-FBXUGWQNSA-N (2-cis,6-cis)-farnesol Chemical compound CC(C)=CCC\C(C)=C/CC\C(C)=C/CO CRDAMVZIKSXKFV-FBXUGWQNSA-N 0.000 description 1
- YMTQHWMPGDSBOD-UHFFFAOYSA-N (2-tert-butylpyrimidin-5-yl)oxy-diethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(=S)(OCC)OC1=CN=C(C(C)(C)C)N=C1 YMTQHWMPGDSBOD-UHFFFAOYSA-N 0.000 description 1
- 239000000260 (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol Substances 0.000 description 1
- GDPHPXYFLPDZGH-XBTMSFKCSA-N (2s)-2-[[(2s)-2-[[(2s)-2-[[2-[[(2r)-2-[[(2s)-2-amino-3-(4-hydroxyphenyl)propanoyl]amino]propanoyl]amino]acetyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid Chemical compound C([C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O)NC(=O)CNC(=O)[C@@H](C)NC(=O)[C@@H](N)CC=1C=CC(O)=CC=1)C1=CC=CC=C1 GDPHPXYFLPDZGH-XBTMSFKCSA-N 0.000 description 1
- ZCMOTOWEBLMCEO-UHFFFAOYSA-N (3-chloro-7-methylpyrazolo[1,5-a]pyrimidin-2-yl)oxy-diethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CC1=CC=NC2=C(Cl)C(OP(=S)(OCC)OCC)=NN21 ZCMOTOWEBLMCEO-UHFFFAOYSA-N 0.000 description 1
- IWNVUWRZPZAPAB-UHFFFAOYSA-N (4,4-dichloro-2-ethylsulfinylbut-3-enyl) methyl hydrogen phosphate Chemical compound CCS(=O)C(COP(=O)(O)OC)C=C(Cl)Cl IWNVUWRZPZAPAB-UHFFFAOYSA-N 0.000 description 1
- OZJCQBUSEOVJOW-UHFFFAOYSA-N (4-ethylsulfanylphenyl) n-methylcarbamate Chemical compound CCSC1=CC=C(OC(=O)NC)C=C1 OZJCQBUSEOVJOW-UHFFFAOYSA-N 0.000 description 1
- KEZAYQGUTKCBLO-UHFFFAOYSA-N (5,7-dichloro-1,3-benzoxazol-2-yl)methylsulfanyl-diethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound ClC1=CC(Cl)=C2OC(CSP(=S)(OCC)OCC)=NC2=C1 KEZAYQGUTKCBLO-UHFFFAOYSA-N 0.000 description 1
- VEMKTZHHVJILDY-PMACEKPBSA-N (5-benzylfuran-3-yl)methyl (1r,3s)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-PMACEKPBSA-N 0.000 description 1
- VEMKTZHHVJILDY-WOJBJXKFSA-N (5-benzylfuran-3-yl)methyl (1s,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-WOJBJXKFSA-N 0.000 description 1
- QTGIYXFCSKXKMO-XPSMFNQNSA-N (5r)-5-[(z)-dec-1-enyl]oxolan-2-one Chemical compound CCCCCCCC\C=C/[C@H]1CCC(=O)O1 QTGIYXFCSKXKMO-XPSMFNQNSA-N 0.000 description 1
- HMUURGZLCNRROC-JWPKELMXSA-N (6E,12Z)-hexadeca-6,12-dienoic acid Chemical compound CCC\C=C/CCCC\C=C\CCCCC(O)=O HMUURGZLCNRROC-JWPKELMXSA-N 0.000 description 1
- ALWJDQAPPAITSW-DNVGVPOPSA-N (9E,11Z)-tetradeca-9,11-dienoic acid Chemical compound CC\C=C/C=C/CCCCCCCC(O)=O ALWJDQAPPAITSW-DNVGVPOPSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- GSAAJQNJNPBBSX-UHFFFAOYSA-N (E)-form-9-Tetradecen-1-ol Natural products CCCCC=CCCCCCCCCO GSAAJQNJNPBBSX-UHFFFAOYSA-N 0.000 description 1
- TVYLLZQTGLZFBW-ZBFHGGJFSA-N (R,R)-tramadol Chemical compound COC1=CC=CC([C@]2(O)[C@H](CCCC2)CN(C)C)=C1 TVYLLZQTGLZFBW-ZBFHGGJFSA-N 0.000 description 1
- DARPYRSDRJYGIF-PTNGSMBKSA-N (Z)-3-ethoxy-2-naphthalen-2-ylsulfonylprop-2-enenitrile Chemical compound C1=CC=CC2=CC(S(=O)(=O)C(\C#N)=C/OCC)=CC=C21 DARPYRSDRJYGIF-PTNGSMBKSA-N 0.000 description 1
- PCKNFPQPGUWFHO-SXBRIOAWSA-N (Z)-flucycloxuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC(C=C1)=CC=C1CO\N=C(C=1C=CC(Cl)=CC=1)\C1CC1 PCKNFPQPGUWFHO-SXBRIOAWSA-N 0.000 description 1
- AMTITFMUKRZZEE-WAYWQWQTSA-N (Z)-hexadec-11-enal Chemical compound CCCC\C=C/CCCCCCCCCC=O AMTITFMUKRZZEE-WAYWQWQTSA-N 0.000 description 1
- JGMYDQCXGIMHLL-WAYWQWQTSA-N (Z)-hexadec-11-enoic acid Chemical compound CCCC\C=C/CCCCCCCCCC(O)=O JGMYDQCXGIMHLL-WAYWQWQTSA-N 0.000 description 1
- AQYQTFNATIWMRS-ARJAWSKDSA-N (Z)-octadec-15-en-13-ynoic acid Chemical compound CC\C=C/C#CCCCCCCCCCCCC(O)=O AQYQTFNATIWMRS-ARJAWSKDSA-N 0.000 description 1
- CKPCAYZTYMHQEX-NBVRZTHBSA-N (e)-1-(2,4-dichlorophenyl)-n-methoxy-2-pyridin-3-ylethanimine Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=N/OC)/CC1=CC=CN=C1 CKPCAYZTYMHQEX-NBVRZTHBSA-N 0.000 description 1
- AHUWMUAVZFJTOC-HNQUOIGGSA-N (e)-3-bromo-1-chloroprop-1-ene Chemical compound Cl\C=C\CBr AHUWMUAVZFJTOC-HNQUOIGGSA-N 0.000 description 1
- RQAFKZOPSRTJDU-SNAWJCMRSA-N (e)-6-methylhept-2-en-4-ol Chemical compound C\C=C\C(O)CC(C)C RQAFKZOPSRTJDU-SNAWJCMRSA-N 0.000 description 1
- QQVNWNVUGXNUJN-BENRWUELSA-N (e)-n-dimethoxyphosphinothioyloxybenzenecarboximidoyl cyanide Chemical compound COP(=S)(OC)O\N=C(\C#N)C1=CC=CC=C1 QQVNWNVUGXNUJN-BENRWUELSA-N 0.000 description 1
- IGOWHGRNPLFNDJ-ZPHPHTNESA-N (z)-9-tricosene Chemical compound CCCCCCCCCCCCC\C=C/CCCCCCCC IGOWHGRNPLFNDJ-ZPHPHTNESA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- APQIUTYORBAGEZ-UHFFFAOYSA-N 1,1-dibromoethane Chemical compound CC(Br)Br APQIUTYORBAGEZ-UHFFFAOYSA-N 0.000 description 1
- 125000001766 1,2,4-oxadiazol-3-yl group Chemical group [H]C1=NC(*)=NO1 0.000 description 1
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 description 1
- WBEJYOJJBDISQU-UHFFFAOYSA-N 1,2-Dibromo-3-chloropropane Chemical compound ClCC(Br)CBr WBEJYOJJBDISQU-UHFFFAOYSA-N 0.000 description 1
- 229940100682 1,2-dibromo-3-chloropropane Drugs 0.000 description 1
- KNKRKFALVUDBJE-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl KNKRKFALVUDBJE-UHFFFAOYSA-N 0.000 description 1
- JXBLYSQTCABEMR-UHFFFAOYSA-N 1,3-dihydrobenzimidazol-2-ylidene(methoxycarbonyl)azanium;chloride Chemical compound [Cl-].C1=CC=C2NC(=[NH+]C(=O)OC)NC2=C1 JXBLYSQTCABEMR-UHFFFAOYSA-N 0.000 description 1
- FXVNBZGTAWLLNE-UHFFFAOYSA-N 1,3-thiazole;zinc Chemical compound [Zn].C1=CSC=N1 FXVNBZGTAWLLNE-UHFFFAOYSA-N 0.000 description 1
- DSNHSQKRULAAEI-UHFFFAOYSA-N 1,4-Diethylbenzene Chemical compound CCC1=CC=C(CC)C=C1 DSNHSQKRULAAEI-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- HKELWJONQIFBPO-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1,2,4-triazole-3-carboxylic acid Chemical compound N1=C(C(=O)O)N=C(C(Cl)(Cl)Cl)N1C1=CC=C(Cl)C=C1Cl HKELWJONQIFBPO-UHFFFAOYSA-N 0.000 description 1
- ARGVNMTZBKWHEG-UHFFFAOYSA-N 1-(4,5-dimethylbenzimidazol-1-yl)-4,4-difluoro-3,3-dimethylisoquinoline Chemical compound CC1=C(C)C2=C(C=C1)N(C=N2)C1=NC(C)(C)C(F)(F)C2=C1C=CC=C2 ARGVNMTZBKWHEG-UHFFFAOYSA-N 0.000 description 1
- IHGSAQHSAGRWNI-UHFFFAOYSA-N 1-(4-bromophenyl)-2,2,2-trifluoroethanone Chemical compound FC(F)(F)C(=O)C1=CC=C(Br)C=C1 IHGSAQHSAGRWNI-UHFFFAOYSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical class CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- ULCWZQJLFZEXCS-UHFFFAOYSA-N 1-[[2-(2,4-dichlorophenyl)-5-(2,2,2-trifluoroethoxy)oxolan-2-yl]methyl]-1,2,4-triazole Chemical compound O1C(OCC(F)(F)F)CCC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 ULCWZQJLFZEXCS-UHFFFAOYSA-N 0.000 description 1
- RXZRAOONKFIKQQ-UHFFFAOYSA-N 1-[amino(aziridin-1-yl)phosphinothioyl]aziridine Chemical compound C1CN1P(=S)(N)N1CC1 RXZRAOONKFIKQQ-UHFFFAOYSA-N 0.000 description 1
- COVKSLBAQCJQMS-UHFFFAOYSA-N 1-chloro-4-[(4-chlorophenoxy)methoxy]benzene Chemical compound C1=CC(Cl)=CC=C1OCOC1=CC=C(Cl)C=C1 COVKSLBAQCJQMS-UHFFFAOYSA-N 0.000 description 1
- OTKWDNCXANVGKB-UHFFFAOYSA-N 1-n,1-n-diethyl-4-n-(7-fluoroquinolin-4-yl)pentane-1,4-diamine Chemical compound FC1=CC=C2C(NC(C)CCCN(CC)CC)=CC=NC2=C1 OTKWDNCXANVGKB-UHFFFAOYSA-N 0.000 description 1
- PRPINYUDVPFIRX-UHFFFAOYSA-N 1-naphthaleneacetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CC=CC2=C1 PRPINYUDVPFIRX-UHFFFAOYSA-N 0.000 description 1
- PNXGNYJXJBKFRG-UHFFFAOYSA-N 1-pent-4-ynoxy-4-phenoxybenzene Chemical compound C1=CC(OCCCC#C)=CC=C1OC1=CC=CC=C1 PNXGNYJXJBKFRG-UHFFFAOYSA-N 0.000 description 1
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- WZXXZHONLFRKGG-UHFFFAOYSA-N 2,3,4,5-tetrachlorothiophene Chemical compound ClC=1SC(Cl)=C(Cl)C=1Cl WZXXZHONLFRKGG-UHFFFAOYSA-N 0.000 description 1
- SVPKNMBRVBMTLB-UHFFFAOYSA-N 2,3-dichloronaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(Cl)=C(Cl)C(=O)C2=C1 SVPKNMBRVBMTLB-UHFFFAOYSA-N 0.000 description 1
- HXKWSTRRCHTUEC-UHFFFAOYSA-N 2,4-Dichlorophenoxyaceticacid Chemical compound OC(=O)C(Cl)OC1=CC=C(Cl)C=C1 HXKWSTRRCHTUEC-UHFFFAOYSA-N 0.000 description 1
- ZGPVUVBRTCPAPZ-UHFFFAOYSA-N 2,4-dichloro-1-[ethoxy(propylsulfanyl)phosphoryl]oxybenzene Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Cl)C=C1Cl ZGPVUVBRTCPAPZ-UHFFFAOYSA-N 0.000 description 1
- CCBICDLNWJRFPO-UHFFFAOYSA-N 2,6-dichloroindophenol Chemical compound C1=CC(O)=CC=C1N=C1C=C(Cl)C(=O)C(Cl)=C1 CCBICDLNWJRFPO-UHFFFAOYSA-N 0.000 description 1
- JTHMHWAHAKLCKT-UHFFFAOYSA-N 2,6-difluoro-n-[[4-(trifluoromethyl)phenyl]carbamoyl]benzamide Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(C(F)(F)F)C=C1 JTHMHWAHAKLCKT-UHFFFAOYSA-N 0.000 description 1
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
- DNBMPXLFKQCOBV-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OCCOCCOCC)=NC2=C1 DNBMPXLFKQCOBV-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- PVWMAOPFDINGAY-UHFFFAOYSA-N 2-(3-methylbutanoyl)indene-1,3-dione Chemical compound C1=CC=C2C(=O)C(C(=O)CC(C)C)C(=O)C2=C1 PVWMAOPFDINGAY-UHFFFAOYSA-N 0.000 description 1
- UZXFXOSXXYLVMI-UHFFFAOYSA-N 2-(4-chloro-3,5-dimethylphenoxy)ethanol Chemical compound CC1=CC(OCCO)=CC(C)=C1Cl UZXFXOSXXYLVMI-UHFFFAOYSA-N 0.000 description 1
- KXPXKNBDCUOENF-UHFFFAOYSA-N 2-(Octylthio)ethanol Chemical compound CCCCCCCCSCCO KXPXKNBDCUOENF-UHFFFAOYSA-N 0.000 description 1
- CDWPZHIPIACZRT-UHFFFAOYSA-N 2-(difluoromethyl)-N-(3-ethyl-1,1-dimethyl-2,3-dihydroinden-4-yl)pyridine-3-carboxamide Chemical compound CCC1CC(C)(C)C2=CC=CC(NC(=O)C3=CC=CN=C3C(F)F)=C12 CDWPZHIPIACZRT-UHFFFAOYSA-N 0.000 description 1
- CDWPZHIPIACZRT-GFCCVEGCSA-N 2-(difluoromethyl)-N-[(3R)-3-ethyl-1,1-dimethyl-2,3-dihydroinden-4-yl]pyridine-3-carboxamide Chemical compound FC(C1=NC=CC=C1C(=O)NC1=C2[C@@H](CC(C2=CC=C1)(C)C)CC)F CDWPZHIPIACZRT-GFCCVEGCSA-N 0.000 description 1
- CDWPZHIPIACZRT-LBPRGKRZSA-N 2-(difluoromethyl)-N-[(3S)-3-ethyl-1,1-dimethyl-2,3-dihydroinden-4-yl]pyridine-3-carboxamide Chemical compound FC(C1=NC=CC=C1C(=O)NC1=C2[C@H](CC(C2=CC=C1)(C)C)CC)F CDWPZHIPIACZRT-LBPRGKRZSA-N 0.000 description 1
- KAQJMEHRXVENSF-UHFFFAOYSA-N 2-(trichloromethyl)pyridine Chemical compound ClC(Cl)(Cl)C1=CC=CC=N1 KAQJMEHRXVENSF-UHFFFAOYSA-N 0.000 description 1
- IUVCFHHAEHNCFT-INIZCTEOSA-N 2-[(1s)-1-[4-amino-3-(3-fluoro-4-propan-2-yloxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]ethyl]-6-fluoro-3-(3-fluorophenyl)chromen-4-one Chemical compound C1=C(F)C(OC(C)C)=CC=C1C(C1=C(N)N=CN=C11)=NN1[C@@H](C)C1=C(C=2C=C(F)C=CC=2)C(=O)C2=CC(F)=CC=C2O1 IUVCFHHAEHNCFT-INIZCTEOSA-N 0.000 description 1
- IFEGQFVZKLLETD-UHFFFAOYSA-N 2-[(iodoamino)methyl]phenol Chemical compound C1=CC(O)=C(CNI)C=C1 IFEGQFVZKLLETD-UHFFFAOYSA-N 0.000 description 1
- BOTNFCTYKJBUMU-UHFFFAOYSA-N 2-[4-(2-methylpropyl)piperazin-4-ium-1-yl]-2-oxoacetate Chemical compound CC(C)C[NH+]1CCN(C(=O)C([O-])=O)CC1 BOTNFCTYKJBUMU-UHFFFAOYSA-N 0.000 description 1
- YVSGEOVSUKBTKQ-SUMWQHHRSA-N 2-[[(1R,5S)-5-[(4-fluorophenyl)methyl]-1-hydroxy-2,2-dimethylcyclopentyl]methyl]-1H-1,2,4-triazole-3-thione Chemical compound FC1=CC=C(C=C1)C[C@@H]1CCC([C@@]1(O)CN1N=CNC1=S)(C)C YVSGEOVSUKBTKQ-SUMWQHHRSA-N 0.000 description 1
- VNSVUCYVBBYLQR-UHFFFAOYSA-N 2-[[3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl]-1h-1,2,4-triazole-3-thione Chemical compound FC1=CC(F)=CC=C1C1(CN2C(NC=N2)=S)C(C=2C(=CC=CC=2)Cl)O1 VNSVUCYVBBYLQR-UHFFFAOYSA-N 0.000 description 1
- ULNWEXDKQHEUSK-UHFFFAOYSA-N 2-[ethoxy-(propan-2-ylamino)phosphoryl]sulfanyl-n-methyl-n-phenylacetamide Chemical compound CCOP(=O)(NC(C)C)SCC(=O)N(C)C1=CC=CC=C1 ULNWEXDKQHEUSK-UHFFFAOYSA-N 0.000 description 1
- PVTHJAPFENJVNC-UHFFFAOYSA-N 2-amino-2-[5-amino-2-methyl-6-(2,3,4,5,6-pentahydroxycyclohexyl)oxyoxan-3-yl]iminoacetic acid Chemical compound NC1CC(N=C(N)C(O)=O)C(C)OC1OC1C(O)C(O)C(O)C(O)C1O PVTHJAPFENJVNC-UHFFFAOYSA-N 0.000 description 1
- JUIKUQOUMZUFQT-UHFFFAOYSA-N 2-bromoacetamide Chemical compound NC(=O)CBr JUIKUQOUMZUFQT-UHFFFAOYSA-N 0.000 description 1
- HBZHNVUMFPGVHW-UHFFFAOYSA-N 2-chloro-1h-indole Chemical compound C1=CC=C2NC(Cl)=CC2=C1 HBZHNVUMFPGVHW-UHFFFAOYSA-N 0.000 description 1
- YHKBGVDUSSWOAB-UHFFFAOYSA-N 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoic acid Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(CC(Cl)C(O)=O)=C(Cl)C=C1F YHKBGVDUSSWOAB-UHFFFAOYSA-N 0.000 description 1
- DKMDOBOUUAGJNY-UHFFFAOYSA-N 2-chloroethenyl diethyl phosphate Chemical compound CCOP(=O)(OCC)OC=CCl DKMDOBOUUAGJNY-UHFFFAOYSA-N 0.000 description 1
- KKZUMAMOMRDVKA-UHFFFAOYSA-N 2-chloropropane Chemical group [CH2]C(C)Cl KKZUMAMOMRDVKA-UHFFFAOYSA-N 0.000 description 1
- QTAXOYGTNVSCHI-UHFFFAOYSA-N 2-ethyl-1-methoxypiperidine Chemical compound CCC1CCCCN1OC QTAXOYGTNVSCHI-UHFFFAOYSA-N 0.000 description 1
- FVTWJXMFYOXOKK-UHFFFAOYSA-N 2-fluoroacetamide Chemical compound NC(=O)CF FVTWJXMFYOXOKK-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- JNODDICFTDYODH-UHFFFAOYSA-N 2-hydroxytetrahydrofuran Chemical compound OC1CCCO1 JNODDICFTDYODH-UHFFFAOYSA-N 0.000 description 1
- MDURQPNBPHBIFN-UHFFFAOYSA-N 2-pentoxyphenol Chemical compound CCCCCOC1=CC=CC=C1O MDURQPNBPHBIFN-UHFFFAOYSA-N 0.000 description 1
- TWBPWBPGNQWFSJ-UHFFFAOYSA-N 2-phenylaniline Chemical group NC1=CC=CC=C1C1=CC=CC=C1 TWBPWBPGNQWFSJ-UHFFFAOYSA-N 0.000 description 1
- DXTLBEQSVNRVKT-UHFFFAOYSA-N 2-thiocyanatoethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCSC#N DXTLBEQSVNRVKT-UHFFFAOYSA-N 0.000 description 1
- NKDFYOWSKOHCCO-YPVLXUMRSA-N 20-hydroxyecdysone Chemical compound C1[C@@H](O)[C@@H](O)C[C@]2(C)[C@@H](CC[C@@]3([C@@H]([C@@](C)(O)[C@H](O)CCC(C)(O)C)CC[C@]33O)C)C3=CC(=O)[C@@H]21 NKDFYOWSKOHCCO-YPVLXUMRSA-N 0.000 description 1
- HXWZQRICWSADMH-SEHXZECUSA-N 20-hydroxyecdysone Natural products CC(C)(C)CC[C@@H](O)[C@@](C)(O)[C@H]1CC[C@@]2(O)C3=CC(=O)[C@@H]4C[C@@H](O)[C@@H](O)C[C@]4(C)[C@H]3CC[C@]12C HXWZQRICWSADMH-SEHXZECUSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- AUQAUAIUNJIIEP-UHFFFAOYSA-N 3,4,5-trimethylphenyl methylcarbamate Chemical compound CNC(=O)OC1=CC(C)=C(C)C(C)=C1 AUQAUAIUNJIIEP-UHFFFAOYSA-N 0.000 description 1
- JCUQWSIALJCIEE-UHFFFAOYSA-N 3,4-dichlorothiolane 1,1-dioxide Chemical compound ClC1CS(=O)(=O)CC1Cl JCUQWSIALJCIEE-UHFFFAOYSA-N 0.000 description 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 1
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 1
- SWBHWUYHHJCADA-UHFFFAOYSA-N 3-(2-chlorophenyl)-6-(2,6-difluorophenyl)-1,2,4,5-tetrazine Chemical compound FC1=CC=CC(F)=C1C1=NN=C(C=2C(=CC=CC=2)Cl)N=N1 SWBHWUYHHJCADA-UHFFFAOYSA-N 0.000 description 1
- HLBOAQSKBNNHMW-UHFFFAOYSA-N 3-(3-methoxyphenyl)pyridine Chemical compound COC1=CC=CC(C=2C=NC=CC=2)=C1 HLBOAQSKBNNHMW-UHFFFAOYSA-N 0.000 description 1
- PSPHGOSKTQOWBU-UHFFFAOYSA-N 3-(4,4-difluoro-3,3-dimethylisoquinolin-1-yl)-1h-quinolin-2-one Chemical compound C1=CC=C2NC(=O)C(C3=NC(C(C4=CC=CC=C43)(F)F)(C)C)=CC2=C1 PSPHGOSKTQOWBU-UHFFFAOYSA-N 0.000 description 1
- IBWJXVVIEGGYGU-UHFFFAOYSA-N 3-(4-chlorophenyl)-5-methyl-2-sulfanylidene-1,3-thiazolidin-4-one Chemical compound O=C1C(C)SC(=S)N1C1=CC=C(Cl)C=C1 IBWJXVVIEGGYGU-UHFFFAOYSA-N 0.000 description 1
- OMSQGGMSQNHEMG-UHFFFAOYSA-N 3-chloro-6-methyl-5-phenyl-4-(2,4,6-trifluorophenyl)pyridazine Chemical compound CC1=NN=C(Cl)C(C=2C(=CC(F)=CC=2F)F)=C1C1=CC=CC=C1 OMSQGGMSQNHEMG-UHFFFAOYSA-N 0.000 description 1
- SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 description 1
- PMYDPQQPEAYXKD-UHFFFAOYSA-N 3-hydroxy-n-naphthalen-2-ylnaphthalene-2-carboxamide Chemical compound C1=CC=CC2=CC(NC(=O)C3=CC4=CC=CC=C4C=C3O)=CC=C21 PMYDPQQPEAYXKD-UHFFFAOYSA-N 0.000 description 1
- VVJPJXKHBZNADP-QQIRETTESA-N 3E,13E-Octadecadienyl acetate Chemical compound CCCC\C=C\CCCCCCCC\C=C\CCOC(C)=O VVJPJXKHBZNADP-QQIRETTESA-N 0.000 description 1
- PKTIFYGCWCQRSX-UHFFFAOYSA-N 4,6-diamino-2-(cyclopropylamino)pyrimidine-5-carbonitrile Chemical compound NC1=C(C#N)C(N)=NC(NC2CC2)=N1 PKTIFYGCWCQRSX-UHFFFAOYSA-N 0.000 description 1
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 1
- SAXRAUVIWMPORK-UHFFFAOYSA-N 4-(2,6-difluorophenyl)-6-methyl-5-phenylpyridazine-3-carbonitrile Chemical compound C=1C=CC=CC=1C=1C(C)=NN=C(C#N)C=1C1=C(F)C=CC=C1F SAXRAUVIWMPORK-UHFFFAOYSA-N 0.000 description 1
- LBGMYUQCXJJLIR-UHFFFAOYSA-N 4-(2-bromo-4-fluorophenyl)-n-(2-chloro-6-fluorophenyl)-2,5-dimethylpyrazol-3-amine Chemical compound C=1C=C(F)C=C(Br)C=1C=1C(C)=NN(C)C=1NC1=C(F)C=CC=C1Cl LBGMYUQCXJJLIR-UHFFFAOYSA-N 0.000 description 1
- AIZZVQVZTSSOHN-UHFFFAOYSA-N 4-(2-chloro-6-fluorophenyl)-2,5-dimethylpyrazol-3-amine Chemical compound CC1=NN(C)C(N)=C1C1=C(F)C=CC=C1Cl AIZZVQVZTSSOHN-UHFFFAOYSA-N 0.000 description 1
- HDNVYHWHCVTDIV-UHFFFAOYSA-N 4-[(2-amino-3-hydroxy-2-methylpropanoyl)amino]-n-[1-[5-[5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]-2-oxopyrimidin-4-yl]benzamide Chemical compound CC1OC(N2C(N=C(NC(=O)C=3C=CC(NC(=O)C(C)(N)CO)=CC=3)C=C2)=O)CCC1OC1OC(C)C(N(C)C)C(O)C1O HDNVYHWHCVTDIV-UHFFFAOYSA-N 0.000 description 1
- TZFNCHJVUIEWRA-UHFFFAOYSA-N 4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide Chemical compound NC(=O)C1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F TZFNCHJVUIEWRA-UHFFFAOYSA-N 0.000 description 1
- JTCSEWBIRWUSAV-UHFFFAOYSA-N 4-[6-[2-(2,4-difluorophenyl)-1,1-difluoro-2-hydroxy-3-(1,2,4-triazol-1-yl)propyl]pyridin-3-yl]oxybenzonitrile Chemical compound FC1=C(C=CC(=C1)F)C(C(F)(F)C1=CC=C(C=N1)OC1=CC=C(C#N)C=C1)(CN1N=CN=C1)O JTCSEWBIRWUSAV-UHFFFAOYSA-N 0.000 description 1
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 description 1
- QKNNWDFHKRIYJH-UHFFFAOYSA-N 4-bromo-3-fluorobenzoyl chloride Chemical compound FC1=CC(C(Cl)=O)=CC=C1Br QKNNWDFHKRIYJH-UHFFFAOYSA-N 0.000 description 1
- GICUQIXVWFUPOQ-UHFFFAOYSA-N 4-chloro-2-(2-chloro-2-methylpropyl)-5-[(6-iodopyridin-3-yl)methoxy]pyridazin-3-one Chemical compound O=C1N(CC(C)(Cl)C)N=CC(OCC=2C=NC(I)=CC=2)=C1Cl GICUQIXVWFUPOQ-UHFFFAOYSA-N 0.000 description 1
- DGHSHWFCCLCSMN-UHFFFAOYSA-N 4-iodo-3h-quinazolin-2-one Chemical compound C1=CC=C2C(I)=NC(=O)NC2=C1 DGHSHWFCCLCSMN-UHFFFAOYSA-N 0.000 description 1
- KVARTGUGROJGNK-UHFFFAOYSA-N 4-nitrobutyl nitrate Chemical compound [N+](=O)(OCCCC[N+](=O)[O-])[O-] KVARTGUGROJGNK-UHFFFAOYSA-N 0.000 description 1
- JBVNWTXRFKZNBQ-UHFFFAOYSA-N 5-(1,3-benzodioxol-5-yl)-3-hexylcyclohex-2-en-1-one Chemical compound C1C(CCCCCC)=CC(=O)CC1C1=CC=C(OCO2)C2=C1 JBVNWTXRFKZNBQ-UHFFFAOYSA-N 0.000 description 1
- RSNWORHVUOZYLT-UHFFFAOYSA-N 5-[[(2-sulfanylidene-3h-1,3,4-thiadiazol-5-yl)amino]methylamino]-3h-1,3,4-thiadiazole-2-thione Chemical compound S1C(=S)NN=C1NCNC1=NNC(=S)S1 RSNWORHVUOZYLT-UHFFFAOYSA-N 0.000 description 1
- OONJCAWRVJDVBB-UHFFFAOYSA-N 5-bromo-2-methylphenol Chemical compound CC1=CC=C(Br)C=C1O OONJCAWRVJDVBB-UHFFFAOYSA-N 0.000 description 1
- QRXMUCSWCMTJGU-UHFFFAOYSA-N 5-bromo-4-chloro-3-indolyl phosphate Chemical compound C1=C(Br)C(Cl)=C2C(OP(O)(=O)O)=CNC2=C1 QRXMUCSWCMTJGU-UHFFFAOYSA-N 0.000 description 1
- SJDGOKGRYGWNTC-UHFFFAOYSA-N 5-isothiocyanato-2-methoxy-n,n,3-trimethylbenzamide Chemical compound COC1=C(C)C=C(N=C=S)C=C1C(=O)N(C)C SJDGOKGRYGWNTC-UHFFFAOYSA-N 0.000 description 1
- BBEBRBQWJLBJKN-UHFFFAOYSA-N 6-(3-methylbut-3-enyl)-7H-purin-2-amine Chemical compound C(CC(=C)C)C1=C2NC=NC2=NC(=N1)N BBEBRBQWJLBJKN-UHFFFAOYSA-N 0.000 description 1
- FLXHSKWGRNEFSP-UHFFFAOYSA-N 6-chloro-4,4-difluoro-3,3-dimethyl-1-(4-methylbenzimidazol-1-yl)isoquinoline Chemical compound CC1=CC=CC2=C1N=CN2C1=NC(C)(C)C(F)(F)C2=C1C=CC(Cl)=C2 FLXHSKWGRNEFSP-UHFFFAOYSA-N 0.000 description 1
- VSVKOUBCDZYAQY-UHFFFAOYSA-N 7-chloro-1,2-benzothiazole Chemical compound ClC1=CC=CC2=C1SN=C2 VSVKOUBCDZYAQY-UHFFFAOYSA-N 0.000 description 1
- MUZGQHWTRUVFLG-SREVYHEPSA-N 7Z-Dodecenyl acetate Chemical compound CCCC\C=C/CCCCCCOC(C)=O MUZGQHWTRUVFLG-SREVYHEPSA-N 0.000 description 1
- HVUBXNQWXJBVHB-SQFISAMPSA-N 7Z-Eicosen-11-one Chemical compound CCCCCCCCCC(=O)CC\C=C/CCCCCC HVUBXNQWXJBVHB-SQFISAMPSA-N 0.000 description 1
- AVHNDAZRNRAYTP-FPLPWBNLSA-N 7Z-Tetradecenal Chemical compound CCCCCC\C=C/CCCCCC=O AVHNDAZRNRAYTP-FPLPWBNLSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- GZSUIHUAFPHZSU-UHFFFAOYSA-N 9-ethyl-2,3-dihydro-1h-carbazol-4-one Chemical compound C12=CC=CC=C2N(CC)C2=C1C(=O)CCC2 GZSUIHUAFPHZSU-UHFFFAOYSA-N 0.000 description 1
- JVGXNGXFTFLIGB-UHFFFAOYSA-N 9-fluoro-2,2-dimethyl-5-quinolin-3-yl-3h-1,4-benzoxazepine Chemical compound C12=CC=CC(F)=C2OC(C)(C)CN=C1C1=CN=C(C=CC=C2)C2=C1 JVGXNGXFTFLIGB-UHFFFAOYSA-N 0.000 description 1
- GSAAJQNJNPBBSX-WAYWQWQTSA-N 9Z-Tetradecen-1-ol Chemical compound CCCC\C=C/CCCCCCCCO GSAAJQNJNPBBSX-WAYWQWQTSA-N 0.000 description 1
- 240000004507 Abelmoschus esculentus Species 0.000 description 1
- 206010063409 Acarodermatitis Diseases 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 241001019659 Acremonium <Plectosphaerellaceae> Species 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 244000251953 Agaricus brunnescens Species 0.000 description 1
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 1
- 244000198134 Agave sisalana Species 0.000 description 1
- 241000589155 Agrobacterium tumefaciens Species 0.000 description 1
- 241000743339 Agrostis Species 0.000 description 1
- 108700029992 Ala(2)-Arg(6)- enkephalin-Leu Proteins 0.000 description 1
- 241001103808 Albifimbria verrucaria Species 0.000 description 1
- 241000919507 Albugo candida Species 0.000 description 1
- 241001163841 Albugo ipomoeae-panduratae Species 0.000 description 1
- YRRKLBAKDXSTNC-WEVVVXLNSA-N Aldoxycarb Chemical compound CNC(=O)O\N=C\C(C)(C)S(C)(=O)=O YRRKLBAKDXSTNC-WEVVVXLNSA-N 0.000 description 1
- 241000234282 Allium Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- 235000008553 Allium fistulosum Nutrition 0.000 description 1
- 244000257727 Allium fistulosum Species 0.000 description 1
- 235000001270 Allium sibiricum Nutrition 0.000 description 1
- 244000016163 Allium sibiricum Species 0.000 description 1
- 241000406588 Amblyseius Species 0.000 description 1
- 241000187643 Amycolatopsis Species 0.000 description 1
- 244000144725 Amygdalus communis Species 0.000 description 1
- 244000144730 Amygdalus persica Species 0.000 description 1
- 241000208223 Anacardiaceae Species 0.000 description 1
- 241000584992 Anagrus Species 0.000 description 1
- 241000393993 Aphia Species 0.000 description 1
- 241001600408 Aphis gossypii Species 0.000 description 1
- 241001344109 Apiognomonia Species 0.000 description 1
- 101100477360 Arabidopsis thaliana IPSP gene Proteins 0.000 description 1
- 241000239223 Arachnida Species 0.000 description 1
- 241000002053 Arcopilus cupreus Species 0.000 description 1
- 240000005528 Arctium lappa Species 0.000 description 1
- 235000003130 Arctium lappa Nutrition 0.000 description 1
- 235000008078 Arctium minus Nutrition 0.000 description 1
- 241000216654 Armillaria Species 0.000 description 1
- 241000222195 Ascochyta Species 0.000 description 1
- 244000003416 Asparagus officinalis Species 0.000 description 1
- 235000005340 Asparagus officinalis Nutrition 0.000 description 1
- 240000006439 Aspergillus oryzae Species 0.000 description 1
- 235000002247 Aspergillus oryzae Nutrition 0.000 description 1
- QAOFKYGUSMPWNY-UHFFFAOYSA-N Athidathion Chemical compound CCOP(=S)(OCC)SCN1N=C(OC)SC1=O QAOFKYGUSMPWNY-UHFFFAOYSA-N 0.000 description 1
- 241000223651 Aureobasidium Species 0.000 description 1
- 241000321828 Aureobasidium lini Species 0.000 description 1
- 235000000832 Ayote Nutrition 0.000 description 1
- 101100497219 Bacillus thuringiensis subsp. kurstaki cry1Ac gene Proteins 0.000 description 1
- 241000606125 Bacteroides Species 0.000 description 1
- 241001490361 Bactrocera minax Species 0.000 description 1
- 241000223679 Beauveria Species 0.000 description 1
- 241000751139 Beauveria bassiana Species 0.000 description 1
- RRNIZKPFKNDSRS-UHFFFAOYSA-N Bensulide Chemical compound CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)C1=CC=CC=C1 RRNIZKPFKNDSRS-UHFFFAOYSA-N 0.000 description 1
- 239000005736 Benthiavalicarb Substances 0.000 description 1
- 235000016068 Berberis vulgaris Nutrition 0.000 description 1
- 241000335053 Beta vulgaris Species 0.000 description 1
- 239000005884 Beta-Cyfluthrin Substances 0.000 description 1
- 239000005874 Bifenthrin Substances 0.000 description 1
- RQOLZRKNRJWASP-UHFFFAOYSA-N Bis(1-aziridinyl)morpholinophosphine sulfide Chemical compound C1CN1P(N1CCOCC1)(=S)N1CC1 RQOLZRKNRJWASP-UHFFFAOYSA-N 0.000 description 1
- ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 1
- 241000335423 Blastomyces Species 0.000 description 1
- 241001480060 Blumeria Species 0.000 description 1
- 241001480061 Blumeria graminis Species 0.000 description 1
- 235000007689 Borago officinalis Nutrition 0.000 description 1
- 240000004355 Borago officinalis Species 0.000 description 1
- 241000499339 Botrytis allii Species 0.000 description 1
- 241000167854 Bourreria succulenta Species 0.000 description 1
- 241000743774 Brachypodium Species 0.000 description 1
- 235000011331 Brassica Nutrition 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 description 1
- 235000006008 Brassica napus var napus Nutrition 0.000 description 1
- 235000011299 Brassica oleracea var botrytis Nutrition 0.000 description 1
- 235000017647 Brassica oleracea var italica Nutrition 0.000 description 1
- 240000003259 Brassica oleracea var. botrytis Species 0.000 description 1
- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- 244000188595 Brassica sinapistrum Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 239000005966 Bromadiolone Substances 0.000 description 1
- OWNRRUFOJXFKCU-UHFFFAOYSA-N Bromadiolone Chemical compound C=1C=C(C=2C=CC(Br)=CC=2)C=CC=1C(O)CC(C=1C(OC2=CC=CC=C2C=1O)=O)C1=CC=CC=C1 OWNRRUFOJXFKCU-UHFFFAOYSA-N 0.000 description 1
- 239000005489 Bromoxynil Substances 0.000 description 1
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 1
- COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 description 1
- OKIJSNGRQAOIGZ-UHFFFAOYSA-N Butopyronoxyl Chemical group CCCCOC(=O)C1=CC(=O)CC(C)(C)O1 OKIJSNGRQAOIGZ-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- RURBWVIWYOXPLG-ATVHPVEESA-N C1(=CCCCC1)C=1C=CC(=C(O\C(\C(=O)OC)=C/OC)C=1)C Chemical compound C1(=CCCCC1)C=1C=CC(=C(O\C(\C(=O)OC)=C/OC)C=1)C RURBWVIWYOXPLG-ATVHPVEESA-N 0.000 description 1
- VUWBMXNMKRWSEI-UHFFFAOYSA-N C1(CCCCC1)P(C1=C(C=CC=C1)C1=C(C=C(C=C1C(C)C)C(C)C)C(C)C)C1CCCCC1.[Cl] Chemical group C1(CCCCC1)P(C1=C(C=CC=C1)C1=C(C=C(C=C1C(C)C)C(C)C)C(C)C)C1CCCCC1.[Cl] VUWBMXNMKRWSEI-UHFFFAOYSA-N 0.000 description 1
- DTOZPNHGPWULBM-HSZRJFAPSA-N C1=C(C2=NC=C(C(=O)N[C@](CC(C)C)(CC3=CC(F)=CC=C3)C)C=C2C=C1)F Chemical compound C1=C(C2=NC=C(C(=O)N[C@](CC(C)C)(CC3=CC(F)=CC=C3)C)C=C2C=C1)F DTOZPNHGPWULBM-HSZRJFAPSA-N 0.000 description 1
- NHDRPDNCAMXMGL-UHFFFAOYSA-N CC(C(=O)N)CCCCC(C)(C)C.CC(C(=O)N)CCCCC(C)(C)C Chemical compound CC(C(=O)N)CCCCC(C)(C)C.CC(C(=O)N)CCCCC(C)(C)C NHDRPDNCAMXMGL-UHFFFAOYSA-N 0.000 description 1
- LXWBCUNFHMWIJY-UHFFFAOYSA-N CC1(CC(N(O1)CC1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F)=O)C Chemical compound CC1(CC(N(O1)CC1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F)=O)C LXWBCUNFHMWIJY-UHFFFAOYSA-N 0.000 description 1
- JFLRKDZMHNBDQS-UCQUSYKYSA-N CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C Chemical compound CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C JFLRKDZMHNBDQS-UCQUSYKYSA-N 0.000 description 1
- YFIQXDGHFSNIHQ-UHFFFAOYSA-N CN[PH2]=S.N1CC1.N1CC1 Chemical compound CN[PH2]=S.N1CC1.N1CC1 YFIQXDGHFSNIHQ-UHFFFAOYSA-N 0.000 description 1
- LMZXCAKAGHEUDK-QFIPXVFZSA-N C[C@](CC(Cl)=C)(Cc1ccccc1)NC(=O)c1cnc2c(F)cccc2c1 Chemical compound C[C@](CC(Cl)=C)(Cc1ccccc1)NC(=O)c1cnc2c(F)cccc2c1 LMZXCAKAGHEUDK-QFIPXVFZSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- RMBBSOLAGVEUSI-UHFFFAOYSA-H Calcium arsenate Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-][As]([O-])([O-])=O.[O-][As]([O-])([O-])=O RMBBSOLAGVEUSI-UHFFFAOYSA-H 0.000 description 1
- 241001246270 Calophyllum Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 241000876848 Capnodium Species 0.000 description 1
- 235000002566 Capsicum Nutrition 0.000 description 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 1
- 235000009025 Carya illinoensis Nutrition 0.000 description 1
- 244000068645 Carya illinoensis Species 0.000 description 1
- 241000219503 Casuarina equisetifolia Species 0.000 description 1
- 241001123632 Cephaloascus Species 0.000 description 1
- 241001435629 Cephalosporium gramineum Species 0.000 description 1
- 241000255579 Ceratitis capitata Species 0.000 description 1
- DBUCFOVFALNEOO-HWBIYQLFSA-N Cevadine Chemical compound C1[C@@H](C)CC[C@H]2[C@](O)(C)[C@@]3(O)[C@@H](O)C[C@@]4(O)[C@@H]5CC[C@H]6[C@]7(C)CC[C@H](OC(=O)C(\C)=C/C)[C@@]6(O)O[C@@]75C[C@@]4(O)[C@@H]3CN21 DBUCFOVFALNEOO-HWBIYQLFSA-N 0.000 description 1
- 241000227752 Chaetoceros Species 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 1
- XWCDCDSDNJVCLO-UHFFFAOYSA-N Chlorofluoromethane Chemical compound FCCl XWCDCDSDNJVCLO-UHFFFAOYSA-N 0.000 description 1
- OUDYXRYNDPEKLK-XNTDXEJSSA-N Chloromebuform Chemical compound CCCCN(C)\C=N\C1=CC=C(Cl)C=C1C OUDYXRYNDPEKLK-XNTDXEJSSA-N 0.000 description 1
- 241001451061 Choanephora cucurbitarum Species 0.000 description 1
- 241000862992 Chondromyces Species 0.000 description 1
- 241000865175 Chrysomyxa Species 0.000 description 1
- 241001292007 Chrysopa Species 0.000 description 1
- 241000258934 Chrysoperla Species 0.000 description 1
- 241000206751 Chrysophyceae Species 0.000 description 1
- 241000123346 Chrysosporium Species 0.000 description 1
- 241000223782 Ciliophora Species 0.000 description 1
- BZSZIAPWBMBDHX-UHFFFAOYSA-N ClC1=C(C=CC(=C1)Cl)N1N=C(C=C1)OCC=C(/C(/C(=O)NC)=NOC)C Chemical compound ClC1=C(C=CC(=C1)Cl)N1N=C(C=C1)OCC=C(/C(/C(=O)NC)=NOC)C BZSZIAPWBMBDHX-UHFFFAOYSA-N 0.000 description 1
- 241001508811 Clavispora Species 0.000 description 1
- 239000005498 Clodinafop Substances 0.000 description 1
- DBPRUZCKPFOVDV-UHFFFAOYSA-N Clorprenaline hydrochloride Chemical compound O.Cl.CC(C)NCC(O)C1=CC=CC=C1Cl DBPRUZCKPFOVDV-UHFFFAOYSA-N 0.000 description 1
- 241000193403 Clostridium Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 241000222380 Coleosporium Species 0.000 description 1
- 241001466031 Colletotrichum gossypii Species 0.000 description 1
- 241001480517 Conidiobolus Species 0.000 description 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 1
- 239000005750 Copper hydroxide Substances 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 241001266001 Cordyceps confragosa Species 0.000 description 1
- 235000002787 Coriandrum sativum Nutrition 0.000 description 1
- 244000018436 Coriandrum sativum Species 0.000 description 1
- 241000723382 Corylus Species 0.000 description 1
- 235000001543 Corylus americana Nutrition 0.000 description 1
- 240000007582 Corylus avellana Species 0.000 description 1
- 241000186216 Corynebacterium Species 0.000 description 1
- 241001081178 Cryptocarya Species 0.000 description 1
- 241000550745 Cryptolaemus montrouzieri Species 0.000 description 1
- 241000223935 Cryptosporidium Species 0.000 description 1
- 241001137883 Cucumaria Species 0.000 description 1
- 241000219112 Cucumis Species 0.000 description 1
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
- 241000219122 Cucurbita Species 0.000 description 1
- 235000009854 Cucurbita moschata Nutrition 0.000 description 1
- 240000001980 Cucurbita pepo Species 0.000 description 1
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 description 1
- 241000219130 Cucurbita pepo subsp. pepo Species 0.000 description 1
- 235000003954 Cucurbita pepo var melopepo Nutrition 0.000 description 1
- UMIKWXDGXDJQJK-UHFFFAOYSA-N Cuelure Chemical compound CC(=O)CCC1=CC=C(OC(C)=O)C=C1 UMIKWXDGXDJQJK-UHFFFAOYSA-N 0.000 description 1
- 241000256113 Culicidae Species 0.000 description 1
- 244000301850 Cupressus sempervirens Species 0.000 description 1
- 241000223211 Curvularia lunata Species 0.000 description 1
- 241000371644 Curvularia ravenelii Species 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- 241000426256 Cyanotis Species 0.000 description 1
- 241001635274 Cydia pomonella Species 0.000 description 1
- 240000004784 Cymbopogon citratus Species 0.000 description 1
- 235000017897 Cymbopogon citratus Nutrition 0.000 description 1
- 244000052363 Cynodon dactylon Species 0.000 description 1
- 239000005758 Cyprodinil Substances 0.000 description 1
- 108010075028 Cytochromes b Proteins 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 241000596037 Dacnusa sibirica Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- PZIRJMYRYORVIT-UHFFFAOYSA-N Demeton-S-methylsulphon Chemical compound CCS(=O)(=O)CCSP(=O)(OC)OC PZIRJMYRYORVIT-UHFFFAOYSA-N 0.000 description 1
- 102100034289 Deoxynucleoside triphosphate triphosphohydrolase SAMHD1 Human genes 0.000 description 1
- XTJFFFGAUHQWII-UHFFFAOYSA-N Dibutyl adipate Chemical compound CCCCOC(=O)CCCCC(=O)OCCCC XTJFFFGAUHQWII-UHFFFAOYSA-N 0.000 description 1
- YUXIBTJKHLUKBD-UHFFFAOYSA-N Dibutyl succinate Chemical compound CCCCOC(=O)CCC(=O)OCCCC YUXIBTJKHLUKBD-UHFFFAOYSA-N 0.000 description 1
- 241001331021 Dicarpella Species 0.000 description 1
- LWLJUMBEZJHXHV-UHFFFAOYSA-N Dienochlor Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C1(Cl)C1(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LWLJUMBEZJHXHV-UHFFFAOYSA-N 0.000 description 1
- 239000005759 Diethofencarb Substances 0.000 description 1
- 239000005947 Dimethoate Substances 0.000 description 1
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 1
- 240000001008 Dimocarpus longan Species 0.000 description 1
- QJYHUJAGJUHXJN-UHFFFAOYSA-N Dinex Chemical compound C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(O)=C1C1CCCCC1 QJYHUJAGJUHXJN-UHFFFAOYSA-N 0.000 description 1
- 241000461780 Diplocarpon Species 0.000 description 1
- 241000935926 Diplodia Species 0.000 description 1
- 241001307140 Diplodia seriata Species 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 241000560922 Discula Species 0.000 description 1
- 239000005764 Dithianon Substances 0.000 description 1
- 239000005766 Dodine Substances 0.000 description 1
- 241000471401 Dothiorella Species 0.000 description 1
- 101100117236 Drosophila melanogaster speck gene Proteins 0.000 description 1
- 208000035220 Dyserythropoietic Congenital Anemia Diseases 0.000 description 1
- 229920005682 EO-PO block copolymer Polymers 0.000 description 1
- DCEFCUHVANGEOE-UHFFFAOYSA-N Ecdysterone Natural products CC(CC(C)(C)O)C(O)C(C)(O)C1CCC2(O)C3=CC(=O)C4CC(O)C(O)CC4(C)C3CCC12C DCEFCUHVANGEOE-UHFFFAOYSA-N 0.000 description 1
- 235000001950 Elaeis guineensis Nutrition 0.000 description 1
- 244000127993 Elaeis melanococca Species 0.000 description 1
- 241000901048 Elsinoe ampelina Species 0.000 description 1
- 241001454772 Encarsia formosa Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 241000283070 Equus zebra Species 0.000 description 1
- 241001465321 Eremothecium Species 0.000 description 1
- 241000588694 Erwinia amylovora Species 0.000 description 1
- 241000221785 Erysiphales Species 0.000 description 1
- 241000510928 Erysiphe necator Species 0.000 description 1
- 241000360593 Erythroides Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005961 Ethoprophos Substances 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- FGIWFCGDPUIBEZ-UHFFFAOYSA-N Etrimfos Chemical compound CCOC1=CC(OP(=S)(OC)OC)=NC(CC)=N1 FGIWFCGDPUIBEZ-UHFFFAOYSA-N 0.000 description 1
- 239000005770 Eugenol Substances 0.000 description 1
- 235000000235 Euphoria longan Nutrition 0.000 description 1
- 241001661371 Exobasidium vexans Species 0.000 description 1
- 241000223682 Exophiala Species 0.000 description 1
- 241000306559 Exserohilum Species 0.000 description 1
- DTOZPNHGPWULBM-QHCPKHFHSA-N FC=1C=CC=C2C=C(C=NC=12)C(=O)N[C@](CC(C)C)(C)CC1=CC(=CC=C1)F Chemical compound FC=1C=CC=C2C=C(C=NC=12)C(=O)N[C@](CC(C)C)(C)CC1=CC(=CC=C1)F DTOZPNHGPWULBM-QHCPKHFHSA-N 0.000 description 1
- 241001316058 Fabiana Species 0.000 description 1
- 239000005774 Fenamidone Substances 0.000 description 1
- 239000005958 Fenamiphos (aka phenamiphos) Substances 0.000 description 1
- 241000218218 Ficus <angiosperm> Species 0.000 description 1
- 239000005900 Flonicamid Substances 0.000 description 1
- 239000005901 Flubendiamide Substances 0.000 description 1
- 241001480539 Fomitopsis rosea Species 0.000 description 1
- 241000220223 Fragaria Species 0.000 description 1
- 235000016623 Fragaria vesca Nutrition 0.000 description 1
- 235000011363 Fragaria x ananassa Nutrition 0.000 description 1
- 239000005791 Fuberidazole Substances 0.000 description 1
- 241000879841 Fusarium oxysporum f. cubense Species 0.000 description 1
- 241001556359 Fusarium solani f. sp. glycines Species 0.000 description 1
- 239000005980 Gibberellic acid Substances 0.000 description 1
- 229930191978 Gibberellin Natural products 0.000 description 1
- 241000090234 Gibellina cerealis Species 0.000 description 1
- 241000461774 Gloeosporium Species 0.000 description 1
- 241001583501 Glomeromycetes Species 0.000 description 1
- 241001595254 Gnomoniopsis fructicola Species 0.000 description 1
- 241001087493 Golovinomyces Species 0.000 description 1
- 241000578422 Graphosoma lineatum Species 0.000 description 1
- 241000222684 Grifola Species 0.000 description 1
- 241000208818 Helianthus Species 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 240000001194 Heliotropium europaeum Species 0.000 description 1
- 241000509374 Heterorhabditis megidis Species 0.000 description 1
- 241001155151 Heterorhabdus Species 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- QVXFGVVYTKZLJN-UHFFFAOYSA-N Hexalure Natural products CCCCCCCCC=CCCCCCCOC(C)=O QVXFGVVYTKZLJN-UHFFFAOYSA-N 0.000 description 1
- 235000001018 Hibiscus sabdariffa Nutrition 0.000 description 1
- 240000004153 Hibiscus sabdariffa Species 0.000 description 1
- 241000908130 Hippodamia convergens Species 0.000 description 1
- 241001392799 Hippodamia variegata Species 0.000 description 1
- 101000641031 Homo sapiens Deoxynucleoside triphosphate triphosphohydrolase SAMHD1 Proteins 0.000 description 1
- 101000834981 Homo sapiens Testis, prostate and placenta-expressed protein Proteins 0.000 description 1
- 241000209219 Hordeum Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000008694 Humulus lupulus Nutrition 0.000 description 1
- 244000025221 Humulus lupulus Species 0.000 description 1
- LELOWRISYMNNSU-UHFFFAOYSA-N Hydrocyanic acid Natural products N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 1
- 241000748095 Hymenopappus filifolius Species 0.000 description 1
- 241001237548 Hymenoscyphus fraxineus Species 0.000 description 1
- 241001237941 Hypholoma Species 0.000 description 1
- KOTOUBGHZHWCCJ-UHFFFAOYSA-N IPSP Chemical compound CCS(=O)CSP(=S)(OC(C)C)OC(C)C KOTOUBGHZHWCCJ-UHFFFAOYSA-N 0.000 description 1
- 239000005795 Imazalil Substances 0.000 description 1
- XVOKUMIPKHGGTN-UHFFFAOYSA-N Imazethapyr Chemical compound OC(=O)C1=CC(CC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 XVOKUMIPKHGGTN-UHFFFAOYSA-N 0.000 description 1
- LFVLUOAHQIVABZ-UHFFFAOYSA-N Iodofenphos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(I)C=C1Cl LFVLUOAHQIVABZ-UHFFFAOYSA-N 0.000 description 1
- 235000021506 Ipomoea Nutrition 0.000 description 1
- 241000207783 Ipomoea Species 0.000 description 1
- 239000005798 Isofetamid Substances 0.000 description 1
- PIWKPBJCKXDKJR-UHFFFAOYSA-N Isoflurane Chemical compound FC(F)OC(Cl)C(F)(F)F PIWKPBJCKXDKJR-UHFFFAOYSA-N 0.000 description 1
- 239000005571 Isoxaflutole Substances 0.000 description 1
- QTGIYXFCSKXKMO-UHFFFAOYSA-N Japonilure Natural products CCCCCCCCC=CC1CCC(=O)O1 QTGIYXFCSKXKMO-UHFFFAOYSA-N 0.000 description 1
- 241000758791 Juglandaceae Species 0.000 description 1
- 241000721662 Juniperus Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- FAIXYKHYOGVFKA-UHFFFAOYSA-N Kinetin Natural products N=1C=NC=2N=CNC=2C=1N(C)C1=CC=CO1 FAIXYKHYOGVFKA-UHFFFAOYSA-N 0.000 description 1
- 239000005517 L01XE01 - Imatinib Substances 0.000 description 1
- 241000323178 Labyrinthula zosterae Species 0.000 description 1
- 241000218187 Lachnum Species 0.000 description 1
- 235000013628 Lantana involucrata Nutrition 0.000 description 1
- 240000005183 Lantana involucrata Species 0.000 description 1
- 241001575108 Latipes Species 0.000 description 1
- 244000165082 Lavanda vera Species 0.000 description 1
- 235000010663 Lavandula angustifolia Nutrition 0.000 description 1
- 240000004322 Lens culinaris Species 0.000 description 1
- 235000014647 Lens culinaris subsp culinaris Nutrition 0.000 description 1
- 241000340221 Leptomastix Species 0.000 description 1
- 241000340222 Leptomastix dactylopii Species 0.000 description 1
- 241000192132 Leuconostoc Species 0.000 description 1
- 241000896221 Leveillula taurica Species 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 241000209082 Lolium Species 0.000 description 1
- 235000002262 Lycopersicon Nutrition 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 241001414826 Lygus Species 0.000 description 1
- 241000227175 Lyonia Species 0.000 description 1
- 241001344131 Magnaporthe grisea Species 0.000 description 1
- 241001330975 Magnaporthe oryzae Species 0.000 description 1
- 239000005983 Maleic hydrazide Substances 0.000 description 1
- BGRDGMRNKXEXQD-UHFFFAOYSA-N Maleic hydrazide Chemical compound OC1=CC=C(O)N=N1 BGRDGMRNKXEXQD-UHFFFAOYSA-N 0.000 description 1
- 244000081841 Malus domestica Species 0.000 description 1
- 244000070406 Malus silvestris Species 0.000 description 1
- 241000407128 Marssonia Species 0.000 description 1
- 241001576503 Mellea Species 0.000 description 1
- 241001143352 Meloidogyne Species 0.000 description 1
- 244000246386 Mentha pulegium Species 0.000 description 1
- 235000016257 Mentha pulegium Nutrition 0.000 description 1
- 235000004357 Mentha x piperita Nutrition 0.000 description 1
- 239000005805 Mepanipyrim Substances 0.000 description 1
- 239000005807 Metalaxyl Substances 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-M Methanesulfonate Chemical compound CS([O-])(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 description 1
- 239000005916 Methomyl Substances 0.000 description 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
- 239000005810 Metrafenone Substances 0.000 description 1
- 241000192041 Micrococcus Species 0.000 description 1
- 241000192701 Microcystis Species 0.000 description 1
- 241001022799 Microdochium sorghi Species 0.000 description 1
- 241001116775 Microsorum Species 0.000 description 1
- 241001668538 Mollisia Species 0.000 description 1
- 235000006677 Monarda citriodora ssp. austromontana Nutrition 0.000 description 1
- 241001518729 Monilinia Species 0.000 description 1
- 241001459558 Monographella nivalis Species 0.000 description 1
- 240000005561 Musa balbisiana Species 0.000 description 1
- 235000018290 Musa x paradisiaca Nutrition 0.000 description 1
- 241000204031 Mycoplasma Species 0.000 description 1
- 241000899399 Mycovellosiella Species 0.000 description 1
- HCEJRQCEFIFCOZ-LBPRGKRZSA-N N'-[5-bromo-2-methyl-6-[(2S)-1-propoxypropan-2-yl]oxypyridin-3-yl]-N-ethyl-N-methylmethanimidamide Chemical compound BrC=1C=C(C(=NC=1O[C@H](COCCC)C)C)N=CN(C)CC HCEJRQCEFIFCOZ-LBPRGKRZSA-N 0.000 description 1
- IUOKJNROJISWRO-UHFFFAOYSA-N N-(2-cyano-3-methylbutan-2-yl)-2-(2,4-dichlorophenoxy)propanamide Chemical compound CC(C)C(C)(C#N)NC(=O)C(C)OC1=CC=C(Cl)C=C1Cl IUOKJNROJISWRO-UHFFFAOYSA-N 0.000 description 1
- CFZLNRGUBAVQNO-UHFFFAOYSA-N N-(3,5-Dichlorophenyl)succinimide Chemical compound ClC1=CC(Cl)=CC(N2C(CCC2=O)=O)=C1 CFZLNRGUBAVQNO-UHFFFAOYSA-N 0.000 description 1
- GQKJCCBWMYAKOY-HSZRJFAPSA-N N-[(2R)-2,4-dimethyl-1-phenylpentan-2-yl]-7,8-difluoroquinoline-3-carboxamide Chemical compound CC(C)C[C@](C)(Cc1ccccc1)NC(=O)c1cnc2c(F)c(F)ccc2c1 GQKJCCBWMYAKOY-HSZRJFAPSA-N 0.000 description 1
- RQQOBSVFTXVGRY-HSZRJFAPSA-N N-[(2R)-2,4-dimethyl-1-phenylpentan-2-yl]-8-fluoroquinoline-3-carboxamide Chemical compound CC(C)C[C@](C)(Cc1ccccc1)NC(=O)c1cnc2c(F)cccc2c1 RQQOBSVFTXVGRY-HSZRJFAPSA-N 0.000 description 1
- GQKJCCBWMYAKOY-QHCPKHFHSA-N N-[(2S)-2,4-dimethyl-1-phenylpentan-2-yl]-7,8-difluoroquinoline-3-carboxamide Chemical compound CC(C)C[C@@](C)(Cc1ccccc1)NC(=O)c1cnc2c(F)c(F)ccc2c1 GQKJCCBWMYAKOY-QHCPKHFHSA-N 0.000 description 1
- RQQOBSVFTXVGRY-QHCPKHFHSA-N N-[(2S)-2,4-dimethyl-1-phenylpentan-2-yl]-8-fluoroquinoline-3-carboxamide Chemical compound C(C1=CC=CC=C1)[C@@](CC(C)C)(C)NC(=O)C=1C=NC2=C(C=CC=C2C=1)F RQQOBSVFTXVGRY-QHCPKHFHSA-N 0.000 description 1
- XDYYWNJGHXBYGU-UHFFFAOYSA-N N-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzenecarbothioamide Chemical compound CNC(=S)C1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F XDYYWNJGHXBYGU-UHFFFAOYSA-N 0.000 description 1
- JMPFSEBWVLAJKM-UHFFFAOYSA-N N-{5-chloro-4-[(4-chlorophenyl)(cyano)methyl]-2-methylphenyl}-2-hydroxy-3,5-diiodobenzamide Chemical compound ClC=1C=C(NC(=O)C=2C(=C(I)C=C(I)C=2)O)C(C)=CC=1C(C#N)C1=CC=C(Cl)C=C1 JMPFSEBWVLAJKM-UHFFFAOYSA-N 0.000 description 1
- 241000690745 Neides Species 0.000 description 1
- 241000244206 Nematoda Species 0.000 description 1
- 241000407900 Neodiprion lecontei Species 0.000 description 1
- FQTLCLSUCSAZDY-ATGUSINASA-N Nerolidol Chemical compound CC(C)=CCC\C(C)=C\CC[C@](C)(O)C=C FQTLCLSUCSAZDY-ATGUSINASA-N 0.000 description 1
- 241000208125 Nicotiana Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 241000749985 Nites Species 0.000 description 1
- QMGVPVSNSZLJIA-UHFFFAOYSA-N Nux Vomica Natural products C1C2C3C4N(C=5C6=CC=CC=5)C(=O)CC3OCC=C2CN2C1C46CC2 QMGVPVSNSZLJIA-UHFFFAOYSA-N 0.000 description 1
- 235000010676 Ocimum basilicum Nutrition 0.000 description 1
- 240000007926 Ocimum gratissimum Species 0.000 description 1
- 241000896238 Oidium Species 0.000 description 1
- 241000795633 Olea <sea slug> Species 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004100 Oxytetracycline Substances 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- SQLZTJOKZCEAJN-UHFFFAOYSA-N P(=O)(O)(O)O.C(CCC)C1=NC=CC=N1 Chemical compound P(=O)(O)(O)O.C(CCC)C1=NC=CC=N1 SQLZTJOKZCEAJN-UHFFFAOYSA-N 0.000 description 1
- 241000235652 Pachysolen Species 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000008753 Papaver somniferum Nutrition 0.000 description 1
- 240000001090 Papaver somniferum Species 0.000 description 1
- 241000736122 Parastagonospora nodorum Species 0.000 description 1
- 241000219099 Parthenocissus quinquefolia Species 0.000 description 1
- 235000009388 Parthenocissus quinquefolia Nutrition 0.000 description 1
- 241000222291 Passalora fulva Species 0.000 description 1
- 206010034133 Pathogen resistance Diseases 0.000 description 1
- 101150003085 Pdcl gene Proteins 0.000 description 1
- 241000588701 Pectobacterium carotovorum Species 0.000 description 1
- 239000006002 Pepper Substances 0.000 description 1
- 241001670201 Peronospora destructor Species 0.000 description 1
- 244000062780 Petroselinum sativum Species 0.000 description 1
- 241001460666 Pezicula Species 0.000 description 1
- 241000440444 Phakopsora Species 0.000 description 1
- 241000222385 Phanerochaete Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 244000309557 Phyllachora pomigena Species 0.000 description 1
- 241000519856 Phyllosticta Species 0.000 description 1
- 241000210649 Phyllosticta ampelicida Species 0.000 description 1
- 241000275067 Phyllotreta Species 0.000 description 1
- 241001115351 Physalospora Species 0.000 description 1
- 241000471406 Physoderma maydis Species 0.000 description 1
- 241000263678 Phytophthora cactorum var. applanata Species 0.000 description 1
- 241000233616 Phytophthora capsici Species 0.000 description 1
- 241000233618 Phytophthora cinnamomi Species 0.000 description 1
- 241000233645 Phytophthora nicotianae Species 0.000 description 1
- 241000948155 Phytophthora sojae Species 0.000 description 1
- 239000005595 Picloram Substances 0.000 description 1
- 235000016761 Piper aduncum Nutrition 0.000 description 1
- 240000003889 Piper guineense Species 0.000 description 1
- 235000017804 Piper guineense Nutrition 0.000 description 1
- 235000008184 Piper nigrum Nutrition 0.000 description 1
- 240000006711 Pistacia vera Species 0.000 description 1
- 241000219843 Pisum Species 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 241001503464 Plasmodiophora Species 0.000 description 1
- 241000233626 Plasmopara Species 0.000 description 1
- 241000124058 Plectosphaerella Species 0.000 description 1
- 241000222351 Pleurotus cornucopiae Species 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 101100505672 Podospora anserina grisea gene Proteins 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- JPFWJDMDPLEUBD-UHFFFAOYSA-N Polyoxin D Natural products OC1C(O)C(C(NC(=O)C(C(O)C(O)COC(N)=O)N)C(O)=O)OC1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-UHFFFAOYSA-N 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241000219000 Populus Species 0.000 description 1
- 235000000497 Primula Nutrition 0.000 description 1
- 241000245063 Primula Species 0.000 description 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- UEKQGZQLUMSLNW-UHFFFAOYSA-N Propyl isome Chemical compound C1=C2C(C(=O)OCCC)C(C(=O)OCCC)C(C)CC2=CC2=C1OCO2 UEKQGZQLUMSLNW-UHFFFAOYSA-N 0.000 description 1
- 239000005824 Proquinazid Substances 0.000 description 1
- 235000009827 Prunus armeniaca Nutrition 0.000 description 1
- 244000018633 Prunus armeniaca Species 0.000 description 1
- 235000006029 Prunus persica var nucipersica Nutrition 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- 244000017714 Prunus persica var. nucipersica Species 0.000 description 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 1
- 241000589615 Pseudomonas syringae Species 0.000 description 1
- 241001281802 Pseudoperonospora Species 0.000 description 1
- 241000812329 Pseudopyrenochaeta lycopersici Species 0.000 description 1
- 241000540505 Puccinia dispersa f. sp. tritici Species 0.000 description 1
- 241000221301 Puccinia graminis Species 0.000 description 1
- 241000228453 Pyrenophora Species 0.000 description 1
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 1
- 241000231139 Pyricularia Species 0.000 description 1
- RRKHIAYNPVQKEF-UHFFFAOYSA-N Pyriftalid Chemical compound COC1=CC(OC)=NC(SC=2C=3C(=O)OC(C)C=3C=CC=2)=N1 RRKHIAYNPVQKEF-UHFFFAOYSA-N 0.000 description 1
- 239000005828 Pyrimethanil Substances 0.000 description 1
- MWMQNVGAHVXSPE-UHFFFAOYSA-N Pyriprole Chemical compound ClC=1C=C(C(F)(F)F)C=C(Cl)C=1N1N=C(C#N)C(SC(F)F)=C1NCC1=CC=CC=N1 MWMQNVGAHVXSPE-UHFFFAOYSA-N 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- 240000001987 Pyrus communis Species 0.000 description 1
- 241000918585 Pythium aphanidermatum Species 0.000 description 1
- 241001622914 Pythium arrhenomanes Species 0.000 description 1
- 241001505297 Pythium irregulare Species 0.000 description 1
- 241000918584 Pythium ultimum Species 0.000 description 1
- 240000003085 Quassia amara Species 0.000 description 1
- 235000009694 Quassia amara Nutrition 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 108020004511 Recombinant DNA Proteins 0.000 description 1
- 244000153955 Reynoutria sachalinensis Species 0.000 description 1
- 235000003202 Reynoutria sachalinensis Nutrition 0.000 description 1
- 244000299790 Rheum rhabarbarum Species 0.000 description 1
- 235000009411 Rheum rhabarbarum Nutrition 0.000 description 1
- 241000223667 Rhinocladiella Species 0.000 description 1
- 241001361634 Rhizoctonia Species 0.000 description 1
- 241000120541 Rhizophora Species 0.000 description 1
- 240000005384 Rhizopus oryzae Species 0.000 description 1
- 235000013752 Rhizopus oryzae Nutrition 0.000 description 1
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 1
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical compound N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 description 1
- 244000178231 Rosmarinus officinalis Species 0.000 description 1
- 240000007651 Rubus glaucus Species 0.000 description 1
- 241000605385 Ruscus Species 0.000 description 1
- 229930001406 Ryanodine Natural products 0.000 description 1
- PNAAEIYEUKNTMO-UHFFFAOYSA-N S-Seven Chemical compound C=1C=CC=CC=1P(=S)(OCC)OC1=CC=C(Cl)C=C1Cl PNAAEIYEUKNTMO-UHFFFAOYSA-N 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 241000447727 Scabies Species 0.000 description 1
- 241000576755 Sclerotia Species 0.000 description 1
- 241001518705 Sclerotinia minor Species 0.000 description 1
- 241000545593 Scolytinae Species 0.000 description 1
- 241001419723 Scopolia carniolica Species 0.000 description 1
- 241000239226 Scorpiones Species 0.000 description 1
- 235000007238 Secale cereale Nutrition 0.000 description 1
- 244000082988 Secale cereale Species 0.000 description 1
- 241000355135 Seimatosporium mariae Species 0.000 description 1
- ZZMNWJVJUKMZJY-AFHBHXEDSA-N Sesamolin Chemical compound C1=C2OCOC2=CC([C@H]2OC[C@H]3[C@@H]2CO[C@@H]3OC2=CC=C3OCOC3=C2)=C1 ZZMNWJVJUKMZJY-AFHBHXEDSA-N 0.000 description 1
- ZZMNWJVJUKMZJY-UHFFFAOYSA-N Sesamolin Natural products C1=C2OCOC2=CC(C2OCC3C2COC3OC2=CC=C3OCOC3=C2)=C1 ZZMNWJVJUKMZJY-UHFFFAOYSA-N 0.000 description 1
- 241000533293 Sesbania emerus Species 0.000 description 1
- 241000155666 Siphonostegia Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- 244000061458 Solanum melongena Species 0.000 description 1
- 241000227724 Sphaceloma Species 0.000 description 1
- 241000554265 Sphaerias Species 0.000 description 1
- 235000009337 Spinacia oleracea Nutrition 0.000 description 1
- 244000300264 Spinacia oleracea Species 0.000 description 1
- 239000005930 Spinosad Substances 0.000 description 1
- 241000256248 Spodoptera Species 0.000 description 1
- 241001250070 Sporisorium reilianum Species 0.000 description 1
- 241000779850 Stagonospora tainanensis Species 0.000 description 1
- 241000615365 Steinera Species 0.000 description 1
- 241001523414 Steinernema glaseri Species 0.000 description 1
- 241000509389 Steinernema riobrave Species 0.000 description 1
- 241001330502 Stephania Species 0.000 description 1
- 240000001058 Sterculia urens Species 0.000 description 1
- 235000015125 Sterculia urens Nutrition 0.000 description 1
- 241000164461 Stigmina palmivora Species 0.000 description 1
- 241001279009 Strychnos toxifera Species 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005935 Sulfuryl fluoride Substances 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- IDCBOTIENDVCBQ-UHFFFAOYSA-N TEPP Chemical compound CCOP(=O)(OCC)OP(=O)(OCC)OCC IDCBOTIENDVCBQ-UHFFFAOYSA-N 0.000 description 1
- 241001385887 Tachys Species 0.000 description 1
- 241000228446 Taphrina Species 0.000 description 1
- 102100026164 Testis, prostate and placenta-expressed protein Human genes 0.000 description 1
- 244000152045 Themeda triandra Species 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- 235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 description 1
- 235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 description 1
- HFCYZXMHUIHAQI-UHFFFAOYSA-N Thidiazuron Chemical compound C=1C=CC=CC=1NC(=O)NC1=CN=NS1 HFCYZXMHUIHAQI-UHFFFAOYSA-N 0.000 description 1
- 241000721159 Thielaviopsis paradoxa Species 0.000 description 1
- 235000007303 Thymus vulgaris Nutrition 0.000 description 1
- 240000002657 Thymus vulgaris Species 0.000 description 1
- 241000722133 Tilletia Species 0.000 description 1
- 241000949476 Toona Species 0.000 description 1
- 241001409776 Tranzschelia discolor Species 0.000 description 1
- 241000243774 Trichinella Species 0.000 description 1
- 241000223261 Trichoderma viride Species 0.000 description 1
- 241000224526 Trichomonas Species 0.000 description 1
- 239000005627 Triclopyr Substances 0.000 description 1
- 239000005858 Triflumizole Substances 0.000 description 1
- 239000005994 Trinexapac Substances 0.000 description 1
- 235000019714 Triticale Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 241000267822 Trogoderma granarium Species 0.000 description 1
- 241000157352 Uncaria Species 0.000 description 1
- 241000221576 Uromyces Species 0.000 description 1
- 241001474928 Ustilaginoidea virens Species 0.000 description 1
- 241000221566 Ustilago Species 0.000 description 1
- 241000007070 Ustilago nuda Species 0.000 description 1
- 235000003095 Vaccinium corymbosum Nutrition 0.000 description 1
- 240000001717 Vaccinium macrocarpon Species 0.000 description 1
- 235000017537 Vaccinium myrtillus Nutrition 0.000 description 1
- GSQYAWMREAXBHF-UHFFFAOYSA-N Validamine Natural products NC1CC(CO)C(O)C(O)C1O GSQYAWMREAXBHF-UHFFFAOYSA-N 0.000 description 1
- 241001645362 Valsa Species 0.000 description 1
- 241000317942 Venturia <ichneumonid wasp> Species 0.000 description 1
- FVECELJHCSPHKY-UHFFFAOYSA-N Veratridine Natural products C1=C(OC)C(OC)=CC=C1C(=O)OC1C2(O)OC34CC5(O)C(CN6C(CCC(C)C6)C6(C)O)C6(O)C(O)CC5(O)C4CCC2C3(C)CC1 FVECELJHCSPHKY-UHFFFAOYSA-N 0.000 description 1
- 241001661641 Verrucosa Species 0.000 description 1
- 241000256856 Vespidae Species 0.000 description 1
- 241000219094 Vitaceae Species 0.000 description 1
- MECHNRXZTMCUDQ-UHFFFAOYSA-N Vitamin D2 Natural products C1CCC2(C)C(C(C)C=CC(C)C(C)C)CCC2C1=CC=C1CC(O)CCC1=C MECHNRXZTMCUDQ-UHFFFAOYSA-N 0.000 description 1
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 1
- 241000893385 Waitea circinata Species 0.000 description 1
- 241000589634 Xanthomonas Species 0.000 description 1
- 241000589636 Xanthomonas campestris Species 0.000 description 1
- AMTITFMUKRZZEE-UHFFFAOYSA-N Z11-16:Ald Natural products CCCCC=CCCCCCCCCCC=O AMTITFMUKRZZEE-UHFFFAOYSA-N 0.000 description 1
- 235000007244 Zea mays Nutrition 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 239000006011 Zinc phosphide Substances 0.000 description 1
- 239000005870 Ziram Substances 0.000 description 1
- 240000001102 Zoysia matrella Species 0.000 description 1
- QWMWCLHYCTXTGW-PMPSAXMXSA-N [(2S,3S)-3-(2-methylphenyl)butan-2-yl] (2S)-2-[(3-acetyloxy-4-methoxypyridine-2-carbonyl)amino]propanoate Chemical compound COc1ccnc(C(=O)N[C@@H](C)C(=O)O[C@@H](C)[C@@H](C)c2ccccc2C)c1OC(C)=O QWMWCLHYCTXTGW-PMPSAXMXSA-N 0.000 description 1
- AGEBXNZLWBQLIE-CKJXQJPGSA-N [(2S,3S)-3-(4-fluoro-2-methylphenyl)-4-methylpentan-2-yl] (2S)-2-[(3-acetyloxy-4-methoxypyridine-2-carbonyl)amino]propanoate Chemical compound COc1ccnc(C(=O)N[C@@H](C)C(=O)O[C@@H](C)[C@@H](C(C)C)c2ccc(F)cc2C)c1OC(C)=O AGEBXNZLWBQLIE-CKJXQJPGSA-N 0.000 description 1
- ZCGFNCFJTVEQIA-YZVOILCLSA-N [(2S,3S)-3-(4-fluoro-2-methylphenyl)-4-methylpentan-2-yl] (2S)-2-[(3-hydroxy-4-methoxypyridine-2-carbonyl)amino]propanoate Chemical compound C([C@H]([C@@H](OC(=O)[C@@H](NC(=O)C1=NC=CC(=C1O)OC)C)C)C1=CC=C(F)C=C1C)(C)C ZCGFNCFJTVEQIA-YZVOILCLSA-N 0.000 description 1
- QSTAJECVDAOHMF-PNLZDCPESA-N [(2S,3S)-3-(4-fluoro-2-methylphenyl)-4-methylpentan-2-yl] (2S)-2-[(4-methoxy-3-propanoyloxypyridine-2-carbonyl)amino]propanoate Chemical compound CCC(=O)Oc1c(OC)ccnc1C(=O)N[C@@H](C)C(=O)O[C@@H](C)[C@@H](C(C)C)c1ccc(F)cc1C QSTAJECVDAOHMF-PNLZDCPESA-N 0.000 description 1
- VMFXMTJCTSYHCF-HHQUSWFZSA-N [(2r,3r,4s,5r)-5-(hexylamino)-4-hydroxy-2-(hydroxymethyl)-6-[(7-hydroxy-4-oxo-1,3a,5,6,7,7a-hexahydroimidazo[4,5-c]pyridin-2-yl)amino]oxan-3-yl] carbamate Chemical compound CCCCCCN[C@@H]1[C@H](O)[C@@H](OC(N)=O)[C@@H](CO)OC1\N=C\1NC(C(=O)NCC2O)C2N/1 VMFXMTJCTSYHCF-HHQUSWFZSA-N 0.000 description 1
- QQODLKZGRKWIFG-RUTXASTPSA-N [(R)-cyano-(4-fluoro-3-phenoxyphenyl)methyl] (1S)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-RUTXASTPSA-N 0.000 description 1
- KAATUXNTWXVJKI-QPIRBTGLSA-N [(s)-cyano-(3-phenoxyphenyl)methyl] 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-QPIRBTGLSA-N 0.000 description 1
- FSAVDKDHPDSCTO-WQLSENKSSA-N [(z)-2-chloro-1-(2,4-dichlorophenyl)ethenyl] diethyl phosphate Chemical compound CCOP(=O)(OCC)O\C(=C/Cl)C1=CC=C(Cl)C=C1Cl FSAVDKDHPDSCTO-WQLSENKSSA-N 0.000 description 1
- BTKXLQSCEOHKTF-SREVYHEPSA-N [(z)-hexadec-11-enyl] acetate Chemical compound CCCC\C=C/CCCCCCCCCCOC(C)=O BTKXLQSCEOHKTF-SREVYHEPSA-N 0.000 description 1
- QVXFGVVYTKZLJN-KHPPLWFESA-N [(z)-hexadec-7-enyl] acetate Chemical compound CCCCCCCC\C=C/CCCCCCOC(C)=O QVXFGVVYTKZLJN-KHPPLWFESA-N 0.000 description 1
- MWFQAAWRPDRKDG-KOLCDFICSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)[C@H]1C(C)(C)[C@@H]1C=C(Cl)Cl MWFQAAWRPDRKDG-KOLCDFICSA-N 0.000 description 1
- UJQAHAANAPEYLR-UHFFFAOYSA-N [2-chloro-6-[2,4,6-tri(propan-2-yl)phenyl]phenyl]-dicyclohexylphosphane Chemical group CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C1=CC=CC(Cl)=C1P(C1CCCCC1)C1CCCCC1 UJQAHAANAPEYLR-UHFFFAOYSA-N 0.000 description 1
- FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 description 1
- BVOOAEDRHLPDLV-UHFFFAOYSA-N [O-][N+](N(C1=CC=CC=C1)ONC1=CC=CC=C1)=O Chemical compound [O-][N+](N(C1=CC=CC=C1)ONC1=CC=CC=C1)=O BVOOAEDRHLPDLV-UHFFFAOYSA-N 0.000 description 1
- CWVZGJORVTZXFW-UHFFFAOYSA-N [benzyl(dimethyl)silyl]methyl carbamate Chemical compound NC(=O)OC[Si](C)(C)CC1=CC=CC=C1 CWVZGJORVTZXFW-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- GDZNYEZGJAFIKA-UHFFFAOYSA-N acetoprole Chemical compound NC1=C(S(C)=O)C(C(=O)C)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl GDZNYEZGJAFIKA-UHFFFAOYSA-N 0.000 description 1
- 239000012868 active agrochemical ingredient Substances 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- QBYJBZPUGVGKQQ-SJJAEHHWSA-N aldrin Chemical compound C1[C@H]2C=C[C@@H]1[C@H]1[C@@](C3(Cl)Cl)(Cl)C(Cl)=C(Cl)[C@@]3(Cl)[C@H]12 QBYJBZPUGVGKQQ-SJJAEHHWSA-N 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940024113 allethrin Drugs 0.000 description 1
- 235000020224 almond Nutrition 0.000 description 1
- UPEZCKBFRMILAV-UHFFFAOYSA-N alpha-Ecdysone Natural products C1C(O)C(O)CC2(C)C(CCC3(C(C(C(O)CCC(C)(C)O)C)CCC33O)C)C3=CC(=O)C21 UPEZCKBFRMILAV-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical group 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- KJBRXNXZODWCMC-UHFFFAOYSA-N anisiflupurin Chemical compound COC1=CC=CC(NC=2C=3NC=NC=3N=C(F)N=2)=C1 KJBRXNXZODWCMC-UHFFFAOYSA-N 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- PXZAWHSJYIECNQ-UHFFFAOYSA-N apholate Chemical compound C1CN1P1(N2CC2)=NP(N2CC2)(N2CC2)=NP(N2CC2)(N2CC2)=N1 PXZAWHSJYIECNQ-UHFFFAOYSA-N 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- RRZXIRBKKLTSOM-XPNPUAGNSA-N avermectin B1a Chemical compound C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 RRZXIRBKKLTSOM-XPNPUAGNSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 229950006402 benoxafos Drugs 0.000 description 1
- YFXPPSKYMBTNAV-UHFFFAOYSA-N bensultap Chemical compound C=1C=CC=CC=1S(=O)(=O)SCC(N(C)C)CSS(=O)(=O)C1=CC=CC=C1 YFXPPSKYMBTNAV-UHFFFAOYSA-N 0.000 description 1
- VVSLYIKSEBPRSN-PELKAZGASA-N benthiavalicarb Chemical compound C1=C(F)C=C2SC([C@@H](C)NC(=O)[C@@H](NC(O)=O)C(C)C)=NC2=C1 VVSLYIKSEBPRSN-PELKAZGASA-N 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- JYZIHLWOWKMNNX-UHFFFAOYSA-N benzimidazole Chemical compound C1=C[CH]C2=NC=NC2=C1 JYZIHLWOWKMNNX-UHFFFAOYSA-N 0.000 description 1
- NKDFYOWSKOHCCO-UHFFFAOYSA-N beta-ecdysone Natural products C1C(O)C(O)CC2(C)C(CCC3(C(C(C)(O)C(O)CCC(C)(O)C)CCC33O)C)C3=CC(=O)C21 NKDFYOWSKOHCCO-UHFFFAOYSA-N 0.000 description 1
- OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 235000021029 blackberry Nutrition 0.000 description 1
- 229930189065 blasticidin Natural products 0.000 description 1
- 201000000053 blastoma Diseases 0.000 description 1
- 235000021014 blueberries Nutrition 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 229940116229 borneol Drugs 0.000 description 1
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
- FNXLCIKXHOPCKH-UHFFFAOYSA-N bromamine Chemical compound BrN FNXLCIKXHOPCKH-UHFFFAOYSA-N 0.000 description 1
- XCEUHXVTRJQJSR-UHFFFAOYSA-N bromo(phenyl)phosphane Chemical compound BrPC1=CC=CC=C1 XCEUHXVTRJQJSR-UHFFFAOYSA-N 0.000 description 1
- 229960003168 bronopol Drugs 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 229960002092 busulfan Drugs 0.000 description 1
- QLHULAHOXSSASE-UHFFFAOYSA-N butan-2-yl 2-(2-hydroxyethyl)piperidine-1-carboxylate Chemical compound CCC(C)OC(=O)N1CCCCC1CCO QLHULAHOXSSASE-UHFFFAOYSA-N 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- DJIBHHGQPSAZCY-UHFFFAOYSA-N butoxy-bis(butylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound CCCCOP(=S)(SCCCC)SCCCC DJIBHHGQPSAZCY-UHFFFAOYSA-N 0.000 description 1
- HBVUDJVVVFGZMB-UHFFFAOYSA-N butyl 3-methylquinoline-4-carboxylate Chemical group C1=CC=C2C(C(=O)OCCCC)=C(C)C=NC2=C1 HBVUDJVVVFGZMB-UHFFFAOYSA-N 0.000 description 1
- DLIJPAHLBJIQHE-UHFFFAOYSA-N butylphosphane Chemical compound CCCCP DLIJPAHLBJIQHE-UHFFFAOYSA-N 0.000 description 1
- 235000001046 cacaotero Nutrition 0.000 description 1
- KXRPCFINVWWFHQ-UHFFFAOYSA-N cadusafos Chemical compound CCC(C)SP(=O)(OCC)SC(C)CC KXRPCFINVWWFHQ-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229940103357 calcium arsenate Drugs 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- NLKUPINTOLSSLD-UHFFFAOYSA-L calcium;4-(1-oxidopropylidene)-3,5-dioxocyclohexane-1-carboxylate Chemical compound [Ca+2].CCC([O-])=C1C(=O)CC(C([O-])=O)CC1=O NLKUPINTOLSSLD-UHFFFAOYSA-L 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000006013 carbendazim Substances 0.000 description 1
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 235000020226 cashew nut Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- UWGBIKPRXRSRNM-UHFFFAOYSA-N cevadine Natural products CC=C(C)/C(=O)OC1CCC2(C)C3CCC4C5(O)CC(O)C6(O)C(CN7CC(C)CCC7C6(C)O)C5(O)CC24OCC13O UWGBIKPRXRSRNM-UHFFFAOYSA-N 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 230000003559 chemosterilizing effect Effects 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
- BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 description 1
- PFIADAMVCJPXSF-UHFFFAOYSA-N chloroneb Chemical compound COC1=CC(Cl)=C(OC)C=C1Cl PFIADAMVCJPXSF-UHFFFAOYSA-N 0.000 description 1
- NZNRRXXETLSZRO-UHFFFAOYSA-N chlorthion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(Cl)=C1 NZNRRXXETLSZRO-UHFFFAOYSA-N 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- FCSHDIVRCWTZOX-DVTGEIKXSA-N clobetasol Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)CCl)(O)[C@@]1(C)C[C@@H]2O FCSHDIVRCWTZOX-DVTGEIKXSA-N 0.000 description 1
- 229960002842 clobetasol Drugs 0.000 description 1
- YUIKUTLBPMDDNQ-MRVPVSSYSA-N clodinafop Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=NC=C(Cl)C=C1F YUIKUTLBPMDDNQ-MRVPVSSYSA-N 0.000 description 1
- GKIRPKYJQBWNGO-OCEACIFDSA-N clomifene Chemical compound C1=CC(OCCN(CC)CC)=CC=C1C(\C=1C=CC=CC=1)=C(\Cl)C1=CC=CC=C1 GKIRPKYJQBWNGO-OCEACIFDSA-N 0.000 description 1
- 229960003608 clomifene Drugs 0.000 description 1
- 229950004178 closantel Drugs 0.000 description 1
- 239000007931 coated granule Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000007891 compressed tablet Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910001956 copper hydroxide Inorganic materials 0.000 description 1
- 229940120693 copper naphthenate Drugs 0.000 description 1
- SVOAENZIOKPANY-CVBJKYQLSA-L copper;(z)-octadec-9-enoate Chemical compound [Cu+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O SVOAENZIOKPANY-CVBJKYQLSA-L 0.000 description 1
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
- VNZQQAVATKSIBR-UHFFFAOYSA-L copper;octanoate Chemical compound [Cu+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O VNZQQAVATKSIBR-UHFFFAOYSA-L 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- BXNANOICGRISHX-UHFFFAOYSA-N coumaphos Chemical compound CC1=C(Cl)C(=O)OC2=CC(OP(=S)(OCC)OCC)=CC=C21 BXNANOICGRISHX-UHFFFAOYSA-N 0.000 description 1
- WBCMGDNFDRNGGZ-ACNVUDSMSA-N coumarate Natural products COC(=O)C1=CO[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]3[C@@H]1C=C[C@]34OC(=O)C(=C4)[C@H](C)OC(=O)C=Cc5ccc(O)cc5 WBCMGDNFDRNGGZ-ACNVUDSMSA-N 0.000 description 1
- 235000021019 cranberries Nutrition 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 229910001610 cryolite Inorganic materials 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- SCKHCCSZFPSHGR-UHFFFAOYSA-N cyanophos Chemical compound COP(=S)(OC)OC1=CC=C(C#N)C=C1 SCKHCCSZFPSHGR-UHFFFAOYSA-N 0.000 description 1
- XZWQKJXJNKYMAP-UHFFFAOYSA-N cyclohexen-1-ylboronic acid Chemical compound OB(O)C1=CCCCC1 XZWQKJXJNKYMAP-UHFFFAOYSA-N 0.000 description 1
- NXQGGXCHGDYOHB-UHFFFAOYSA-L cyclopenta-1,4-dien-1-yl(diphenyl)phosphane;dichloropalladium;iron(2+) Chemical group [Fe+2].Cl[Pd]Cl.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 NXQGGXCHGDYOHB-UHFFFAOYSA-L 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- LSFUGNKKPMBOMG-UHFFFAOYSA-N cycloprothrin Chemical compound ClC1(Cl)CC1(C=1C=CC=CC=1)C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 LSFUGNKKPMBOMG-UHFFFAOYSA-N 0.000 description 1
- ZXQYGBMAQZUVMI-UNOMPAQXSA-N cyhalothrin Chemical compound CC1(C)C(\C=C(/Cl)C(F)(F)F)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-UNOMPAQXSA-N 0.000 description 1
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 description 1
- 239000004062 cytokinin Substances 0.000 description 1
- UQHKFADEQIVWID-UHFFFAOYSA-N cytokinin Natural products C1=NC=2C(NCC=C(CO)C)=NC=NC=2N1C1CC(O)C(CO)O1 UQHKFADEQIVWID-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 229940100539 dibutyl adipate Drugs 0.000 description 1
- 229960002097 dibutylsuccinate Drugs 0.000 description 1
- BIXZHMJUSMUDOQ-UHFFFAOYSA-N dichloran Chemical compound NC1=C(Cl)C=C([N+]([O-])=O)C=C1Cl BIXZHMJUSMUDOQ-UHFFFAOYSA-N 0.000 description 1
- YEJGPFZQLRMXOI-PKEIRNPWSA-N diclocymet Chemical compound N#CC(C(C)(C)C)C(=O)N[C@H](C)C1=CC=C(Cl)C=C1Cl YEJGPFZQLRMXOI-PKEIRNPWSA-N 0.000 description 1
- UWQMKVBQKFHLCE-UHFFFAOYSA-N diclomezine Chemical compound C1=C(Cl)C(C)=C(Cl)C=C1C1=NNC(=O)C=C1 UWQMKVBQKFHLCE-UHFFFAOYSA-N 0.000 description 1
- 229940004812 dicloran Drugs 0.000 description 1
- LNJNFVJKDJYTEU-UHFFFAOYSA-N diethofencarb Chemical compound CCOC1=CC=C(NC(=O)OC(C)C)C=C1OCC LNJNFVJKDJYTEU-UHFFFAOYSA-N 0.000 description 1
- HQWPLXHWEZZGKY-UHFFFAOYSA-N diethylzinc Chemical compound CC[Zn]CC HQWPLXHWEZZGKY-UHFFFAOYSA-N 0.000 description 1
- NZZFYRREKKOMAT-UHFFFAOYSA-N diiodomethane Chemical compound ICI NZZFYRREKKOMAT-UHFFFAOYSA-N 0.000 description 1
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 1
- RNGDKAQQWUYBAS-UHFFFAOYSA-N dimethoxy-quinoxalin-2-yloxy-sulfanylidene-$l^{5}-phosphane Chemical group C1=CC=CC2=NC(OP(=S)(OC)OC)=CN=C21 RNGDKAQQWUYBAS-UHFFFAOYSA-N 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- FPKXBFWMIYHCID-UHFFFAOYSA-N dipymetitrone Chemical compound S1C=2C(=O)N(C)C(=O)C=2SC2=C1C(=O)N(C)C2=O FPKXBFWMIYHCID-UHFFFAOYSA-N 0.000 description 1
- ZHDBTKPXEJDTTQ-UHFFFAOYSA-N dipyrithione Chemical compound [O-][N+]1=CC=CC=C1SSC1=CC=CC=[N+]1[O-] ZHDBTKPXEJDTTQ-UHFFFAOYSA-N 0.000 description 1
- VTILJUKHXGNOHQ-UHFFFAOYSA-L disodium 2-(2-sulfonatophenoxy)benzenesulfonate Chemical compound [Na+].[Na+].S(=O)(=O)([O-])C1=C(OC2=C(C=CC=C2)S(=O)(=O)[O-])C=CC=C1 VTILJUKHXGNOHQ-UHFFFAOYSA-L 0.000 description 1
- FBELJLCOAHMRJK-UHFFFAOYSA-L disodium;2,2-bis(2-ethylhexyl)-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCC(CC)CC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CC(CC)CCCC FBELJLCOAHMRJK-UHFFFAOYSA-L 0.000 description 1
- PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 description 1
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid ester group Chemical group C(CCCCCCCCCCC)(=O)O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical class [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- QLFZZSKTJWDQOS-YDBLARSUSA-N doramectin Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C3CCCCC3)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C QLFZZSKTJWDQOS-YDBLARSUSA-N 0.000 description 1
- 229960003997 doramectin Drugs 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 210000005069 ears Anatomy 0.000 description 1
- UPEZCKBFRMILAV-JMZLNJERSA-N ecdysone Chemical compound C1[C@@H](O)[C@@H](O)C[C@]2(C)[C@@H](CC[C@@]3([C@@H]([C@@H]([C@H](O)CCC(C)(C)O)C)CC[C@]33O)C)C3=CC(=O)[C@@H]21 UPEZCKBFRMILAV-JMZLNJERSA-N 0.000 description 1
- 231100000463 ecotoxicology Toxicity 0.000 description 1
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
- 201000008184 embryoma Diseases 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 229960002125 enilconazole Drugs 0.000 description 1
- WPNHOHPRXXCPRA-TVXIRPTOSA-N eprinomectin Chemical compound O1[C@@H](C)[C@@H](NC(C)=O)[C@H](OC)C[C@@H]1O[C@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C\C=C/[C@@H]2C)\C)O[C@H]1C WPNHOHPRXXCPRA-TVXIRPTOSA-N 0.000 description 1
- 229960002346 eprinomectin Drugs 0.000 description 1
- 229960002061 ergocalciferol Drugs 0.000 description 1
- 230000000925 erythroid effect Effects 0.000 description 1
- HEZNVIYQEUHLNI-UHFFFAOYSA-N ethiofencarb Chemical compound CCSCC1=CC=CC=C1OC(=O)NC HEZNVIYQEUHLNI-UHFFFAOYSA-N 0.000 description 1
- VJYFKVYYMZPMAB-UHFFFAOYSA-N ethoprophos Chemical compound CCCSP(=O)(OCC)SCCC VJYFKVYYMZPMAB-UHFFFAOYSA-N 0.000 description 1
- KQDXOQJALDYLMO-GGWOSOGESA-N ethyl (2e,4e)-5-(1,3-benzodioxol-5-yl)penta-2,4-dienoate Chemical compound CCOC(=O)\C=C\C=C\C1=CC=C2OCOC2=C1 KQDXOQJALDYLMO-GGWOSOGESA-N 0.000 description 1
- IGUYEXXAGBDLLX-UHFFFAOYSA-N ethyl 3-(3,5-dichlorophenyl)-5-methyl-2,4-dioxo-1,3-oxazolidine-5-carboxylate Chemical compound O=C1C(C(=O)OCC)(C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 IGUYEXXAGBDLLX-UHFFFAOYSA-N 0.000 description 1
- WFCLYEAZTHWNEH-UHFFFAOYSA-N ethylthiocyanate Chemical compound CCSC#N WFCLYEAZTHWNEH-UHFFFAOYSA-N 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229930002886 farnesol Natural products 0.000 description 1
- 229940043259 farnesol Drugs 0.000 description 1
- LMVPQMGRYSRMIW-KRWDZBQOSA-N fenamidone Chemical compound O=C([C@@](C)(N=C1SC)C=2C=CC=CC=2)N1NC1=CC=CC=C1 LMVPQMGRYSRMIW-KRWDZBQOSA-N 0.000 description 1
- ZCJPOPBZHLUFHF-UHFFFAOYSA-N fenamiphos Chemical compound CCOP(=O)(NC(C)C)OC1=CC=C(SC)C(C)=C1 ZCJPOPBZHLUFHF-UHFFFAOYSA-N 0.000 description 1
- FKLFBQCQQYDUAM-UHFFFAOYSA-N fenpiclonil Chemical compound ClC1=CC=CC(C=2C(=CNC=2)C#N)=C1Cl FKLFBQCQQYDUAM-UHFFFAOYSA-N 0.000 description 1
- QGTOTYJSCYHYFK-RBODFLQRSA-N fenpicoxamid Chemical compound COC1=CC=NC(C(=O)N[C@@H]2C(O[C@@H](C)[C@H](OC(=O)C(C)C)[C@@H](CC=3C=CC=CC=3)C(=O)OC2)=O)=C1OCOC(=O)C(C)C QGTOTYJSCYHYFK-RBODFLQRSA-N 0.000 description 1
- WDQNIWFZKXZFAY-UHFFFAOYSA-M fentin acetate Chemical compound CC([O-])=O.C1=CC=CC=C1[Sn+](C=1C=CC=CC=1)C1=CC=CC=C1 WDQNIWFZKXZFAY-UHFFFAOYSA-M 0.000 description 1
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 1
- GOWLARCWZRESHU-AQTBWJFISA-N ferimzone Chemical compound C=1C=CC=C(C)C=1C(/C)=N\NC1=NC(C)=CC(C)=N1 GOWLARCWZRESHU-AQTBWJFISA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 244000037666 field crops Species 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- OWUZCVPRFKSBRG-UHFFFAOYSA-N flocoumafen Chemical compound OC=1OC2=CC=CC=C2C(=O)C=1C(C1=CC=CC=C1C1)CC1C(C=C1)=CC=C1OCC1=CC=C(C(F)(F)F)C=C1 OWUZCVPRFKSBRG-UHFFFAOYSA-N 0.000 description 1
- RLQJEEJISHYWON-UHFFFAOYSA-N flonicamid Chemical compound FC(F)(F)C1=CC=NC=C1C(=O)NCC#N RLQJEEJISHYWON-UHFFFAOYSA-N 0.000 description 1
- 239000004507 flowable concentrates for seed treatment Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- YOWNVPAUWYHLQX-UHFFFAOYSA-N fluazuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C(OC=2C(=CC(=CN=2)C(F)(F)F)Cl)=C1 YOWNVPAUWYHLQX-UHFFFAOYSA-N 0.000 description 1
- 229950006719 fluazuron Drugs 0.000 description 1
- ZGNITFSDLCMLGI-UHFFFAOYSA-N flubendiamide Chemical compound CC1=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C1NC(=O)C1=CC=CC(I)=C1C(=O)NC(C)(C)CS(C)(=O)=O ZGNITFSDLCMLGI-UHFFFAOYSA-N 0.000 description 1
- ABOVRDBEJDIBMZ-UHFFFAOYSA-N flucofuron Chemical compound C1=C(Cl)C(C(F)(F)F)=CC(NC(=O)NC=2C=C(C(Cl)=CC=2)C(F)(F)F)=C1 ABOVRDBEJDIBMZ-UHFFFAOYSA-N 0.000 description 1
- IPENDKRRWFURRE-UHFFFAOYSA-N fluoroimide Chemical compound C1=CC(F)=CC=C1N1C(=O)C(Cl)=C(Cl)C1=O IPENDKRRWFURRE-UHFFFAOYSA-N 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 244000000049 foliar pathogen Species 0.000 description 1
- 229960005102 foscarnet Drugs 0.000 description 1
- VUERQRKTYBIULR-UHFFFAOYSA-N fosetyl Chemical compound CCOP(O)=O VUERQRKTYBIULR-UHFFFAOYSA-N 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- UYJUZNLFJAWNEZ-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2NC3=CC=CC=C3N=2)=C1 UYJUZNLFJAWNEZ-UHFFFAOYSA-N 0.000 description 1
- ZEYJIQLVKGBLEM-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2N=C3[CH]C=CC=C3N=2)=C1 ZEYJIQLVKGBLEM-UHFFFAOYSA-N 0.000 description 1
- 244000000004 fungal plant pathogen Species 0.000 description 1
- PLHJDBGFXBMTGZ-WEVVVXLNSA-N furazolidone Chemical compound O1C([N+](=O)[O-])=CC=C1\C=N\N1C(=O)OCC1 PLHJDBGFXBMTGZ-WEVVVXLNSA-N 0.000 description 1
- 229960001625 furazolidone Drugs 0.000 description 1
- 235000004611 garlic Nutrition 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000012239 gene modification Methods 0.000 description 1
- 230000005017 genetic modification Effects 0.000 description 1
- 235000013617 genetically modified food Nutrition 0.000 description 1
- 239000003448 gibberellin Substances 0.000 description 1
- IXORZMNAPKEEDV-OBDJNFEBSA-N gibberellin A3 Chemical compound C([C@@]1(O)C(=C)C[C@@]2(C1)[C@H]1C(O)=O)C[C@H]2[C@]2(C=C[C@@H]3O)[C@H]1[C@]3(C)C(=O)O2 IXORZMNAPKEEDV-OBDJNFEBSA-N 0.000 description 1
- 229940100242 glycol stearate Drugs 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 235000021021 grapes Nutrition 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- WIFXJBMOTMKRMM-UHFFFAOYSA-N halfenprox Chemical compound C=1C=C(OC(F)(F)Br)C=CC=1C(C)(C)COCC(C=1)=CC=CC=1OC1=CC=CC=C1 WIFXJBMOTMKRMM-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 235000008216 herbs Nutrition 0.000 description 1
- 238000009904 heterogeneous catalytic hydrogenation reaction Methods 0.000 description 1
- NSCKKHGFMYTPBG-UHFFFAOYSA-N hexadecyl cyclopropanecarboxylate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C1CC1 NSCKKHGFMYTPBG-UHFFFAOYSA-N 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- ALBYIUDWACNRRB-UHFFFAOYSA-N hexanamide Chemical compound CCCCCC(N)=O ALBYIUDWACNRRB-UHFFFAOYSA-N 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- KTUFNOKKBVMGRW-UHFFFAOYSA-N imatinib Chemical compound C1CN(C)CCN1CC1=CC=C(C(=O)NC=2C=C(NC=3N=C(C=CN=3)C=3C=NC=CC=3)C(C)=CC=2)C=C1 KTUFNOKKBVMGRW-UHFFFAOYSA-N 0.000 description 1
- 229960002411 imatinib Drugs 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- DSXOWZNZGWXWMX-UHFFFAOYSA-N ipflufenoquin Chemical compound CC1=NC2=C(F)C(F)=CC=C2C=C1OC1=CC=CC(F)=C1C(C)(C)O DSXOWZNZGWXWMX-UHFFFAOYSA-N 0.000 description 1
- 229910000398 iron phosphate Inorganic materials 0.000 description 1
- WBJZTOZJJYAKHQ-UHFFFAOYSA-K iron(3+) phosphate Chemical compound [Fe+3].[O-]P([O-])([O-])=O WBJZTOZJJYAKHQ-UHFFFAOYSA-K 0.000 description 1
- YFVOXLJXJBQDEF-UHFFFAOYSA-N isocarbophos Chemical compound COP(N)(=S)OC1=CC=CC=C1C(=O)OC(C)C YFVOXLJXJBQDEF-UHFFFAOYSA-N 0.000 description 1
- WMKZDPFZIZQROT-UHFFFAOYSA-N isofetamid Chemical compound CC1=CC(OC(C)C)=CC=C1C(=O)C(C)(C)NC(=O)C1=C(C)C=CS1 WMKZDPFZIZQROT-UHFFFAOYSA-N 0.000 description 1
- 229960002725 isoflurane Drugs 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 150000003854 isothiazoles Chemical class 0.000 description 1
- 229940088649 isoxaflutole Drugs 0.000 description 1
- OYIKARCXOQLFHF-UHFFFAOYSA-N isoxaflutole Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C1=C(C2CC2)ON=C1 OYIKARCXOQLFHF-UHFFFAOYSA-N 0.000 description 1
- UGWALRUNBSBTGI-ZKMZRDRYSA-N kadethrin Chemical compound C(/[C@@H]1C([C@@H]1C(=O)OCC=1C=C(CC=2C=CC=CC=2)OC=1)(C)C)=C1/CCSC1=O UGWALRUNBSBTGI-ZKMZRDRYSA-N 0.000 description 1
- QANMHLXAZMSUEX-UHFFFAOYSA-N kinetin Chemical compound N=1C=NC=2N=CNC=2C=1NCC1=CC=CO1 QANMHLXAZMSUEX-UHFFFAOYSA-N 0.000 description 1
- 229960001669 kinetin Drugs 0.000 description 1
- 229930195027 lapatin Natural products 0.000 description 1
- 239000001102 lavandula vera Substances 0.000 description 1
- 235000018219 lavender Nutrition 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 230000002015 leaf growth Effects 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 235000021374 legumes Nutrition 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229960002809 lindane Drugs 0.000 description 1
- SHTFZHTWSLHVEB-BDNRQGISSA-N lineatin Chemical compound O1C(C)(C)[C@H]2[C@@]3(C)C[C@@H]1O[C@@H]2C3 SHTFZHTWSLHVEB-BDNRQGISSA-N 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- XIGAUIHYSDTJHW-UHFFFAOYSA-N mefenacet Chemical compound N=1C2=CC=CC=C2SC=1OCC(=O)N(C)C1=CC=CC=C1 XIGAUIHYSDTJHW-UHFFFAOYSA-N 0.000 description 1
- 229940103185 mefenamate Drugs 0.000 description 1
- HYYBABOKPJLUIN-UHFFFAOYSA-N mefenamic acid Chemical compound CC1=CC=CC(NC=2C(=CC=CC=2)C(O)=O)=C1C HYYBABOKPJLUIN-UHFFFAOYSA-N 0.000 description 1
- 229960001962 mefloquine Drugs 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- CIFWZNRJIBNXRE-UHFFFAOYSA-N mepanipyrim Chemical compound CC#CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 CIFWZNRJIBNXRE-UHFFFAOYSA-N 0.000 description 1
- 229940101209 mercuric oxide Drugs 0.000 description 1
- CAUHWGTUUBORAX-IKGGRYGDSA-N metarylpicoxamid Chemical compound CCC(=O)Oc1c(OC)ccnc1C(=O)N[C@@H](C)C(=O)O[C@@H](C)[C@@H](C)c1ccccc1C CAUHWGTUUBORAX-IKGGRYGDSA-N 0.000 description 1
- NNKVPIKMPCQWCG-UHFFFAOYSA-N methamidophos Chemical compound COP(N)(=O)SC NNKVPIKMPCQWCG-UHFFFAOYSA-N 0.000 description 1
- 229960001252 methamphetamine Drugs 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- IXJOSTZEBSTPAG-UHFFFAOYSA-N methasulfocarb Chemical compound CNC(=O)SC1=CC=C(OS(C)(=O)=O)C=C1 IXJOSTZEBSTPAG-UHFFFAOYSA-N 0.000 description 1
- UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- GDYXETITFYSKSR-UHFFFAOYSA-N methyl-[(5-methyl-2-phenylpyrazol-3-yl)methyl]carbamic acid Chemical compound OC(=O)N(C)CC1=CC(C)=NN1C1=CC=CC=C1 GDYXETITFYSKSR-UHFFFAOYSA-N 0.000 description 1
- VOEYXMAFNDNNED-UHFFFAOYSA-N metolcarb Chemical compound CNC(=O)OC1=CC=CC(C)=C1 VOEYXMAFNDNNED-UHFFFAOYSA-N 0.000 description 1
- AMSPWOYQQAWRRM-UHFFFAOYSA-N metrafenone Chemical compound COC1=CC=C(Br)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC AMSPWOYQQAWRRM-UHFFFAOYSA-N 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 229940124561 microbicide Drugs 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 230000000051 modifying effect Effects 0.000 description 1
- WLLGXSLBOPFWQV-OTHKPKEBSA-N molport-035-783-878 Chemical compound C([C@H]1C=C2)[C@H]2C2C1C(=O)N(CC(CC)CCCC)C2=O WLLGXSLBOPFWQV-OTHKPKEBSA-N 0.000 description 1
- KRTSDMXIXPKRQR-AATRIKPKSA-N monocrotophos Chemical compound CNC(=O)\C=C(/C)OP(=O)(OC)OC KRTSDMXIXPKRQR-AATRIKPKSA-N 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- YZBLFMPOMVTDJY-CBYMMZEQSA-N moxidectin Chemical compound O1[C@H](C(\C)=C\C(C)C)[C@@H](C)C(=N/OC)\C[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 YZBLFMPOMVTDJY-CBYMMZEQSA-N 0.000 description 1
- 229960004816 moxidectin Drugs 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- YWWVWXASSLXJHU-WAYWQWQTSA-N myristoleic acid Chemical compound CCCC\C=C/CCCCCCCC(O)=O YWWVWXASSLXJHU-WAYWQWQTSA-N 0.000 description 1
- XFGGMWATACYBEU-UHFFFAOYSA-N n'-[4-[(4,5-dichloro-1,3-thiazol-2-yl)oxy]-2,5-dimethylphenyl]-n-ethyl-n-methylmethanimidamide Chemical compound C1=C(C)C(N=CN(C)CC)=CC(C)=C1OC1=NC(Cl)=C(Cl)S1 XFGGMWATACYBEU-UHFFFAOYSA-N 0.000 description 1
- BETVNUCOOCCCIO-UHFFFAOYSA-N n-(2-dimethoxyphosphinothioylsulfanylethyl)acetamide Chemical compound COP(=S)(OC)SCCNC(C)=O BETVNUCOOCCCIO-UHFFFAOYSA-N 0.000 description 1
- COHTVILOUURPNC-UHFFFAOYSA-N n-(3,4-dichlorophenyl)-4-hydroxy-1,3-dimethyl-2,6-dioxopyrimidine-5-carboxamide Chemical compound O=C1N(C)C(=O)N(C)C(O)=C1C(=O)NC1=CC=C(Cl)C(Cl)=C1 COHTVILOUURPNC-UHFFFAOYSA-N 0.000 description 1
- DEBMUZVVCQOQFN-UHFFFAOYSA-N n-[2-(2,4-dichlorophenoxy)phenyl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1OC1=CC=C(Cl)C=C1Cl DEBMUZVVCQOQFN-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- NZPKARLAFLAVLO-UHFFFAOYSA-N n-[bis(aziridin-1-yl)phosphinothioyl]methanamine Chemical compound C1CN1P(=S)(NC)N1CC1 NZPKARLAFLAVLO-UHFFFAOYSA-N 0.000 description 1
- XBXCNNQPRYLIDE-UHFFFAOYSA-M n-tert-butylcarbamate Chemical compound CC(C)(C)NC([O-])=O XBXCNNQPRYLIDE-UHFFFAOYSA-M 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- WASNIKZYIWZQIP-AWEZNQCLSA-N nerolidol Natural products CC(=CCCC(=CCC[C@@H](O)C=C)C)C WASNIKZYIWZQIP-AWEZNQCLSA-N 0.000 description 1
- 239000011570 nicotinamide Substances 0.000 description 1
- 235000005152 nicotinamide Nutrition 0.000 description 1
- DCUJJWWUNKIJPH-UHFFFAOYSA-N nitrapyrin Chemical compound ClC1=CC=CC(C(Cl)(Cl)Cl)=N1 DCUJJWWUNKIJPH-UHFFFAOYSA-N 0.000 description 1
- 230000024121 nodulation Effects 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- NWRSOYAGXTXEMK-UHFFFAOYSA-N octadeca-2,13-dienyl acetate Chemical compound CCCCC=CCCCCCCCCCC=CCOC(C)=O NWRSOYAGXTXEMK-UHFFFAOYSA-N 0.000 description 1
- AZJXQVRPBZSNFN-UHFFFAOYSA-N octane-3,3-diol Chemical compound CCCCCC(O)(O)CC AZJXQVRPBZSNFN-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 238000006053 organic reaction Methods 0.000 description 1
- 230000008723 osmotic stress Effects 0.000 description 1
- WUVGKYVXCRSIQE-UHFFFAOYSA-N oxamic acid Chemical compound NC(=O)C(O)=O.NC(=O)C(O)=O WUVGKYVXCRSIQE-UHFFFAOYSA-N 0.000 description 1
- 125000005825 oxyethoxy group Chemical group [H]C([H])(O[*:1])C([H])([H])O[*:2] 0.000 description 1
- IWVCMVBTMGNXQD-PXOLEDIWSA-N oxytetracycline Chemical compound C1=CC=C2[C@](O)(C)[C@H]3[C@H](O)[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-PXOLEDIWSA-N 0.000 description 1
- 229960000625 oxytetracycline Drugs 0.000 description 1
- 235000019366 oxytetracycline Nutrition 0.000 description 1
- 150000002943 palmitic acids Chemical class 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
- RLBIQVVOMOPOHC-UHFFFAOYSA-N parathion-methyl Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1 RLBIQVVOMOPOHC-UHFFFAOYSA-N 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- WBTYBAGIHOISOQ-UHFFFAOYSA-N pent-4-en-1-yl 2-[(2-furylmethyl)(imidazol-1-ylcarbonyl)amino]butanoate Chemical compound C1=CN=CN1C(=O)N(C(CC)C(=O)OCCCC=C)CC1=CC=CO1 WBTYBAGIHOISOQ-UHFFFAOYSA-N 0.000 description 1
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 1
- 235000011197 perejil Nutrition 0.000 description 1
- MYOHNZJKOAODMX-UHFFFAOYSA-N phenyl n,n-dimethylcarbamate Chemical compound CN(C)C(=O)OC1=CC=CC=C1 MYOHNZJKOAODMX-UHFFFAOYSA-N 0.000 description 1
- HOKBIQDJCNTWST-UHFFFAOYSA-N phosphanylidenezinc;zinc Chemical compound [Zn].[Zn]=P.[Zn]=P HOKBIQDJCNTWST-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 230000000243 photosynthetic effect Effects 0.000 description 1
- 229940027411 picaridin Drugs 0.000 description 1
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 235000020233 pistachio Nutrition 0.000 description 1
- 230000008121 plant development Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 230000037039 plant physiology Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 description 1
- JPFWJDMDPLEUBD-ITJAGOAWSA-N polyoxorim Polymers O[C@@H]1[C@H](O)[C@@H]([C@H](NC(=O)[C@H]([C@H](O)[C@@H](O)COC(N)=O)N)C(O)=O)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-ITJAGOAWSA-N 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000021039 pomes Nutrition 0.000 description 1
- 229940097322 potassium arsenite Drugs 0.000 description 1
- JCBJVAJGLKENNC-UHFFFAOYSA-M potassium ethyl xanthate Chemical compound [K+].CCOC([S-])=S JCBJVAJGLKENNC-UHFFFAOYSA-M 0.000 description 1
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 1
- 229940116357 potassium thiocyanate Drugs 0.000 description 1
- HEQWEGCSZXMIJQ-UHFFFAOYSA-M potassium;oxoarsinite Chemical compound [K+].[O-][As]=O HEQWEGCSZXMIJQ-UHFFFAOYSA-M 0.000 description 1
- DWBSXHMYTSZXQL-UHFFFAOYSA-M potassium;quinolin-8-yl sulfate Chemical compound [K+].C1=CN=C2C(OS(=O)(=O)[O-])=CC=CC2=C1 DWBSXHMYTSZXQL-UHFFFAOYSA-M 0.000 description 1
- RFJPSAYWKBGVAW-UHFFFAOYSA-N precocene III Chemical compound O1C(C)(C)C=CC2=C1C=C(OCC)C(OC)=C2 RFJPSAYWKBGVAW-UHFFFAOYSA-N 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 1
- WTFXJFJYEJZMFO-UHFFFAOYSA-N propamidine Chemical compound C1=CC(C(=N)N)=CC=C1OCCCOC1=CC=C(C(N)=N)C=C1 WTFXJFJYEJZMFO-UHFFFAOYSA-N 0.000 description 1
- 229960003761 propamidine Drugs 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- ZYNFJRNPUDOPDR-SOFGYWHQSA-N propan-2-yl (e)-2-methylpent-2-enoate Chemical compound CC\C=C(/C)C(=O)OC(C)C ZYNFJRNPUDOPDR-SOFGYWHQSA-N 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 235000015136 pumpkin Nutrition 0.000 description 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 1
- 125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 description 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical compound OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 description 1
- BAUQXSYUDSNRHL-UHFFFAOYSA-N pyrimorph Chemical compound C1=CC(C(C)(C)C)=CC=C1C(C=1C=NC(Cl)=CC=1)=CC(=O)N1CCOCC1 BAUQXSYUDSNRHL-UHFFFAOYSA-N 0.000 description 1
- YBBJKCMMCRQZMA-UHFFFAOYSA-N pyrithione Chemical compound ON1C=CC=CC1=S YBBJKCMMCRQZMA-UHFFFAOYSA-N 0.000 description 1
- 229960003811 pyrithione disulfide Drugs 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 229940013788 quassia Drugs 0.000 description 1
- JYQUHIFYBATCCY-UHFFFAOYSA-N quinalphos Chemical compound C1=CC=CC2=NC(OP(=S)(OCC)OCC)=CN=C21 JYQUHIFYBATCCY-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- MRUMAIRJPMUAPZ-UHFFFAOYSA-N quinolin-8-ol;sulfuric acid Chemical compound OS(O)(=O)=O.C1=CN=C2C(O)=CC=CC2=C1 MRUMAIRJPMUAPZ-UHFFFAOYSA-N 0.000 description 1
- JTDPJYXDDYUJBS-UHFFFAOYSA-N quinoline-2-carbohydrazide Chemical compound C1=CC=CC2=NC(C(=O)NN)=CC=C21 JTDPJYXDDYUJBS-UHFFFAOYSA-N 0.000 description 1
- 235000021013 raspberries Nutrition 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000008261 resistance mechanism Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229960000329 ribavirin Drugs 0.000 description 1
- HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 description 1
- 230000002786 root growth Effects 0.000 description 1
- JJSYXNQGLHBRRK-SFEDZAPPSA-N ryanodine Chemical compound O([C@@H]1[C@]([C@@]2([C@]3(O)[C@]45O[C@@]2(O)C[C@]([C@]4(CC[C@H](C)[C@H]5O)O)(C)[C@@]31O)C)(O)C(C)C)C(=O)C1=CC=CN1 JJSYXNQGLHBRRK-SFEDZAPPSA-N 0.000 description 1
- 235000002020 sage Nutrition 0.000 description 1
- 208000005687 scabies Diseases 0.000 description 1
- BPQWCZKMOKHAJF-UHFFFAOYSA-N scheele's green Chemical compound [Cu+2].O[As]([O-])[O-] BPQWCZKMOKHAJF-UHFFFAOYSA-N 0.000 description 1
- 230000001932 seasonal effect Effects 0.000 description 1
- AFJYYKSVHJGXSN-KAJWKRCWSA-N selamectin Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1C(/C)=C/C[C@@H](O[C@]2(O[C@@H]([C@@H](C)CC2)C2CCCCC2)C2)C[C@@H]2OC(=O)[C@@H]([C@]23O)C=C(C)C(=N\O)/[C@H]3OC\C2=C/C=C/[C@@H]1C AFJYYKSVHJGXSN-KAJWKRCWSA-N 0.000 description 1
- 229960002245 selamectin Drugs 0.000 description 1
- 239000003620 semiochemical Substances 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- PTLRDCMBXHILCL-UHFFFAOYSA-M sodium arsenite Chemical compound [Na+].[O-][As]=O PTLRDCMBXHILCL-UHFFFAOYSA-M 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- JGFYQVQAXANWJU-UHFFFAOYSA-M sodium fluoroacetate Chemical compound [Na+].[O-]C(=O)CF JGFYQVQAXANWJU-UHFFFAOYSA-M 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000011655 sodium selenate Substances 0.000 description 1
- 235000018716 sodium selenate Nutrition 0.000 description 1
- 229960001881 sodium selenate Drugs 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
- HCJLVWUMMKIQIM-UHFFFAOYSA-M sodium;2,3,4,5,6-pentachlorophenolate Chemical compound [Na+].[O-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl HCJLVWUMMKIQIM-UHFFFAOYSA-M 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- LOGJGKGBKZOEKZ-UHFFFAOYSA-N sordidin Natural products O1C2(C)CC(C)C1(CC)OC(C)C2 LOGJGKGBKZOEKZ-UHFFFAOYSA-N 0.000 description 1
- 229940014213 spinosad Drugs 0.000 description 1
- 239000003206 sterilizing agent Substances 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- QTENRWWVYAAPBI-YCRXJPFRSA-N streptomycin sulfate Chemical compound OS(O)(=O)=O.OS(O)(=O)=O.OS(O)(=O)=O.CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](N=C(N)N)[C@H](O)[C@@H](N=C(N)N)[C@H](O)[C@H]1O.CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](N=C(N)N)[C@H](O)[C@@H](N=C(N)N)[C@H](O)[C@H]1O QTENRWWVYAAPBI-YCRXJPFRSA-N 0.000 description 1
- 229960005453 strychnine Drugs 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000005017 substituted alkenyl group Chemical group 0.000 description 1
- CCEKAJIANROZEO-UHFFFAOYSA-N sulfluramid Chemical compound CCNS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F CCEKAJIANROZEO-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- OBTWBSRJZRCYQV-UHFFFAOYSA-N sulfuryl difluoride Chemical compound FS(F)(=O)=O OBTWBSRJZRCYQV-UHFFFAOYSA-N 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 239000005936 tau-Fluvalinate Substances 0.000 description 1
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 1
- APMORJJNVZMVQK-UHFFFAOYSA-N tert-butyl 4-chloro-2-methylcyclohexane-1-carboxylate Chemical compound CC1CC(Cl)CCC1C(=O)OC(C)(C)C APMORJJNVZMVQK-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YJINQJFQLQIYHX-UHFFFAOYSA-N tetradec-11-enyl acetate Chemical compound CCC=CCCCCCCCCCCOC(C)=O YJINQJFQLQIYHX-UHFFFAOYSA-N 0.000 description 1
- 229960005199 tetramethrin Drugs 0.000 description 1
- OUOJIFQQBPKAMU-UHFFFAOYSA-N tetrazol-5-one Chemical compound O=C1N=NN=N1 OUOJIFQQBPKAMU-UHFFFAOYSA-N 0.000 description 1
- YTQVHRVITVLIRD-UHFFFAOYSA-L thallium sulfate Chemical compound [Tl+].[Tl+].[O-]S([O-])(=O)=O YTQVHRVITVLIRD-UHFFFAOYSA-L 0.000 description 1
- 229940119523 thallium sulfate Drugs 0.000 description 1
- 229910000374 thallium(I) sulfate Inorganic materials 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 description 1
- RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 description 1
- 229940033663 thimerosal Drugs 0.000 description 1
- ICTQUFQQEYSGGJ-UHFFFAOYSA-N thiocyclam oxalate Chemical compound OC(=O)C(O)=O.CN(C)C1CSSSC1 ICTQUFQQEYSGGJ-UHFFFAOYSA-N 0.000 description 1
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
- MBNMHBAJUNHZRE-UHFFFAOYSA-M thiosultap monosodium Chemical compound [Na+].OS(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O MBNMHBAJUNHZRE-UHFFFAOYSA-M 0.000 description 1
- 229960001196 thiotepa Drugs 0.000 description 1
- 210000001541 thymus gland Anatomy 0.000 description 1
- 239000001585 thymus vulgaris Substances 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 229960004380 tramadol Drugs 0.000 description 1
- TVYLLZQTGLZFBW-GOEBONIOSA-N tramadol Natural products COC1=CC=CC([C@@]2(O)[C@@H](CCCC2)CN(C)C)=C1 TVYLLZQTGLZFBW-GOEBONIOSA-N 0.000 description 1
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
- UZKQTCBAMSWPJD-UQCOIBPSSA-N trans-Zeatin Natural products OCC(/C)=C\CNC1=NC=NC2=C1N=CN2 UZKQTCBAMSWPJD-UQCOIBPSSA-N 0.000 description 1
- UZKQTCBAMSWPJD-FARCUNLSSA-N trans-zeatin Chemical compound OCC(/C)=C/CNC1=NC=NC2=C1N=CN2 UZKQTCBAMSWPJD-FARCUNLSSA-N 0.000 description 1
- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical compound O=C1C=NN=N1 FFSJPOPLSWBGQY-UHFFFAOYSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- IGOWHGRNPLFNDJ-UHFFFAOYSA-N tricos-9t-ene Natural products CCCCCCCCCCCCCC=CCCCCCCCC IGOWHGRNPLFNDJ-UHFFFAOYSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- RVKCCVTVZORVGD-UHFFFAOYSA-N trinexapac-ethyl Chemical group O=C1CC(C(=O)OCC)CC(=O)C1=C(O)C1CC1 RVKCCVTVZORVGD-UHFFFAOYSA-N 0.000 description 1
- SBXWFLISHPUINY-UHFFFAOYSA-N triphenyltin Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 SBXWFLISHPUINY-UHFFFAOYSA-N 0.000 description 1
- GSQYAWMREAXBHF-UOYQFSTFSA-N validamine Chemical compound N[C@H]1C[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O GSQYAWMREAXBHF-UOYQFSTFSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- FVECELJHCSPHKY-JLSHOZRYSA-N veratridine Chemical compound C1=C(OC)C(OC)=CC=C1C(=O)O[C@@H]1[C@@]2(O)O[C@]34C[C@@]5(O)[C@H](CN6[C@@H](CC[C@H](C)C6)[C@@]6(C)O)[C@]6(O)[C@@H](O)C[C@@]5(O)[C@@H]4CC[C@H]2[C@]3(C)CC1 FVECELJHCSPHKY-JLSHOZRYSA-N 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000001892 vitamin D2 Nutrition 0.000 description 1
- 239000011653 vitamin D2 Substances 0.000 description 1
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 1
- 235000005282 vitamin D3 Nutrition 0.000 description 1
- 239000011647 vitamin D3 Substances 0.000 description 1
- QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
- 229940021056 vitamin d3 Drugs 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004565 water dispersible tablet Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 241000228158 x Triticosecale Species 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
- 125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 0.000 description 1
- 229940023877 zeatin Drugs 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 229940048462 zinc phosphide Drugs 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/34—Nitriles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing within the same carbon skeleton a carboxylic group or a thio analogue, or a derivative thereof, and a carbon atom having only two bonds to hetero atoms with at the most one bond to halogen, e.g. keto-carboxylic acids
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N45/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring
- A01N45/02—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring having three carbocyclic rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- A01N47/04—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing >N—S—C≡(Hal)3 groups
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- A01N47/14—Di-thio analogues thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/02—Sulfur; Selenium; Tellurium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/16—Heavy metals; Compounds thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/16—Heavy metals; Compounds thereof
- A01N59/20—Copper
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/26—Phosphorus; Compounds thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P3/00—Fungicides
Abstract
披露了一种包含组分(A)和(B)的混合物的杀真菌组合物,其中组分(A)和(B)是如权利要求1中所定义的,以及所述组合物在农业或园艺中用于控制或预防植物被植物病原性微生物、优选真菌侵染的用途。
Description
本发明涉及新颖的杀真菌组合物,涉及它们在农业或园艺中用于控制由植物病原菌(尤其是植物病原性真菌)引起的病害的用途,并且涉及控制有用植物上的病害的方法。
尽管属于多种不同化学类别的许多杀真菌化合物和组合物已被开发或正在被开发用于在有用植物作物中作为杀真菌剂使用,但在很多方面,针对具体植物病原性真菌的作物耐受性和活性并不总能满足农业实践的需要。因此,存在如下持续需求:发现具有优异生物学特性的新化合物和组合物以用于控制或预防植物被植物病原性真菌侵染。例如,具有更大的生物活性、有利的活性谱、增加的安全性、改善的物理化学特性、增加的生物降解性的化合物。或另外,具有更宽的活性谱、改善的作物耐受性、改善的协同相互作用或增强特性的组合物,或显示更快速起效或具有更长持续残留活性或能够减少用于有效控制植物病原菌所需的化合物和组合物的施用次数和/或降低其施用率,从而能够实现有益的耐性管理实践、降低环境影响并且减少操作人员暴露的组合物。
使用包含具有不同作用模式的不同杀真菌化合物的混合物的组合物可以解决这些需要中的一些(例如通过将具有不同活性谱的杀真菌剂进行组合)。
根据本发明,提供了一种杀真菌组合物,该杀真菌组合物包含作为活性成分的组分(A)和(B)的混合物,其中组分(A)是具有式(I)的化合物
其中
R1是甲基;
R2是氢;
R3是氢;
R4是C3-C7环烷基;
或其农艺学上可接受的盐;
并且
组分(B)是选自由以下组成的组的化合物:
联苯吡菌胺、硫、氢氧化铜、氯啶菌酯、阿拉酸式苯-S-甲基(acibenzolar-S-methyl)、王铜(copper oxychloride)、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、多效唑、丙硫菌唑、咪鲜胺、丙环唑、啶菌噁唑、戊唑醇、苯锈啶(fenpropidin)、丁苯吗啉、螺环菌胺、嘧菌环胺、咯菌腈、甲霜灵、甲霜灵-M(精甲霜灵)、多菌灵、吡噻菌胺(penthiopyrad)、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、灭菌丹、百菌清、氟啶胺(fluazinam)、氟唑菌酰胺、环酰菌胺、三乙膦酸铝(fosetyl-aluminium)、吡菌苯威、三环唑、双炔酰菌胺(mandipropamid)、氟苯醚酰胺、吡唑萘菌胺(isopyrazam)、氟唑环菌胺(sedaxane)、苯并烯氟菌唑、氟唑菌酰羟胺、异氟普兰(isoflucypram)、异噻菌胺、地芬灭替松(dipymetitrone)、氟茚唑菌胺(fluindapyr)、甲香菌酯(jiaxiangjunzhi)、鲁本米西安(lvbenmixianan)、曼德斯宾(mandestrobin)、氟噻唑吡乙酮(oxathiapiprolin)、联苯吡嗪菌胺(pyraziflumid)、英派尔福沙姆(inpyrfluxam)、氯氟醚菌唑、异芬特氟克那唑(ipfentrifluconazole)、爱米诺庇力芬(aminopyrifen)、(Z,2E)-5-[1-(4-氯苯基)吡唑-3-基]氧基-2-甲氧基亚氨基-N,3-二甲基-戊-3-烯酰胺、吡啶菌酰胺、芬庇科米得(fenpicoxamid)、氟苯喹(ipflufenoquin)、奎诺福林(quinofumelin)、苯噻菌酯、氟吡菌酰胺、吡丙炔(pyrapropoyne)、2-(二氟甲基)-N-(3-乙基-1,1-二甲基-茚满-4-基)吡啶-3-甲酰胺、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈、美特尔特特拉普罗(metyltetraprole)、氟哌啶(fluoxapiprolin)、烯肟菌酯(enoxastrobin)、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(5-硫代-4H-1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈、抗倒酸(trinexapac)、抗倒酯、丁香菌酯、N'-[5-溴-2-甲基-6-[(1S)-1-甲基-2-丙氧基-乙氧基]-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-[(1R)-1-甲基-2-丙氧基-乙氧基]-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-氯-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-异丙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(2-丙氧基丙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N-异丙基-N’-[5-甲氧基-2-甲基-4-(2,2,2-三氟-1-羟基-1-苯基-乙基)苯基]-N-甲基-甲脒、N’-[4-(1-环丙基-2,2,2-三氟-1-羟基-乙基)-5-甲氧基-2-甲基-苯基]-N-异丙基-N-甲基-甲脒、N-乙基-N’-[5-甲氧基-2-甲基-4-[2-三氟甲基)氧杂环丁烷-2-基]苯基]-N-甲基-甲脒、N-乙基-N’-[5-甲氧基-2-甲基-4-[2-三氟甲基)四氢呋喃-2-基]苯基]-N-甲基-甲脒、N-(2-氟苯基)-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、N-甲氧基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]环丙烷甲酰胺、N,2-二甲氧基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、N-乙基-2-甲基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、[(1S,2S)-1-甲基-2-(邻甲苯基)丙基](2S)-2-[(4-甲氧基-3-丙酰基氧基-吡啶-2-羰基)氨基]丙酸酯、1-甲氧基-3-甲基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、1,3-二甲氧基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、3-乙基-1-甲氧基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、4,4-二甲基-2-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]异噁唑烷-3-酮、5,5-二甲基-2-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]异噁唑烷-3-酮、1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]吡唑-4-甲酸乙酯、N,N-二甲基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]-1,2,4-三唑-3-胺、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈、2-氨基-6-甲基-吡啶-3-甲酸(4-苯氧基苯基)甲酯、N-甲基-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]硫代苯甲酰胺;N-甲基-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺;(Z,2E)-5-[1-(2,4-二氯苯基)吡唑-3-基]氧基-2-甲氧基亚氨基-N,3-二甲基-戊-3-烯酰胺、(5-甲基-2-吡啶基)-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲酮、(3-甲基异噁唑-5-基)-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲酮、1-[[5-[5-(三氟甲基)-1,2,4-噁二唑-3-基]-2-噻吩基]甲基]吡唑-4-甲酸乙酯、2,2-二氟-N-甲基-2-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]乙酰胺、N-[(Z)-甲氧基亚氨基甲基]-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、N-[N-甲氧基-C-甲基-碳酰亚胺基]-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、N-[3-(4-氯苯基)-4,5-二氢异噁唑-5-基]-5-甲基-1,2,4-噁二唑-3-甲酰胺、2-(二氟甲基)-N-(1,1-二甲基-3-丙基-茚满-4-基)吡啶-3-甲酰胺、[(1S,2S)-2-(4-氟-2-甲基-苯基)-1,3-二甲基-丁基](2S)-2-[(3-乙酰氧基-4-甲氧基-吡啶-2-羰基)氨基]丙酸酯、[(1S,2S)-2-(4-氟-2-甲基-苯基)-1,3-二甲基-丁基](2S)-2-[[3-(乙酰氧基甲氧基)-4-甲氧基-吡啶-2-羰基]氨基]丙酸酯、顺式-茉莉酮、膦酸钾、膦酸钙、草甘膦(包括其二铵、异丙基铵和钾盐)、2,4-D(包括其胆碱盐和2-乙基己基酯)、麦草畏(包括其铝、氨基丙基、双-氨基丙基甲基、胆碱、1,3-二氯丙烯(dichloroprop)、二甘醇胺、二甲基胺、二甲基铵、钾和钠盐)、草铵膦(包括其铵盐)、噻虫嗪、环丁氟仑(cyclobutrifluram)、异噁唑虫酰胺、甲氧哌啶乙酯(spiropidion)、阿维菌素、埃玛菌素、溴氰虫酰胺、氯虫苯甲酰胺、丁醚脲、溴虫氟苯双酰胺(broflanilide)、2-氯-N-环丙基-5-(1-{2,6-二氯-4-[1,2,2,2-四氟-1-(三氟甲基)乙基]苯基}-1H-吡唑-4-基)-N-甲基烟酰胺和氟噁唑酰胺(fluxametamide)。
通常,组分(A)与组分(B)的重量比可以优选是从100:1至1:100、从50:1至1:50、从20:1至1:50、从15:1至1:50、从15:1至1:30、从12:1至1:25、从10:1至1:20、从5:1和1:15、从3:1至1:10或者从2:1至1:5。
另外根据本发明,提供了一种控制或预防有用植物或其繁殖材料上的植物病原性病害、尤其是植物病原性真菌的方法,该方法包括将根据本发明的杀真菌组合物施用到这些有用植物、其场所或其繁殖材料上。
由根据本发明的某些杀真菌混合物组合物提供的益处还可以尤其包括针对保护植物对抗由真菌引起的病害的有利水平的生物活性或对于用作农用化学活性成分的优越特性(例如,更大的生物活性、有利的活性谱、增加的安全性、改善的物理-化学特性、或增加的生物可降解性)。
针对在具有式(I)的化合物中取代基R1、R2、R3和R4的优选的基团和值,以其任何组合,是如以下列出的。
R1是甲基。
R2是氢。
R3是氢。
R4是C3-C7环烷基。
优选地,组分(A)是选自以下的化合物:
(Z)-2-(5-环丁基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.01),
(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.02),
(Z)-2-(5-环丙基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.03),或
(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.04),如以下表X中所定义。
更优选地,组分(A)是选自以下的化合物,
(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.02),或
(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.04),如以下表X中所定义。
在一个实施例中,组分(A)是(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.02)。
在另一个实施例中,组分(A)是(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.04)。
表X
组分(B)是选自由以下组成的组的化合物:
联苯吡菌胺、硫、氢氧化铜、氯啶菌酯、阿拉酸式苯-S-甲基、王铜、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、多效唑、丙硫菌唑、咪鲜胺、丙环唑、啶菌噁唑、戊唑醇、苯锈啶、丁苯吗啉、螺环菌胺、嘧菌环胺、咯菌腈、甲霜灵、甲霜灵-M(精甲霜灵)、多菌灵、吡噻菌胺、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、灭菌丹、百菌清、氟啶胺、氟唑菌酰胺、环酰菌胺、三乙膦酸铝、吡菌苯威、三环唑、双炔酰菌胺、氟苯醚酰胺、吡唑萘菌胺、氟唑环菌胺、苯并烯氟菌唑、氟唑菌酰羟胺、异氟普兰、异噻菌胺、地芬灭替松、氟茚唑菌胺、甲香菌酯、鲁本米西安、曼德斯宾、氟噻唑吡乙酮、联苯吡嗪菌胺、英派尔福沙姆、氯氟醚菌唑、异芬特氟克那唑、爱米诺庇力芬、(Z,2E)-5-[1-(4-氯苯基)吡唑-3-基]氧基-2-甲氧基亚氨基-N,3-二甲基-戊-3-烯酰胺、吡啶菌酰胺、芬庇科米得、氟苯喹、奎诺福林、苯噻菌酯、氟吡菌酰胺、吡丙炔、2-(二氟甲基)-N-(3-乙基-1,1-二甲基-茚满-4-基)吡啶-3-甲酰胺、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈、美特尔特特拉普罗、氟哌啶、烯肟菌酯、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(5-硫代-4H-1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈、抗倒酸、抗倒酯、丁香菌酯、N'-[5-溴-2-甲基-6-[(1S)-1-甲基-2-丙氧基-乙氧基]-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-[(1R)-1-甲基-2-丙氧基-乙氧基]-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-氯-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-异丙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(2-丙氧基丙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N-异丙基-N’-[5-甲氧基-2-甲基-4-(2,2,2-三氟-1-羟基-1-苯基-乙基)苯基]-N-甲基-甲脒、N’-[4-(1-环丙基-2,2,2-三氟-1-羟基-乙基)-5-甲氧基-2-甲基-苯基]-N-异丙基-N-甲基-甲脒、N-乙基-N’-[5-甲氧基-2-甲基-4-[2-三氟甲基)氧杂环丁烷-2-基]苯基]-N-甲基-甲脒、N-乙基-N’-[5-甲氧基-2-甲基-4-[2-三氟甲基)四氢呋喃-2-基]苯基]-N-甲基-甲脒、N-(2-氟苯基)-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、N-甲氧基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]环丙烷甲酰胺、N,2-二甲氧基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、N-乙基-2-甲基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、[(1S,2S)-1-甲基-2-(邻甲苯基)丙基](2S)-2-[(4-甲氧基-3-丙酰基氧基-吡啶-2-羰基)氨基]丙酸酯、1-甲氧基-3-甲基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、1,3-二甲氧基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、3-乙基-1-甲氧基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、4,4-二甲基-2-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]异噁唑烷-3-酮、5,5-二甲基-2-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]异噁唑烷-3-酮、1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]吡唑-4-甲酸乙酯、N,N-二甲基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]-1,2,4-三唑-3-胺、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈、2-氨基-6-甲基-吡啶-3-甲酸(4-苯氧基苯基)甲酯、N-甲基-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]硫代苯甲酰胺;N-甲基-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺;(Z,2E)-5-[1-(2,4-二氯苯基)吡唑-3-基]氧基-2-甲氧基亚氨基-N,3-二甲基-戊-3-烯酰胺、(5-甲基-2-吡啶基)-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲酮、(3-甲基异噁唑-5-基)-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲酮、1-[[5-[5-(三氟甲基)-1,2,4-噁二唑-3-基]-2-噻吩基]甲基]吡唑-4-甲酸乙酯、2,2-二氟-N-甲基-2-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]乙酰胺、N-[(Z)-甲氧基亚氨基甲基]-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、N-[N-甲氧基-C-甲基-碳酰亚胺基]-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、N-[3-(4-氯苯基)-4,5-二氢异噁唑-5-基]-5-甲基-1,2,4-噁二唑-3-甲酰胺、2-(二氟甲基)-N-(1,1-二甲基-3-丙基-茚满-4-基)吡啶-3-甲酰胺、[(1S,2S)-2-(4-氟-2-甲基-苯基)-1,3-二甲基-丁基](2S)-2-[(3-乙酰氧基-4-甲氧基-吡啶-2-羰基)氨基]丙酸酯、[(1S,2S)-2-(4-氟-2-甲基-苯基)-1,3-二甲基-丁基](2S)-2-[[3-(乙酰氧基甲氧基)-4-甲氧基-吡啶-2-羰基]氨基]丙酸酯、顺式-茉莉酮、膦酸钾、膦酸钙、草甘膦(包括其二铵、异丙基铵和钾盐)、2,4-D(包括其胆碱盐和2-乙基己基酯)、麦草畏(包括其铝、氨基丙基、双-氨基丙基甲基、胆碱、1,3-二氯丙烯、二甘醇胺、二甲基胺、二甲基铵、钾和钠盐)、草铵膦(包括其铵盐)、噻虫嗪、环丁氟仑、异噁唑虫酰胺、甲氧哌啶乙酯、阿维菌素、埃玛菌素、溴氰虫酰胺、氯虫苯甲酰胺、丁醚脲、溴虫氟苯双酰胺、2-氯-N-环丙基-5-(1-{2,6-二氯-4-[1,2,2,2-四氟-1-(三氟甲基)乙基]苯基}-1H-吡唑-4-基)-N-甲基烟酰胺和氟噁唑酰胺。
优选地,组分(B)是选自由以下组成的组的化合物:联苯吡菌胺、硫、氢氧化铜、氯啶菌酯、阿拉酸式苯-S-甲基、王铜、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、多效唑、丙硫菌唑、咪鲜胺、丙环唑、啶菌噁唑、戊唑醇、苯锈啶、丁苯吗啉、螺环菌胺、嘧菌环胺、咯菌腈、甲霜灵、甲霜灵-M(精甲霜灵)、多菌灵、吡噻菌胺、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、灭菌丹、百菌清、氟啶胺、氟唑菌酰胺、环酰菌胺、三乙膦酸铝、吡菌苯威、三环唑、双炔酰菌胺、氟苯醚酰胺、吡唑萘菌胺、氟唑环菌胺、苯并烯氟菌唑、氟唑菌酰羟胺、异氟普兰、异噻菌胺、地芬灭替松、氟茚唑菌胺、甲香菌酯、鲁本米西安、曼德斯宾、氟噻唑吡乙酮、联苯吡嗪菌胺、英派尔福沙姆、氯氟醚菌唑、异芬特氟克那唑、爱米诺庇力芬、(Z,2E)-5-[1-(4-氯苯基)吡唑-3-基]氧基-2-甲氧基亚氨基-N,3-二甲基-戊-3-烯酰胺、吡啶菌酰胺、芬庇科米得、氟苯喹、奎诺福林、苯噻菌酯、氟吡菌酰胺、吡丙炔、2-(二氟甲基)-N-(3-乙基-1,1-二甲基-茚满-4-基)吡啶-3-甲酰胺、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈、美特尔特特拉普罗、氟哌啶、烯肟菌酯、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(5-硫代-4H-1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈、抗倒酸、抗倒酯、丁香菌酯、N'-[5-溴-2-甲基-6-[(1S)-1-甲基-2-丙氧基-乙氧基]-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-[(1R)-1-甲基-2-丙氧基-乙氧基]-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-氯-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-异丙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(2-丙氧基丙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N-异丙基-N’-[5-甲氧基-2-甲基-4-(2,2,2-三氟-1-羟基-1-苯基-乙基)苯基]-N-甲基-甲脒、N’-[4-(1-环丙基-2,2,2-三氟-1-羟基-乙基)-5-甲氧基-2-甲基-苯基]-N-异丙基-N-甲基-甲脒、N-乙基-N’-[5-甲氧基-2-甲基-4-[2-三氟甲基)氧杂环丁烷-2-基]苯基]-N-甲基-甲脒、N-乙基-N’-[5-甲氧基-2-甲基-4-[2-三氟甲基)四氢呋喃-2-基]苯基]-N-甲基-甲脒、N-甲氧基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]环丙烷甲酰胺、N,2-二甲氧基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、N-乙基-2-甲基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、1-甲氧基-3-甲基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、1,3-二甲氧基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、3-乙基-1-甲氧基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、4,4-二甲基-2-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]异噁唑烷-3-酮、5,5-二甲基-2-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]异噁唑烷-3-酮、1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]吡唑-4-甲酸乙酯、N,N-二甲基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]-1,2,4-三唑-3-胺、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈、2-氨基-6-甲基-吡啶-3-甲酸(4-苯氧基苯基)甲酯、N-甲基-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]硫代苯甲酰胺;N-甲基-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺;(Z,2E)-5-[1-(2,4-二氯苯基)吡唑-3-基]氧基-2-甲氧基亚氨基-N,3-二甲基-戊-3-烯酰胺、(5-甲基-2-吡啶基)-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲酮、(3-甲基异噁唑-5-基)-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲酮、1-[[5-[5-(三氟甲基)-1,2,4-噁二唑-3-基]-2-噻吩基]甲基]吡唑-4-甲酸乙酯、2,2-二氟-N-甲基-2-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]乙酰胺、N-[(Z)-甲氧基亚氨基甲基]-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、N-[N-甲氧基-C-甲基-碳酰亚胺基]-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、N-[3-(4-氯苯基)-4,5-二氢异噁唑-5-基]-5-甲基-1,2,4-噁二唑-3-甲酰胺、2-(二氟甲基)-N-(1,1-二甲基-3-丙基-茚满-4-基)吡啶-3-甲酰胺、[(1S,2S)-2-(4-氟-2-甲基-苯基)-1,3-二甲基-丁基](2S)-2-[(3-乙酰氧基-4-甲氧基-吡啶-2-羰基)氨基]丙酸酯、[(1S,2S)-2-(4-氟-2-甲基-苯基)-1,3-二甲基-丁基](2S)-2-[[3-(乙酰氧基甲氧基)-4-甲氧基-吡啶-2-羰基]氨基]丙酸酯、顺式-茉莉酮、膦酸钾、膦酸钙、草甘膦(包括其二铵、异丙基铵和钾盐)、2,4-D(包括其胆碱盐和2-乙基己基酯)、麦草畏(包括其铝、氨基丙基、双-氨基丙基甲基、胆碱、1,3-二氯丙烯、二甘醇胺、二甲基胺、二甲基铵、钾和钠盐)、草铵膦(包括其铵盐)、噻虫嗪、环丁氟仑、异噁唑虫酰胺、甲氧哌啶乙酯、阿维菌素、埃玛菌素、溴氰虫酰胺、氯虫苯甲酰胺、丁醚脲、溴虫氟苯双酰胺、2-氯-N-环丙基-5-(1-{2,6-二氯-4-[1,2,2,2-四氟-1-(三氟甲基)乙基]苯基}-1H-吡唑-4-基)-N-甲基烟酰胺和氟噁唑酰胺。
更优选地,组分(B)是选自由以下组成的组的化合物:联苯吡菌胺、氯啶菌酯、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、丙硫菌唑、丙环唑、戊唑醇、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、百菌清、氟唑菌酰胺、吡菌苯威、苯并烯氟菌唑、异氟普兰(isoflucypram)、甲香菌酯(jiaxiangjunzhi)、曼德斯宾(mandestrobin)、氯氟醚菌唑、异芬特氟克那唑(ipfentrifluconazole)、苯噻菌酯、美特尔特特拉普罗(metyltetraprole)、烯肟菌酯(enoxastrobin)、丁香菌酯、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、和3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈。
甚至更优选地,组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰(isoflucypram)、和美特尔特特拉普罗(metyltetraprole)。
又甚至更优选地,组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、和美特尔特特拉普罗。
此外又还更优选地,组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、丙硫菌唑、嘧菌酯、肟菌酯、唑菌胺酯、和美特尔特特拉普罗(metyltetraprole)。
此外还优选地,组分(B)是嘧菌酯或肟菌酯。
最优选地,组分(B)是嘧菌酯。
在一个实施例中,组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、苯锈啶、丁苯吗啉、咯菌腈、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、灭菌丹、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰、氟唑菌酰羟胺、氯氟醚菌唑、吡啶菌酰胺、美特尔特特拉普罗、N-(2-氟苯基)-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、和[(1S,2S)-1-甲基-2-(邻甲苯基)丙基](2S)-2-[(4-甲氧基-3-丙酰基氧基-吡啶-2-羰基)氨基]丙酸酯。优选地,组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、丙硫菌唑、苯锈啶、丁苯吗啉、咯菌腈、嘧菌酯、肟菌酯、唑菌胺酯、代森锰锌、灭菌丹、百菌清、苯并烯氟菌唑、氟唑菌酰羟胺、氯氟醚菌唑、吡啶菌酰胺、美特尔特特拉普罗、N-(2-氟苯基)-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、和[(1S,2S)-1-甲基-2-(邻甲苯基)丙基](2S)-2-[(4-甲氧基-3-丙酰基氧基-吡啶-2-羰基)氨基]丙酸酯。
这些组分(B)化合物在本文和上文中是通过在个别情况下使用的所谓的“ISO通用名”或另一种“通用名”或商标名来提及。这些组分(B)化合物是已知的,并且是可商购的和/或可以使用本领域中已知的程序和/或在文献中报道的程序来制备。
在根据本发明的优选的组合物中,组分(A)是化合物编号X.01(Z)-2-(5-环丁基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:联苯吡菌胺、氯啶菌酯、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、丙硫菌唑、丙环唑、戊唑醇、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、百菌清、氟唑菌酰胺、吡菌苯威、苯并烯氟菌唑、异氟普兰(isoflucypram)、甲香菌酯(jiaxiangjunzhi)、曼德斯宾(mandestrobin)、氯氟醚菌唑、异芬特氟克那唑(ipfentrifluconazole)、苯噻菌酯、美特尔特特拉普罗(metyltetraprole)、烯肟菌酯(enoxastrobin)、丁香菌酯、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、和3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈,其中组分(A)与组分(B)的重量比是从15:1至1:50。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.02(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:联苯吡菌胺、氯啶菌酯、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、丙硫菌唑、丙环唑、戊唑醇、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、百菌清、氟唑菌酰胺、吡菌苯威、苯并烯氟菌唑、异氟普兰(isoflucypram)、甲香菌酯(jiaxiangjunzhi)、曼德斯宾(mandestrobin)、氯氟醚菌唑、异芬特氟克那唑(ipfentrifluconazole)、苯噻菌酯、美特尔特特拉普罗(metyltetraprole)、烯肟菌酯(enoxastrobin)、丁香菌酯、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、和3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈,其中组分(A)与组分(B)的重量比是从15:1至1:50。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.03(Z)-2-(5-环丙基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:联苯吡菌胺、氯啶菌酯、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、丙硫菌唑、丙环唑、戊唑醇、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、百菌清、氟唑菌酰胺、吡菌苯威、苯并烯氟菌唑、异氟普兰(isoflucypram)、甲香菌酯(jiaxiangjunzhi)、曼德斯宾(mandestrobin)、氯氟醚菌唑、异芬特氟克那唑(ipfentrifluconazole)、苯噻菌酯、美特尔特特拉普罗(metyltetraprole)、烯肟菌酯(enoxastrobin)、丁香菌酯、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、和3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈,其中组分(A)与组分(B)的重量比是从15:1至1:50。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.04(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:联苯吡菌胺、氯啶菌酯、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、丙硫菌唑、丙环唑、戊唑醇、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、百菌清、氟唑菌酰胺、吡菌苯威、苯并烯氟菌唑、异氟普兰(isoflucypram)、甲香菌酯(jiaxiangjunzhi)、曼德斯宾(mandestrobin)、氯氟醚菌唑、异芬特氟克那唑(ipfentrifluconazole)、苯噻菌酯、美特尔特特拉普罗(metyltetraprole)、烯肟菌酯(enoxastrobin)、丁香菌酯、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、和3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈,其中组分(A)与组分(B)的重量比是从15:1至1:50。
在根据本发明的更优选的组合物中,组分(A)是化合物编号X.01(Z)-2-(5-环丁基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰和美特尔特特拉普罗,其中组分(A)与组分(B)的重量比是从15:1至1:50。
在根据本发明的更优选的组合物中,组分(A)是化合物编号X.02(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰和美特尔特特拉普罗,其中组分(A)与组分(B)的重量比是从15:1至1:50。
在根据本发明的更优选的组合物中,组分(A)是化合物编号X.03(Z)-2-(5-环丙基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰和美特尔特特拉普罗,其中组分(A)与组分(B)的重量比是从15:1至1:50。
在根据本发明的更优选的组合物中,组分(A)是化合物编号X.04(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰和美特尔特特拉普罗,其中组分(A)与组分(B)的重量比是从15:1至1:50。
在根据本发明的优选的组合物中,组分(A)是化合物编号X.01(Z)-2-(5-环丁基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:联苯吡菌胺、氯啶菌酯、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、丙硫菌唑、丙环唑、戊唑醇、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、百菌清、氟唑菌酰胺、吡菌苯威、苯并烯氟菌唑、异氟普兰(isoflucypram)、甲香菌酯(jiaxiangjunzhi)、曼德斯宾(mandestrobin)、氯氟醚菌唑、异芬特氟克那唑(ipfentrifluconazole)、苯噻菌酯、美特尔特特拉普罗(metyltetraprole)、烯肟菌酯(enoxastrobin)、丁香菌酯、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、和3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈,其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.02(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:联苯吡菌胺、氯啶菌酯、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、丙硫菌唑、丙环唑、戊唑醇、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、百菌清、氟唑菌酰胺、吡菌苯威、苯并烯氟菌唑、异氟普兰(isoflucypram)、甲香菌酯(jiaxiangjunzhi)、曼德斯宾(mandestrobin)、氯氟醚菌唑、异芬特氟克那唑(ipfentrifluconazole)、苯噻菌酯、美特尔特特拉普罗(metyltetraprole)、烯肟菌酯(enoxastrobin)、丁香菌酯、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、和3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈,其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.03(Z)-2-(5-环丙基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:联苯吡菌胺、氯啶菌酯、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、丙硫菌唑、丙环唑、戊唑醇、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、百菌清、氟唑菌酰胺、吡菌苯威、苯并烯氟菌唑、异氟普兰(isoflucypram)、甲香菌酯(jiaxiangjunzhi)、曼德斯宾(mandestrobin)、氯氟醚菌唑、异芬特氟克那唑(ipfentrifluconazole)、苯噻菌酯、美特尔特特拉普罗(metyltetraprole)、烯肟菌酯(enoxastrobin)、丁香菌酯、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、和3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈,其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.04(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:联苯吡菌胺、氯啶菌酯、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、丙硫菌唑、丙环唑、戊唑醇、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、百菌清、氟唑菌酰胺、吡菌苯威、苯并烯氟菌唑、异氟普兰(isoflucypram)、甲香菌酯(jiaxiangjunzhi)、曼德斯宾(mandestrobin)、氯氟醚菌唑、异芬特氟克那唑(ipfentrifluconazole)、苯噻菌酯、美特尔特特拉普罗(metyltetraprole)、烯肟菌酯(enoxastrobin)、丁香菌酯、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、和3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈,其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在根据本发明的优选的组合物中,组分(A)是化合物编号X.01(Z)-2-(5-环丁基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰和美特尔特特拉普罗,其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.02(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰和美特尔特特拉普罗,其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.03(Z)-2-(5-环丙基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰和美特尔特特拉普罗,其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.04(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰和美特尔特特拉普罗,其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在根据本发明的优选的组合物中,组分(A)是化合物编号X.01(Z)-2-(5-环丁基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、丙硫菌唑、嘧菌酯、肟菌酯、唑菌胺酯、和美特尔特特拉普罗(metyltetraprole),其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.02(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、丙硫菌唑、嘧菌酯、肟菌酯、唑菌胺酯、和美特尔特特拉普罗(metyltetraprole),其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.03(Z)-2-(5-环丙基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、丙硫菌唑、嘧菌酯、肟菌酯、唑菌胺酯、和美特尔特特拉普罗(metyltetraprole),其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在根据本发明的另一个优选的组合物中,组分(A)是化合物编号X.04(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯或其盐或互变异构体,并且组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、丙硫菌唑、嘧菌酯、肟菌酯、唑菌胺酯、和美特尔特特拉普罗(metyltetraprole),其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在本发明的一个实施例中,提供了一种协同杀真菌组合物,其包含作为活性成分的组分(A)和(B)的混合物,其中组分(A)是:
(Z)-2-(5-环丁基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.01),
(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.02),
(Z)-2-(5-环丙基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.03),或
(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.04),
或其农艺学上可接受的盐;
并且
组分(B)是选自由以下组成的组的化合物:
环唑醇、苯醚甲环唑、丙硫菌唑、嘧菌酯、肟菌酯、唑菌胺酯、和美特尔特特拉普罗(metyltetraprole)。
优选地,在本发明的实施例中,提供了一种协同杀真菌组合物,其包含作为活性成分的组分(A)和(B)的混合物,其中组分(A)是:
(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.02),或
(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.04);
或其农艺学上可接受的盐;
并且
组分(B)是选自由以下组成的组的化合物:
环唑醇、苯醚甲环唑、丙硫菌唑、嘧菌酯、肟菌酯、唑菌胺酯、和美特尔特特拉普罗(metyltetraprole),其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
更优选地,在本发明的实施例中,提供了一种协同杀真菌组合物,其包含作为活性成分的组分(A)和(B)的混合物,其中组分(A)是:
(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.02),或
(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.04);
或其农艺学上可接受的盐;
并且
组分(B)是嘧菌酯或肟菌酯,其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
甚至更优选地,在本发明的实施例中,提供了一种协同杀真菌组合物,其包含作为活性成分的组分(A)和(B)的混合物,其中组分(A)是:
(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.02),或
(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.04);
或其农艺学上可接受的盐;
并且
组分(B)是嘧菌酯,其中组分(A)与组分(B)的重量比是从10:1至1:10(或者甚至更优选地,7.5:1至1:7.5)。
在本发明的另一个优选实施例中,提供了一种协同杀真菌组合物,其包含作为活性成分的组分(A)和(B)的混合物,其中组分(A)是:
(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.02),或
(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.04);
或其农艺学上可接受的盐;
并且
组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、苯锈啶、丁苯吗啉、咯菌腈、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、灭菌丹、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰、氟唑菌酰羟胺、氯氟醚菌唑、吡啶菌酰胺、美特尔特特拉普罗、N-(2-氟苯基)-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺和[(1S,2S)-1-甲基-2-(邻甲苯基)丙基](2S)-2-[(4-甲氧基-3-丙酰基氧基-吡啶-2-羰基)氨基]丙酸酯(优选地,其中组分(A)与组分(B)的重量比是从100:1至1:100)。
优选地,在本发明的该实施例中,提供了一种协同杀真菌组合物,其包含作为活性成分的组分(A)和(B)的混合物,其中组分(A)是:
(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.02),或
(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.04);
或其农艺学上可接受的盐;
并且
组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、丙硫菌唑、苯锈啶、丁苯吗啉、咯菌腈、嘧菌酯、肟菌酯、唑菌胺酯、代森锰锌、灭菌丹、百菌清、苯并烯氟菌唑、氟唑菌酰羟胺、氯氟醚菌唑、吡啶菌酰胺、美特尔特特拉普罗、N-(2-氟苯基)-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺和[(1S,2S)-1-甲基-2-(邻甲苯基)丙基](2S)-2-[(4-甲氧基-3-丙酰基氧基-吡啶-2-羰基)氨基]丙酸酯,其中组分(A)与组分(B)的重量比是从100:1至1:100(优选地从15:1至1:50,更优选地从10:1至1:10)。
如本文使用的,术语“杀真菌剂”意指控制、改变或预防真菌生长的化合物。术语“杀真菌有效量”意指能够对真菌生长产生影响的这样一种化合物或这样的化合物的组合的量。控制或改变的影响包括所有从自然发育的偏离,如杀死、阻滞等,并且预防包括在植物内或植物上形成屏障或其他防御以预防真菌侵染。
术语“植物”是指植物的所有有形部分,包括种子、幼苗、幼树、根、块茎、茎、秆、叶子和果实。
术语“植物繁殖材料”表示植物的所有生殖部分,例如植物的种子或营养性部分如插条以及块茎。它包括严格意义上的种子、以及根、果实、块茎、球茎、根茎和植物各部分。
如本文使用的,术语“场所”意指植物在其中或其上生长的地方,或栽培植物的种子被播种的地方,或者种子将要被置于土壤中的地方。它包括土壤、种子以及幼苗,连同建立的植被。
贯穿本文件,表述“组合物”代表组分(A)和(B)的不同混合物或组合(包括以上定义的实施例),例如以单一的“掺水即用”的形式,以组合的喷洒混合物(该混合物由这些单一活性成分的单独配制品构成)(例如“桶混制剂”),并且当以一种顺序的方式(即,一个在另一个的适当短的时期之后,例如几小时或几天)施用时,以这些单独活性成分的组合使用。对于实现本发明,施用组分(A)和(B)的顺序并不是重要的。
根据本发明的组合物能有效地对抗引起植物病原性病害的有害微生物(如微生物),特别是对抗植物病原性真菌和细菌。
本发明的组合物可以用于控制由担子菌纲、子嚢菌纲、卵菌纲和/或半知菌纲、芽枝霉纲(Blastocladiomycete)、壶菌纲(Chrytidiomycete)、球囊菌纲(Glomeromycete)和/或粒毛盘菌纲(Mucoromycete)中的广谱的真菌性植物病原体引起的植物病害。
该组合物有效地控制广谱的植物病害,如观赏植物、草皮、蔬菜、田地、谷类、以及水果作物的叶病原体。
这些病原体可以包括:
卵菌纲,包括疫霉病,如由辣椒疫霉菌、致病疫霉菌、大豆疫霉菌、草莓疫莓菌(Phytophthora fragariae)、烟草疫霉菌(Phytophthora nicotianae)、樟疫霉(Phytophthora cinnamomi)、柑橘生疫霉(Phytophthora citricola)、柑橘褐腐疫霉(Phytophthora citrophthora)和马铃薯绯腐病菌(Phytophthora erythroseptica)引起的那些;腐霉病,如由瓜果腐霉菌、强雄腐霉菌(Pythium arrhenomanes)、禾生腐霉菌、畸雌腐霉菌(Pythium irregulare)和终极腐霉菌引起的那些;由霜霉目如大葱霜霉菌(Peronospora destructor)、白菜霜霉菌、葡萄霜霉菌、向日葵霜霉菌、黄瓜霜霉菌、白锈菌(Albugo candida)、水稻霜霉病和莴苣霜霉菌引起的病害;以及其他,如螺壳状丝囊霉、拉布林苏拉佐特雷(Labyrinthula zosterae)、高梁霜指霉(Peronosclerospora sorghi)和禾生指梗霜霉(Sclerospora graminicola)引起的那些;
子囊菌纲,包括斑纹病、斑点病、瘟病或疫病和/或腐病,例如由如下引起的那些:格孢菌目如大蒜白斑病菌(Stemphylium solani)、台南水仙壳多孢(Stagonosporatainanensis)、油橄榄环梗孢菌、玉米大斑病菌(Setosphaeria turcica)、番茄须壳孢(Pyrenochaeta lycoperisici)、枯叶格孢腔菌、实腐茎点霉(Phoma destructiva)、麦叶暗球腔菌(Phaeosphaeria herpotrichoides)、高曼尼棕隐球菌(Phaeocryptocusgaeumannii)、禾生蛇孢腔菌(Ophiosphaerella graminicola)、小麦全蚀病(Ophiobolusgraminis)、十字花科小球腔菌(Leptosphaeria maculans)、软腐病菌(Hendersoniacreberrima)、壳针孢叶枯病菌(Helminthosporium triticirepentis)、玉米大斑病菌(Setosphaeria turcica)、大豆内脐蠕孢(Drechslera glycines)、西瓜蔓枯病菌(Didymella bryoniae)、油橄榄孔雀斑病菌(Cycloconium oleagineum)、多主棒孢菌(Corynespora cassiicola)、禾旋孢腔菌、火龙果黑斑病菌(Bipolaris cactivora)、苹果黑星病菌、圆核腔菌、燕麦草核腔菌(Pyrenophora tritici-repentis)、互隔链格孢菌、芸苔链格孢菌(Alternaria brassicicola)、茄链格孢菌和西红柿链格孢菌(Alternariatomatophila);煤炱目(Capnodiales)如小麦壳针孢、颖枯壳针孢、大豆壳针孢(Septoriaglycines)、落花生尾孢菌(Cercospora arachidicola)、大豆灰斑病菌、玉米灰斑病菌、荠白斑病菌(Cercosporella capsellae)以及麦叶白霉(Cercosporella herpotrichoides)、桃疮痂病菌(Cladosporium carpophilum)、散生枝孢(Cladosporium effusum)、褐孢霉(Passalora fulva)、尖孢枝孢(Cladosporium oxysporum)、松针座囊菌(Dothistromaseptosporum)、葡萄褐斑病菌(Isariopsis clavispora)、香蕉黑条叶斑病菌、禾生球腔菌(Mycosphaerella graminicola)、散梗菌绒孢菌(Mycovellosiella koepkeii)、甘薯暗拟棒束梗霉(Phaeoisariopsis bataticola)、葡萄褐斑病菌(Pseudocercospora vitis)、小麦基腐病菌、甜菜叶斑病菌、柱隔孢叶斑病菌(Ramularia collo-cygni);大角间座壳目如小麦全蚀病菌、稻瘟病菌(Magnaporthe grisea)、稻梨孢;间座壳目如榛子东部枯萎病菌、阿皮奥诺莫尼亚厄拉班达(Apiognomonia errabunda)、梧桐壳囊孢(Cytospora platani)、大豆北方茎溃疡病菌、毁灭性座盘孢(Discula destructiva)、草莓日规壳菌(Gnomoniafructicola)、葡萄苦腐病菌、核桃黑盘壳菌(Melanconium juglandinum)、葡萄生拟茎点菌(Phomopsis viticola)、胡桃溃疡病菌(Sirococcus clavigignenti-juglandacearum)、干孢盾壳椿启介菌(Tubakia dryina)、地卡佩拉属物种(Dicarpella spp.)、苹果树腐烂病菌(Valsa ceratosperma);以及其他,如阿提诺赛睿姆格拉密尼斯(Actinothyriumgraminis)、豌豆壳二孢、黄曲霉、烟曲霉菌、构巢曲霉、番木瓜座糙孢菌、叶斑病菌(Blumeriella jaapii)、假丝酵母属物种、煤炱病菌(Capnodium ramosum)、瑟发罗所卡斯属物种(Cephaloascus spp.)、麦类条斑病菌(Cephalosporium gramineum)、奇异长喙壳(Ceratocystis paradoxa)、毛壳菌属物种、拟白膜盘菌(Hymenoscyphus pseudoalbidus)、球孢子菌属物种、李属柱孢霉(Cylindrosporium padi)、双壳菌(Diplocarpon malae)、芸苔偏盘菌(Drepanopeziza campestris)、痂囊腔菌(Elsinoe ampelina)、黑附球菌、表皮癣菌属物种、葡萄顶枯病、白地霉、禾谷绒座壳(Gibellina cerealis)、高粱胶尾孢(Gloeocercospora sorghi)、煤烟病菌(Gloeodes pomigena)、宿根盘长孢(Gloeosporiumperennans);毒麦内生真菌(Gloeotinia temulenta)、皮生隔孢壳(Griphospaeriacorticola)、利尼球梗孢(Kabatiella lini)、小孢粘束孢(Leptographium microsporum)、厚囊小光腔菌(Leptosphaerulinia crassiasca)、扰乱散斑壳(Lophodermiumseditiosum)、禾谷盘二孢菌(Marssonina graminicola)、雪霉叶枯菌(Microdochiumnivale)、美澳型核果褐腐病菌(Monilinia fructicola)、稻云形病(Monographellaalbescens)、甜瓜黑点根腐病菌(Monosporascus cannonballus)、丝环盘菌属物种(Naemacyclus spp.)、新榆枯萎病菌(Ophiostoma novo-ulmi)、巴西副球孢子菌(Paracoccidioides brasiliensis)、扩展青霉(Penicillium expansum)、杜鹃盘多毛孢霉(Pestalotia rhododendri)、霉样真霉属物种(Petriellidium spp.)、无柄盘菌属物种(Pezicula spp.)、大豆茎褐腐病菌(Phialophora gregata)、仁果黑痣菌(Phyllachorapomigena)、杂食动物瘤梗孢(Phymatotrichum omnivora)、隐秘囊孢菌(Physalosporaabdita)、烟草囊孢壳(Plectosporium tabacinum)、马铃薯皮斑病菌(Polyscytalumpustulans)、苜蓿假盘菌(Pseudopeziza medicaginis)、芸薹埋核盘菌(Pyrenopezizabrassicae)、高粱座枝孢(Ramulispora sorghi)、花旗松藩叶病菌(Rhabdoclinepseudotsugaae)、大麦云纹病菌(Rhynchosporium secalis)、稻帚枝杆孢(Sacrocladiumoryzae)、足放线病菌属物种(Scedosporium spp.)、仁果裂盾菌(Schizothyrium pomi)、核盘菌(Sclerotinia sclerotiorum)、小核盘菌(Sclerotinia minor);小核菌属物种(Sclerotium spp.)、雪腐病核瑚菌(Typhula ishikariensis)、玛丽盘双端毛孢(Seimatosporium mariae)、柏树细弯孢壳菌(Lepteutypa cupressi)、紫白斑菌(Septocyta ruborum)、鳄梨疮痂病菌(Sphaceloma perseae)、苜蓿枝梗边裂壳(Sporonemaphacidioides)、千年枣眼点病菌(Stigmina palmivora)、塔佩西亚伦迪(Tapesiayallundae)、梨外囊菌(Taphrina bullata)、棉花黑根腐病菌(Thielviopsis basicola)、特里克斯托利亚弗鲁提吉纳(Trichoseptoria fructigena)、蝇粪病菌(Zygophialajamaicensis);白粉病,例如由白粉菌目如小麦白粉病菌、蓼白粉病菌、葡萄钩丝壳、黄瓜白粉病菌(Sphaerotheca fuligena)、白叉丝单囊壳、斑点白粉菌(Podospaera macularis)、二孢白粉菌(Golovinomyces cichoracearum)、鞑靼内丝白粉菌(Leveillula taurica)、扩散叉丝壳、棉花拟粉孢(Oidiopsis gossypii)、榛球针壳(Phyllactinia guttata)以及落花生粉孢霉菌(Oidium arachidis)引起的那些;霉,例如由葡萄座腔菌如小穴壳菌(Dothiorella aromatica)、连续色二孢(Diplodia seriata)、比德瓦里球座菌(Guignardia bidwellii)、灰葡萄孢菌(Botrytis cinerea)、大葱孢盘菌(Botryotiniaallii)、蚕豆孢盘菌(Botryotinia fabae)、扁桃壳梭菌(Fusicoccum amygdali)、龙眼焦腐病菌(Lasiodiplodia theobromae)、茶生大茎点霉(Macrophoma theicola)、菜豆壳球孢菌、葫芦科叶点霉(Phyllosticta cucurbitacearum)引起的那些;炭疽病,例如由小丛壳(Glommerelales)如盘长孢状刺盘孢、瓜类炭疽菌(Colletotrichum lagenarium)、棉花炭疽病菌、围小丛壳、以及禾生炭疽菌引起的那些;以及枯萎病或疫病,例如由肉座菌目如笔直顶孢霉、紫麦角菌、黄色镰刀菌、禾谷镰刀菌、大豆猝死综合症病菌(Fusariumvirguliforme)、尖孢镰刀菌、胶孢镰刀菌、古巴尖孢镰孢(Fusarium oxysporumf.sp.cubense)、雪腐格氏霉(Gerlachia nivale)、藤仓赤霉、玉米赤霉、胶枝霉属、疣孢漆斑菌、拉姆拉雷丛赤壳菌(Nectria ramulariae)、绿色木霉、粉红聚端孢菌和鳄梨根腐病原菌(Verticillium theobromae)引起的那些;
担子菌纲,包括黑粉病例如由黑粉菌目如稻曲病菌(Ustilaginoidea virens)、大麦散黑穗病菌(Ustilago nuda)、小麦散黑穗菌(Ustilago tritici)、玉米黑粉菌(Ustilago zeae)引起的那些,锈病例如由柄锈菌如无花果蜡锈菌(Cerotelium fici)、云杉帚锈病菌(Chrysomyxa arctostaphyli)、番薯鞘锈菌(Coleosporium ipomoeae)、咖啡驼孢锈菌(Hemileia vastatrix)、落花生柄锈菌(Puccinia arachidis)、西南棉花柄锈菌(Puccinia cacabata)、禾柄锈菌(Puccinia graminis)、隐匿柄锈菌(Pucciniarecondita)、高粱柄锈菌(Puccinia sorghi)、大麦柄锈菌(Puccinia hordei)、大麦条形柄锈菌(Puccinia striiformis f.sp.Hordei)、小麦条形柄锈菌(Puccinia striiformisf.sp.Secalis)、榛膨痂锈菌(Pucciniastrum coryli)引起的那些;或锈菌目如松疱锈病菌(Cronartium ribicola)、植物受桧胶锈菌(Gymnosporangium juniperi-viginianae)、杨树叶锈病菌(Melampsora medusae)、豆薯层锈菌(Phakopsora pachyrhizi)、短尖多胞锈菌(Phragmidium mucronatum)、白蔹壳锈菌(Physopella ampelosidis)、变色疣双胞锈菌(Tranzschelia discolor)以及蚕豆单孢锈菌(Uromyces viciae-fabae)引起的那些;以及其他腐病和病害,如由隐球菌属物种、茶饼病菌(Exobasidium vexans)、因诺德玛微伞皮(Marasmiellus inoderma)、小菇属物种、丝黑穗病菌(Sphacelotheca reiliana)、雪腐病核瑚菌(Typhula ishikariensis)、冰草条黑粉菌(Urocystis agropyri)、花枯锁霉(Itersonilia perplexans)、因微瑟姆伏革菌(Corticium invisum)、地衣状伏革菌(Laetisaria fuciformis)、旋卷似串担革菌(Waitea circinata)、立枯丝核菌、瓜亡革菌(Thanetephorus cucurmeris)、大丽花叶黑粉菌(Entyloma dahliae)、小孢叶黑粉菌(Entylomella microspora)、沼湿草尾孢黑粉菌(Neovossia moliniae)和小麦网腥黑粉菌(Tilletia caries)引起的那些;
芽枝霉纲,如玉蜀黍节壶菌(Physoderma maydis);
毛霉菌纲,如瓜笄霉菌(Choanephora cucurbitarum);毛霉属物种;少根根霉;
连同由与以上列出的那些紧密相关的其他物种和属引起的病害。
除了它们的杀真菌活性之外,这些组合物还可以具有针对细菌如梨火疫病菌、软腐欧文氏菌(Erwinia caratovora)、野油菜黄单胞菌、丁香假单胞菌、马铃薯疮痂病菌(Strptomyces scabies)和其他相关物种连同某些原生动物的活性。
根据本发明的组合物尤其能有效地对抗属于以下类别的植物病原性真菌:子嚢菌纲(例如:黑星菌属、叉丝单嚢壳属、白粉属、丛梗孢属、球腔菌属、钩丝壳属);担子菌纲(例如Hemileia属、丝核菌属、层锈菌属、柄锈菌属、黑粉菌属、腥黑粉菌属);半知菌类(也称作半知菌纲、例如葡萄孢属、长蠕孢属、喙孢属、镰刀菌属、壳针孢属、尾孢属、链格孢属、梨孢属和假小尾孢属);卵菌纲(例如疫霉属、霜霉属、假霜霉属、白锈属、盘梗霉属、腐霉属、假指梗霉属、单轴霉属)。
根据本发明的组合物可以用于其中的有用植物作物包括多年生和一年生作物,如浆果植物,例如黑莓、蓝莓、蔓越莓、树莓以及草莓;谷物,例如大麦、玉米(maize,corn)、粟、燕麦、水稻、黑麦、高粱、黑小麦以及小麦;纤维植物,例如棉花、亚麻、大麻、黄麻以及剑麻;大田作物,例如糖甜菜和饲料甜菜、咖啡豆、啤酒花、芥菜、油菜(卡诺拉)、罂粟、甘蔗、向日葵、茶以及烟草;果树,例如苹果、杏、鳄梨、香蕉、樱桃、柑橘、油桃、桃、梨以及李子;草,例如百慕达草、蓝草、本特草、蜈蚣草、牛毛草、黑麦草、圣奥古斯丁草以及结缕草;药草,如罗勒、琉璃苣、细香葱、胡荽、薰衣草、独活草、薄荷、牛至、荷兰芹、迷迭香、鼠尾草以及百里香;豆类,例如菜豆、小扁豆、豌豆以及大豆;坚果,例如杏仁、腰果、落花生、榛子、花生、山核桃、开心果以及核桃;棕榈植物,例如油棕榈;观赏植物,例如花、灌木以及树;其他树木,例如可可树、椰子树、橄榄树以及橡胶树;蔬菜,例如芦笋、茄子、西兰花、卷心菜、胡萝卜、黄瓜、大蒜、莴苣、西葫芦、甜瓜、秋葵、洋葱、胡椒、马铃薯、南瓜、大黄、菠菜以及番茄;和葡萄藤,例如葡萄。
作物应当被理解为是天然存在的、通过常规的育种方法获得或通过基因工程获得的那些。它们包括含有所谓的输出型(output)性状(例如改善的储存稳定性、更高的营养价值以及改善的风味)的作物。
作物应被理解为还包括已经被赋予对除草剂(像溴草腈)或多种类别的除草剂(如ALS-、EPSPS-、GS-、HPPD-和PPO-抑制剂)的耐受性的那些作物。通过常规的育种方法已经被赋予了对咪唑啉酮(例如,甲氧咪草烟)的耐受性的作物的实例是夏季卡诺拉。通过遗传工程方法而被赋予了对除草剂的耐受性的作物的实例包括例如草甘膦和草铵膦抗性玉米品种,这些玉米品种以商标名和是可商购的。
作物还应被理解为天然地是或已经赋予对害虫的抗性的那些作物。这包括通过使用重组DNA技术转化从而例如能够合成一种或多种选择性作用毒素的植物,这些毒素是如从例如产毒素的细菌已知的。可以被表达的毒素的实例包括δ-内毒素,营养期杀虫蛋白(Vip),细菌定殖线虫的杀虫蛋白,以及由蝎子、蛛形纲动物、黄蜂和真菌产生的毒素。
已经被修饰为表达苏云金芽孢杆菌毒素的作物的实例是Bt maize(先正达种子公司(Syngenta Seeds))。包括编码杀虫抗性并且由此表达多于一种毒素的多于一种基因的作物的实例是(先正达种子公司)。作物或其种子材料还可以是对多种类型的有害生物具有抗性(当通过遗传修饰产生时的所谓的叠加转基因事件)。例如,植物可以具有表达杀虫蛋白同时耐受除草剂的能力,例如Herculex(陶氏益农公司(Dow AgroSciences),先锋良种国际公司(Pioneer Hi-BredInternational))。
具有式(I)的化合物(包括化合物X.01至X.04中的任一种)或包含具有式(I)的化合物的根据本发明的杀真菌组合物可用于控制或预防大豆植物上的植物病原性病害、尤其是植物病原性真菌(如豆薯层锈菌)。
特别地,表达毒素例如杀昆虫蛋白如δ-内毒素(例如Cry1Ac(Cry1Ac Bt蛋白))的转基因大豆植物。因此,这可以包括转基因大豆植物,其包含事件MON87701(参见美国专利号8,049,071以及相关申请和专利,以及WO 2014/170327 A1(例如参见关于Intacta RR2PROTM大豆的段落[008]))、事件MON87751(美国专利申请公开号2014/0373191)或事件DAS-81419(美国专利号8632978以及相关申请和专利)。
其他转基因大豆植物可以包含事件SYHT0H2-HPPD耐受性(美国专利申请公开号2014/0201860以及相关申请和专利)、事件MON89788-草甘膦耐受性(美国专利号7,632,985以及相关申请和专利)、事件MON87708-麦草畏耐受性(美国专利申请公开号US 2011/0067134以及相关申请和专利)、事件DP-356043-5-草甘膦以及ALS耐受性(美国专利申请公开号US 2010/0184079以及相关申请和专利)、事件A2704-12-草铵膦耐受性(美国专利申请公开号US 2008/0320616以及相关申请和专利)、事件DP-305423-1-ALS耐受性(美国专利申请公开号US 2008/0312082以及相关申请和专利)、事件A5547-127-草铵膦耐受性(美国专利申请公开号US 2008/0196127以及相关申请和专利)、事件DAS-40278-9-对2,4-二氯苯氧基乙酸和芳氧基苯氧基丙酸酯的耐受性(参见WO 2011/022469、WO 2011/022470、WO 2011/022471、以及相关申请和专利)、事件127-ALS耐受性(WO 2010/080829以及相关申请和专利)、事件GTS 40-3-2-草甘膦耐受性、事件DAS-68416-4-2,4-二氯苯氧基乙酸以及草铵膦耐受性、事件FG72-草甘膦和异噁唑草酮耐受性、事件BPS-CV127-9-ALS耐受性以及GU262-草铵膦耐受性或事件SYHT04R-HPPD耐受性。
具有式(I)的化合物(包括化合物X.01至X.04中的任一种)或包含具有式(I)的化合物的根据本发明的杀真菌组合物可用于控制或预防大豆植物上的植物病原性病害、尤其是植物病原性真菌(如豆薯层锈菌)。特别地,在科学文献中存在已知的某些优良大豆植物品种,其中赋予对特定豆薯层锈菌的一定程度免疫力或抗性的R基因堆叠已在植物基因组中渗入,参见例如:“Fighting Asian Soybean Rust[与亚洲大豆锈病战斗]”,LangenbachC等人,Front Plant Science[植物科学前沿]7(797)2016)。
优良植物是来自优良品系的任何植物,因此优良植物是来自优良品种的代表性植物。农民或大豆育种者可商购的优良大豆品种的非限制性实例包括:AG00802、A0868、AG0902、A1923、AG2403、A2824、A3704、A4324、A5404、AG5903、AG6202、AG0934;AG1435;AG2031;AG2035;AG2433;AG2733;AG2933;AG3334;AG3832;AG4135;AG4632;AG4934;AG5831;AG6534;和AG7231(阿斯格罗种子公司(Asgrow Seeds),德梅因(Des Moines),爱荷华州,美国);BPR 0144RR、BPR 4077NRR和BPR 4390NRR(生物植物研究所(Bio Plant Research),营点(Camp Point),伊利诺伊州,美国);DKB17-51和DKB37-51(迪卡白遗传公司(DeKalbGenetics),迪卡尔布(DeKalb),伊利诺伊州,美国);DP 4546RR、和DP 7870RR(三角洲和松树陆地公司(Delta&Pine Land Company),卢博克市(Lubbock),德克萨斯州,美国);JG03R501、JG 32R606C ADD和JG 55R503C(JGL有限公司(JGL Inc.),格林卡斯尔(Greencastle),印第安纳州,美国);NKS 13-K2(先正达种子公司NK部门(NK Division ofSyngenta Seeds),黄金谷(Golden Valley),明尼苏达洲,美国);90M01、91M30、92M33、93M11、94M30、95M30、97B52、P008T22R2;P16T17R2;P22T69R;P25T51R;P34T07R2;P35T58R;P39T67R;P47T36R;P46T21R;和P56T03R2(先锋良种国际有限公司(Pioneer Hi-BredInternational),庄士敦(Johnston),爱荷华州,美国);SG4771NRR和SG5161NRR/STS(大豆遗传学有限责任公司(Soygenetics,LLC,),拉斐特(Lafayette),印第安纳州,美国);S00-K5、S11-L2、S28-Y2、S43-B1、S53-A1、S76-L9、S78-G6、S0009-M2;S007-Y4;S04-D3;S14-A6;S20-T6;S21-M7;S26-P3;S28-N6;S30-V6;S35-C3;S36-Y6;S39-C4;S47-K5;S48-D9;S52-Y2;S58-Z4;S67-R6;S73-S8;和S78-G6(先正达种子公司,亨德森市(Henderson),肯塔基州,美国);Richer(北极星种业有限责任公司(Northstar Seed Ltd.),亚伯达省(Alberta),加拿大);14RD62(斯汀种子公司(Stine Seed Co.),爱荷华州,美国);或Armor 4744(阿莫尔种子有限责任公司(Armor Seed,LLC),阿拉斯加州,美国)。
因此,在另一个优选的实施例中,使用包含具有式(I)的化合物(包括化合物X.01至X.04中的任一种)的根据本发明的杀真菌组合物控制优良大豆植物品种上的豆薯层锈菌(包括其杀真菌抗性菌株,如下所述),其中赋予对特定豆薯层锈菌的一定程度免疫力或抗性的R基因堆叠已在植物基因组中渗入。从所述用途可以预期产生许多益处,例如改善的生物活性,有利或更宽的活性谱(包括豆薯层锈菌的敏感和抗性菌株),增加的安全性,改善的作物耐受性,协同相互作用或增强特性,改善的起效或更长持续残留活性,减少有效控制植物病原菌(豆薯层锈菌)所需的化合物和组合物的施用次数和/或降低其施用率,从而实现有益的抗性-管理实践,降低的环境影响和减少的操作员暴露。
在某些情况下,当用于控制或预防大豆植物(特别是如上所述的任何转基因大豆植物)上的植物病原性病害、尤其是植物病原性真菌(如豆薯层锈菌)时,包含具有式(I)的化合物的根据本发明的杀真菌组合物可显示活性成分之间的协同相互作用。
包含具有式(I)的化合物(包括化合物X.01至X.04中的任一种)的根据本发明的杀真菌组合物可以用于控制或预防大豆植物上的植物病原性病害尤其是植物病原性真菌(特别是豆薯层锈菌)。
另外,迄今为止,在包含具有式(I)的化合物(包括化合物X.01至X.04中的任一种)的根据本发明的杀真菌组合物与用于控制豆薯层锈菌的当前杀真菌溶液之间未观察到交叉抗性。
实际上,在科学文献中已经报道了豆薯层锈菌的杀真菌抗性菌株,其中观察到对一种或多种杀真菌剂具有抗性的菌株,该一种或多种杀真菌剂来自以下杀真菌作用模式类别的至少每一种:甾醇去甲基化抑制剂(DMI)、醌外抑制剂(QoI)和琥珀酸脱氢酶抑制剂(SDHI)。参见例如:“Sensitivity of Phakopsora pachyrhizi towards quinone-outside-inhibitors and demethylation-inhibitors,and corresponding resistancemechanisms[豆薯层锈菌对苯醌外部抑制剂和去甲基化抑制剂的敏感性,以及相应的耐药机制].”Schmitz HK等人,Pest Manag Sci[有害生物管理学](2014)70:378-388;“Firstdetection of a SDH variant with reduced SDHI sensitivity in Phakopsorapachyrhizi[在豆薯层锈菌中首次检测到具有降低的SDHI敏感性的SDH变体]”K等人,J Plant Dis Prot[植物病害保护杂志](2018)125:21-2;“Competitive fitness ofPhakopsora pachyrhizi isolates with mutations in the CYP51 and CYTB genes[具有CYP51和CYTB基因突变的豆薯层锈菌分离株的竞争适应性].”Klosowski AC等人,Phytopathology[植物病理学](2016)106:1278-1284;“Detectionof the F129L mutationin the cytochrome b gene in Phakopsora pachyrhizi[豆薯层锈菌细胞色素b基因中F129L突变的检测].”Klosowski AC等人,Pest Manag Sci[有害生物管理学](2016)72:1211-1215。
因此,在优选的实施例中,包含具有式(I)的化合物(包括化合物X.01至X.04中的任一种)的根据本发明的杀真菌组合物用于控制豆薯层锈菌,其对来自以下杀真菌MoA类别的任一种的一种或多种杀真菌剂具有抗性:甾醇去甲基化抑制剂(DMI)、醌外抑制剂(QoI)和琥珀酸脱氢酶抑制剂(SDHI)。
可以如以下方案所示制备构成本发明的组分A的化合物,其中R1、R2、R3和R4如对式(I)所定义。
具有式(I)的化合物(其中R1、R2、R3和R4如上所定义)可以经由任选地在金属盐(如LiCl或ZnCl2)和合适的金属催化剂络合物(如氯(2-二环己基膦基-2′,4′,6′-三异丙基-1,1′-联苯基)[2-(2′-氨基-1,1′-联苯基)]钯(II))的存在下,在有机溶剂(如四氢呋喃或1,4-二噁烷)中,在20℃-150℃之间的温度下,具有式(II)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义并且R11是卤化物或拟卤化物如氯、溴、碘、-OSO2CF3或-OSO2(CF2)3CF3)与具有式(III)的化合物(其中R4如对于具有式(I)的化合物所定义,并且M是类金属物质或拟类金属物质(例如M包括但不限于MgCl、ZnCl或B(OH)2))之间的交叉偶联转换获得。对于相关实例,参见:Journal of Organic Chemistry[有机化学杂志],2010,75,6677-6680,Journal of the American Chemical Society[美国化学学会杂志],2009,131,7532-7533,European Journal of Medicinal Chemistry[欧洲药物化学杂志],2018,147,238-252,以及由Norio Miyaura和S.L.Buchwald编辑的“Cross-Coupling Reactions:APractical Guide(Topics in Current Chemistry)[交叉偶联反应:实用指南(当代化学专题)](Springer[施普林格出版社]版本)”,或者由Armin de Meijere和Diederich编辑的“Metal-Catalyzed Cross-Coupling Reactions[金属催化的交叉偶联反应](WILEY-VCH[威利-VCH出版社]版本)”。
这在方案1中示出。
方案1
可替代地,具有式(I)的化合物可以通过使具有式(IV)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义,并且R12是部分不饱和的、任选地取代的C3-C7环烯基)经由还原方法(如使用氢源在催化剂络合物如钯碳存在下,在有机溶剂如甲醇、四氢呋喃或乙酸乙酯中,在0℃-150℃之间的温度下进行氢化)进行反应而获得。对于相关实例,参见:ACSMedicinal Chemistry Letters[ACS医药化学通讯],2016,7,508-51。Shigeo Nishimura的‘Handbook of Heterogeneous Catalytic Hydrogenation for Organic Synthesis[有机合成多相催化氢化手册]’(由Wiley-VCH[威利出版社]出版)或Johannes de Vries和Cornelis Elsevier编辑的‘The Handbook of Homogeneous Hydrogenation[均相氢化手册]’(由Wiley-VCH[威利-VCH出版社]出版)。这在方案2中示出。
方案2
具有式(IV)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义,并且R12是部分饱和的并且任选地取代的C3-C7环烯基)可以使用合适的催化剂络合物如钯(四(三苯基膦)),在溶剂如1,4-二噁烷、二甲基甲酰胺或四氢呋喃中,在0℃-150℃之间的温度下,以及任选地在碱(例如磷酸钾)的存在下,经由具有式(II)的化合物(其中R11是卤化物或拟卤化物如氯、溴、碘、-OSO2CF3或-OSO2(CF2)3CF3)与具有式(V)的化合物(其中M表示类金属或拟类金属物质(例如M包括但不限于B(OH)2、BPin、SnBu3)或氢)之间的交叉偶联反应获得。对于相关实例,参见:ACS Medicinal Chemistry Letters[ACS医药化学通讯],2016,7,508-513和由Norio Miyaura和S.L.Buchwald编辑的“Cross-Coupling Reactions:A PracticalGuide(Topics in Current Chemistry)[交叉偶联反应:实用指南(当代化学专题)](Springer[施普林格出版社]版本)”,或者由Armin de Meijere和Diederich编辑的“Metal-Catalyzed Cross-Coupling Reactions[金属催化的交叉偶联反应](WILEY-VCH[威利-VCH出版社]版本)”。这在方案3中示出。
方案3
具有式(II)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义并且R11是卤化物或拟卤化物如氯、溴、碘、-OSO2CF3或-OSO2(CF2)3CF3)可以由具有式(VI)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义,R11如上所定义并且R13是H或C1-C4烷基)经由以下方式获得:用合适的碱如甲醇钠和甲酰化剂如甲酸甲酯任选地在合适的溶剂(例如四氢呋喃)中进行处理以生成具有式(VIa)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义,R11如上所定义并且R14是H或甲基),接着任选地在碱如K2CO3的存在下用试剂如硫酸二甲酯进行甲基化。对于相关实例,参见:Journal of Agricultural and FoodChemistry[农业与食品化学杂志],2007,55,5697-5700,Molecules[分子],2010,15,9024-9034和Organic Process Research and Development[有机工艺研究与开发],2015,19,639-645。这在方案4中示出。
方案4
具有式(VI)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义,R11如上所定义并且R13是H或C1-C4烷基)可以由具有式(VII)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义并且R11如上所定义)通过在有机溶剂如二甲基甲酰胺或N-甲基吡咯烷酮中用碱如K2CO3和具有式(VIII)的烷基化剂(其中R13是H或C1-C4烷基)处理来获得。具有式(VII)的化合物是可商购的或者由可商购的化合物通过如在March’s Advanced OrganicChemistry[March高等有机化学],Smith和March,第6版,Wiley[威利出版社],2007中所描述的标准官能团转换容易地制备。这在方案5中示出。
方案5
具有式(I)的化合物(其中R1、R2、R3和R4如对于具有式(I)的化合物所定义)还可以由具有式(IX)的化合物(其中R1、R2、R3和R4如对于具有式(I)的化合物所定义并且R13是H或C1-C4烷基)通过以下方式获得:用碱如甲醇钠和甲酰化剂如甲酸甲酯处理以生成具有式(X)的化合物(其中R1、R2、R3和R4如对于具有式(I)的化合物所定义并且R14是H或甲基),接着在碱如K2CO3的存在下用试剂如硫酸二甲酯进行甲基化。对于相关实例,参见:Journal ofAgricultural and Food Chemistry[农业与食品化学杂志],2007,55,5697-5700,Molecules[分子],2010,15,9024-9034和Organic Process Research and Development[有机工艺研究与开发],2015,19,639-645。
这在方案6中示出。
方案6
具有式(IX)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义并且R4是任选地取代的环丙基)可以由具有式(XI)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义并且R15表示任选地取代的烯基)通过用二碘甲烷,用有机锌试剂如二乙基锌,任选地在酸源如三氟乙酸的存在下,并且在有机溶剂如二氯甲烷中处理来制备。对于相关实例,参见:Organic Reactions[有机反应],2001,58,1。这在方案7中示出。
方案7
具有式(XI)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义,R15如上所定义并且R13是H或C1-C4烷基)可以由具有式(XII)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义并且R15如上所定义)通过在有机溶剂如二甲基甲酰胺或N-甲基吡咯烷酮中用碱如K2CO3和具有式(VIII)的烷基化剂(其中R13是H或C1-C4烷基)处理来获得。这在方案8中示出。对于相关实例,参见:European Journal of Organic Chemistry[欧洲有机化学杂志],2015,2197-2204。具有式(VIII)的化合物是可商购的或者由可商购的化合物通过如在March’s Advanced Organic Chemistry[March高等有机化学],Smith和March,第6版,Wiley[威利出版社],2007中所描述的标准官能团转换容易地制备。
方案8
具有式(XII)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义并且R15如上所定义)可以使用合适的催化剂络合物如钯(四(三苯基膦)),在合适的溶剂如二噁烷、二甲基甲酰胺或四氢呋喃中,在0℃-150℃之间的温度下,以及任选地碱如磷酸钾或碳酸钾,经由具有式(VII)的化合物(其中R1、R2和R3如对于具有式(I)的化合物所定义并且R11是卤化物或拟卤化物如氯、溴、碘、-OSO2CF3或-OSO2(CF2)3CF3)与具有式(XIII)的化合物(其中R15如上所定义并且M表示类金属物质或拟类金属物质(例如M包括但不限于B(OH)2、BPin、SnBu3)或氢)之间的偶联转换制备。对于相关实例,参见:Journal of Medicinal Chemistry[医药化学杂志],2015,58,9258-9272和Journal of Medicinal Chemistry[医药化学杂志],2014,57,1252-1275。这在方案9中示出。
方案9
先前方案中所描述的官能团相互转化是本领域技术人员已知的。可以在以下中找到反应条件的广泛列表:由A.R.Katritzky,O.Meth-Cohn和C.W.Rees.编辑的Comprehensive Organic Functional Group Transformations[综合有机官能团转换],Pergamon Press[培格曼出版社](爱思唯尔科学有限公司(Elsevier Science Ltd.)),纽约柏油村(Tarrytown,NY.)1995;或由Richard C.Larock编辑的Comprehensive OrganicTransformations:A Guide to Functional Group Preparations[综合有机转换:官能团制备指南],Wiley-VCH[威利-VCH出版社],纽约(New York)1999。
如果合成产生异构体的混合物,则分离通常不一定是必需的,因为在某些情况下,各个异构体可以在后处理用于使用期间或在施用期间(例如在光、酸或碱的作用下)相互转化。此种转化也可以在使用后发生,例如在处理过的植物中在植物处理中或在要控制的有害真菌中。
可以将包括所有上述披露的实施例和其优选实例的本发明的组合物与一种或多种另外的杀有害生物剂混合,这些杀有害生物剂包括另外的杀真菌剂、杀昆虫剂、杀线虫剂、杀细菌剂、杀螨剂、生长调节剂、化学不育剂、化学信息素、驱虫剂、引诱剂、信息素、取食刺激剂或其他生物活性化合物以形成给出更广谱农业保护的多组分杀有害生物剂。
此类农业保护剂的实例与本发明的组合物可以配制为:
杀真菌剂如土菌灵、氟啶胺、苯霜灵、苯霜灵-M(精苯霜灵)、呋霜灵、甲霜灵、甲霜灵-M(精甲霜灵)、多地辛、N'-(2,5-二甲基-4-苯氧基-苯基)-N-乙基-N-甲基-甲脒、N'-[4-(4,5-二氯-噻唑-2-基氧基)-2,5-二甲基-苯基]-N-乙基-N-甲基-甲脒、N'-[4-[[3-[(4-氯苯基)甲基]-1,2,4-噻二唑-5-基]氧基]-2,5-二甲基-苯基]-N-乙基-N-甲基-甲脒、乙菌定、3’-氯-2-甲氧基-N-[(3RS)-四氢-2-氧代呋喃-3-基]乙酰-2',6'-二甲基苯胺(抑霉胺(clozylacon))、嘧菌环胺、嘧菌胺、嘧霉胺、二噻农、金色制霉素、杀稻瘟菌素-S、联苯、地茂散、氯硝铵、苯并烯氟菌唑、氟唑菌酰羟胺、六氯苯、五氯硝基苯、四氯硝基苯(TCNB)、甲基立枯磷、苯菌酮、2,6-二氯-N-(4-三氟甲基苄基)-苯甲酰胺、氟吡菌胺(fluopicolide或flupicolide)、硫氰苯甲酰胺(tioxymid)、磺菌胺、苯菌灵、多菌灵、多菌灵盐酸盐、氯芬唑(chlorfenazole)、麦穗宁、噻苯咪唑、甲基硫菌灵、苯噻菌胺、灭瘟唑、噻菌灵、阿拉酸式苯、百杀辛(bethoxazin)、甲氧苯唳菌(pyriofenone)(IKF-309)、阿拉酸式苯-S-甲基、吡菌苯威(KIF-7767)、丁胺、3-碘-2-丙炔基正丁基氨基甲酸酯(IPBC)、碘代丙炔基丁基氨基甲酸酯(iodocarb)(异丙基丁基氨基甲酸酯)、异丙基丁基氨基甲酸酯(碘代丙炔基丁基氨基甲酸酯)、四唑吡氨酯、聚氨基甲酸酯、霜霉威、三氟甲氧威(tolprocarb)、3-(二氟甲基)-N-(7-氟-1,1,3,3-四甲基-茚满-4-基)-1-甲基-吡唑-4-甲酰胺、双氯氰菌胺、N-[(5-氯-2-异丙基-苯基)甲基]-N-环丙基-3-(二氟甲基)-5-氟-1-甲基-吡唑-4-甲酰胺、N-环丙基-3-(二氟甲基)-5-氟-N-[(2-异丙基苯基)甲基]-1-甲基-吡唑-4-甲酰胺、环丙酰菌胺、百菌清、氟吗啉、喹啉铜(oxine-copper)、霜脲氰、氰烯菌酯、氰霜唑、氟噻唑菌腈、噻菌腈、乙菌利、异菌脲、腐霉利、农利灵、磺酸丁嘧啶、邻敌螨消、硝戊酯、消螨通、敌螨普、消螨多、二苯胺、氯瘟磷、2,6-二甲基-[1,4]二噻英并[2,3-c:5,6-c']二吡咯-1,3,5,7(2H,6H)-四酮、氧化福美双、代森硫、福美铁、代森锰锌、代森锰、威百亩(metam)、代森联(metiram或polyram)、代森联-锌、代森钠、甲基代森锌、福美双、硫威钠(vapam或metam sodium)、代森锌、福美锌、二甲基二硫醚(dithioether)、稻瘟灵、噻唑菌胺、三乙膦酸(fosetyl)、乙膦铝(疫霜灵)、溴甲烷、碘甲烷、异硫氰酸甲酯、环菌胺、甲呋酰胺、有效霉素、链霉素、(2RS)-2-溴-2-(溴甲基)戊二腈(溴菌腈)、多果定、十二烷基胍醋酸盐(doguadine)、双胍辛盐、双胍辛胺(iminoctadine)、双胍辛胺三乙酸盐、2,4-D、2,4-DB、春日霉素、甲菌定、环酰菌胺、恶霉灵、土菌消、抑霉唑、抑霉唑硫酸盐(imazalil sulphate)、恶咪唑、稻瘟酯、咪鲜胺、氟菌唑、咪唑菌酮、波尔多混合剂、多硫化钙、乙酸铜、碳酸铜、氢氧化铜、环烷酸铜、油酸铜、王铜、羟基喹啉铜、硅酸铜、硫酸铜、妥尔铜(copper tallate)、氧化亚铜、硫、西维因、稻瘟酞(四氯苯酞)、啶菌噁唑(dingjunezuo)(菌思奇)(Jun Si Qi)、氟噻唑吡乙酮(oxathiapiprolin)、氟里醚(fluoroimide)、双炔酰菌胺、KSF-1002、抑菌啉(benzamorf)、烯酰吗啉、丁苯吗啉、十三吗啉、十二环吗啉、乙霉威、三苯基乙酸锡、三苯基氢氧化锡、萎锈灵、氧化萎锈灵、敌菌酮、噁唑菌酮、间-苯基苯酚、对-苯基苯酚、三溴苯酚(TBP)、2-[2-[(7,8-二氟-2-甲基-3-喹啉基)氧基]-6-氟-苯基]丙烷-2-醇、2-[2-氟-6-[(8-氟-2-甲基-3-喹啉基)氧基]苯基]丙烷-2-醇、环氟菌胺、呋酰胺、恶霜灵、氟酰胺、灭锈胺、异丙噻菌胺(isofetamid)、拌种咯、咯菌腈、戊菌隆、克瘟散、异稻瘟净、定菌磷、磷酸、叶枯酞、敌菌丹、克菌丹、灭菌磷、嗪氨灵、苯锈啶、粉病灵、蛇床子素、1-甲基环丙烯、4-CPA、矮壮素、苯哒嗪酸、2,4-滴丙酸、噻节因、茵多酸、乙烯利、氟节胺、氯吡脲、赤霉酸、赤霉素、恶霉灵、马来酰肼、助壮素、萘乙酰胺、多效唑、调环酸、调环酸钙、噻苯隆、脱叶磷(三硫代磷酸三丁酯)、抗倒酸、烯效唑、α-萘乙酸、多氧菌素D(多抗霉素(polyoxrim))、BLAD、壳聚糖、氰菌胺、灭菌丹、3-(二氟甲基)-N-甲氧基-1-甲基-N-[1-甲基-2-(2,4,6-三氯苯基)乙基]吡唑-4-甲酰胺、联苯吡菌胺、氟唑菌酰胺、呋吡菌胺、吡唑萘菌胺、戊苯吡菌胺、吡噻菌胺、氟唑环菌胺、胺苯吡菌酮、哒菌酮、啶斑肟、啶酰菌胺、氟吡菌酰胺、二氟林、氯苯嘧啶醇、5-氟-2-(对-甲苯基甲氧基)嘧啶-4-胺、嘧菌腙、菌核净(dimetachlone或dimethaclone)、咯喹酮、丙氧喹啉、乙氧喹、喹氧灵、4,4,5-三氟-3,3-二甲基-1-(3-喹啉基)异喹啉、4,4-二氟-3,3-二甲基-1-(3-喹啉基)异喹啉、5-氟-3,3,4,4-四甲基-1-(3-喹啉基)异喹啉、9-氟-2,2-二甲基-5-(3-喹啉基)-3H-1,4-苯并氧杂吖庚因、异丁乙氧喹啉、噁喹酸(oxolinic acid)、灭螨猛(chinomethionate或oxythioquinox、quinoxymethionate)、螺环菌胺、(E)-N-甲基-2-[2-(2,5-二甲基苯氧基甲基)苯基]-2-甲氧基-亚氨基乙酰胺、(曼德斯宾)、嘧菌酯、丁香菌酯、醚菌胺、烯肟菌酯(enestroburin)、烯肟菌酯(enoxastrobin)、烯肟菌胺(fenamistrobin)、氟菌螨酯、氟嘧菌酯、醚菌酯、曼德斯宾、苯氧菌胺、叉氨苯酰胺、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、氯啶菌酯、肟菌酯、吲唑磺菌胺、抑菌灵、对甲抑菌灵、丁-3-炔基N-[6-[[(Z)-[(1-甲基四唑-5-基)-苯基-亚甲基]氨基]氧基甲基]-2-吡啶基]氨基甲酸酯、棉隆、异噻菌胺、噻酰菌胺、噻呋酰胺、苯噻硫氰(TCMTB)、硫硅菌胺、苯酰菌胺、防霉灵、三环唑、(.+-.)-顺式-1-(4-氯苯基)-2-(1H-1,2,4-三唑-1-基)-环庚醇(环菌唑(huanjunzuo))、1-(5-溴-2-吡啶基)-2-(2,4-二氟苯基)-1,1-二氟-3-(1,2,4-三唑-1-基)丙烷-2-醇、2-(1-叔丁基)-1-(2-氯苯基)-3-(1,2,4-三唑-1-基)-丙烷-2-醇(TCDP)、阿扎康唑、联苯三唑醇(双苯三唑醇)、糠菌唑、氯咪巴唑、环唑醇、苯醚甲环唑、地美康唑(dimetconazole)、烯唑醇、烯唑醇-M、氟环唑、乙环唑、腈苯唑、氟喹唑、氟硅唑、粉唑醇、己唑醇、亚胺唑、种菌唑、异芬特氟克那唑(ipfentrifluconazole)、叶菌唑、腈菌唑、戊菌唑、丙环唑、丙硫菌唑、硅氟唑、戊唑醇、四氟醚唑、三唑酮、三唑醇、咪唑嗪、灭菌唑、氯氟醚菌唑、2-[[(1R,5S)-5-[(4-氟苯基)甲基]-1-羟基-2,2-二甲基-环戊基]甲基]-4H-1,2,4-三唑-3-硫酮、2-[[3-(2-氯苯基)-2-(2,4-二氟苯基)环氧乙烷-2-基]甲基]-4H-1,2,4-三唑-3-硫酮、唑嘧菌胺(ametoctradin或imidium)、异丙菌胺、缬菌胺、2-苄基-4-氯酚(苄氯酚)、烯丙醇、唑啶草酮、苯扎氯铵、氯化苦、甲酚、达拉赛得(daracide)、二氯芬(双氯酚)、燕麦枯、双硫氧吡啶、N-(2-对氯苯甲酰基乙基)-六亚甲基四胺氯化物(N-(2-p-chlorobenzoylethyl)-hexaminium chloride)、NNF-0721、辛噻酮、环氧嘧磺隆、丙烷脒以及丙酸。
杀昆虫剂如阿维菌素、高灭磷、啶虫脒、磺胺螨酯(S-1955)、阿弗麦菌素、印楝素、甲基谷硫磷、联苯菊酯、联苯肼酯、噻嗪酮、克百威(carbofuran)、巴丹、氯虫苯甲酰胺(DPX-E2Y45)、溴虫腈、氟啶脲、毒死蜱、甲基毒死蜱、环虫酰肼、噻虫胺、丁氟螨酯、氟氯氰菊酯、β-氟氯氰菊酯、三氟氯氰菊酯、λ-三氯氟氰菊酯、氯氰菊酯、灭蝇胺、溴氰菊酯、丁醚脲、二嗪农、狄氏剂、除虫脲、四氟甲醚菊酯、乐果、呋虫胺、苯虫醚、埃玛菌素、硫丹、高氰戊菊酯、乙虫腈、苯硫威、苯氧威、甲氰菊酯、氰戊菊酯、氟虫腈、氟啶虫酰胺、氟虫双酰胺、氟氰戊菊酯、τ-氟胺氰菊酯、嘧虫胺(UR-50701)、氟虫脲、地虫硫磷、氯虫酰肼、氟铃脲、氟蚁腙、吡虫啉、茚虫威、异柳磷、虱螨脲、马拉硫磷、氰氟虫腙、四聚乙醛、甲胺磷、杀扑磷、灭多虫、烯虫酯、甲氧氯、甲氧苄氟菊酯、久效磷、甲氧虫酰肼、烯啶虫胺、硝乙脲噻唑、双苯氟脲、多氟脲(XDE-007)、杀线威、对硫磷、甲基对硫磷、苄氯菊酯、甲拌磷、伏杀磷、亚胺硫磷、磷胺、抗蚜威、丙溴磷、丙氟菊酯、吡蚜酮、啶吡唑虫胺、除虫菊酯、啶虫丙醚、氟虫吡喹、吡唑虫啶(pyriprole)、蚊蝇醚、鱼藤酮、利阿诺定、乙基多杀菌素、多杀菌素、螺螨酯、螺甲螨酯(BSN2060)、螺虫乙酯、硫丙磷、虫酰肼、氟苯脲、七氟菊酯、特丁硫磷、杀虫威、噻虫啉、噻虫嗪、硫双威、杀虫双、四溴菊酯、唑蚜威、敌百虫和杀虫隆;
杀细菌剂如链霉素;
杀螨剂如双甲脒、灭螨猛、乙酯杀螨醇、腈吡螨酯、三环锡、三氯杀螨醇、除螨灵、乙螨唑、喹螨醚、苯丁锡、甲氰菊酯、唑螨酯、噻螨酮、克螨特、哒螨灵和吡螨胺;并且
生物试剂如苏云金芽孢杆菌、苏云金芽孢杆菌δ内毒素、杆状病毒和昆虫病原细菌、病毒以及真菌。
“参考”混合物组合物的其他实例如下(其中术语“TX”表示选自如上文表X中所定义的化合物编号X.01、X.02、X.03或X.04的化合物(根据本发明组合物的组分(A)的定义):选自由以下组成的物质组的化合物:石油+TX、1,1-双(4-氯苯基)-2-乙氧基乙醇+TX、2,4-二氯苯基苯磺酸酯+TX、2-氟-N-甲基-N-1-萘乙酰胺+TX、4-氯苯基苯基砜+TX、乙酰虫腈+TX、涕灭砜威+TX、赛果+TX、果满磷+TX、胺吸磷+TX、草酸氢胺吸磷+TX、双甲脒+TX、杀螨特+TX、三氧化二砷+TX、偶氮苯+TX、偶氮磷+TX、苯菌灵+TX、苯诺沙磷(benoxa-fos)+TX、苯甲酸苄酯+TX、联苯吡菌胺+TX、溴灭菊酯+TX、溴虫氟苯双酰胺(broflanilide)+TX、溴烯杀+TX、溴硫磷+TX、溴螨酯+TX、噻嗪酮+TX、丁酮威+TX、丁酮砜威+TX、丁基哒螨灵+TX、多硫化钙+TX、八氯莰烯+TX、氯灭杀威+TX、三硫磷+TX、螨蜱胺+TX、灭螨猛+TX、杀螨醚+TX、杀虫脒+TX、杀虫脒盐酸盐+TX、杀螨醇+TX、杀螨酯+TX、敌螨特+TX、乙酯杀螨醇+TX、灭螨脒(chloromebuform)+TX、灭虫脲+TX、丙酯杀螨醇+TX、虫螨磷+TX、瓜菊酯I+TX、瓜菊酯II+TX、瓜菊酯+TX、克罗散泰+TX、蝇毒磷+TX、克罗米通+TX、巴毒磷+TX、硫杂灵+TX、果虫磷+TX、DCPM+TX、DDT+TX、田乐磷+TX、田乐磷-O+TX、田乐磷-S+TX、内吸磷-甲基+TX、内吸磷-O+TX、内吸磷-O-甲基+TX、内吸磷-S+TX、内吸磷-S-甲基+TX、磺吸磷(demeton-S-methylsulfon)+TX、抑菌灵+TX、敌敌畏+TX、二克磷(dicliphos)+TX、除螨灵+TX、甲氟磷+TX、消螨酚(dinex)+TX、消螨酚(dinex-diclexine)+TX、敌螨普-4+TX、敌螨普-6+TX、邻敌螨消+TX、硝戊酯+TX、硝辛酯杀螨剂+TX、硝丁酯+TX、敌杀磷+TX、磺基二苯+TX、戒酒硫+TX、DNOC+TX、苯氧炔螨(dofenapyn)+TX、多拉克汀+TX、因毒磷+TX、依立诺克丁+TX、益硫磷+TX、乙嘧硫磷+TX、抗螨唑+TX、苯丁锡+TX、苯硫威+TX、吡螨胺(fenpyrad)+TX、唑螨酯+TX、胺苯吡菌酮+TX、除螨酯+TX、氟硝二苯胺(fentrifanil)+TX、氟螨噻+TX、氟螨脲+TX、联氟螨+TX、氟杀螨+TX、FMC1137+TX、伐虫脒+TX、伐虫脒盐酸盐+TX、胺甲威(formparanate)+TX、γ-HCH+TX、果绿定+TX、苄螨醚+TX、十六烷基环丙烷羧酸酯+TX、水胺硫磷+TX、茉莉菊酯I+TX、茉莉菊酯II+TX、碘硫磷+TX、林丹+TX、丙螨氰+TX、灭蚜磷+TX、二噻磷+TX、甲硫芬+TX、虫螨畏+TX、溴甲烷+TX、速灭威+TX、自克威+TX、米尔贝肟+TX、丙胺氟+TX、久效磷+TX、茂果+TX、莫昔克丁+TX、二溴磷(naled)+TX、4-氯-2-(2-氯-2-甲基-丙基)-5-[(6-碘-3-吡啶基)甲氧基]哒嗪-3-酮+TX、氟蚁灵+TX、尼可霉素+TX、戊氰威+TX、戊氰威1:1氯化锌络合物+TX、氧乐果+TX、亚异砜磷+TX、砜拌磷+TX、pp'-DDT+TX、对硫磷+TX、苄氯菊酯+TX、芬硫磷+TX、伏杀磷+TX、硫环磷+TX、磷胺+TX、氯化松节油(polychloroterpenes)+TX、杀螨素(polynactins)+TX、丙氯诺+TX、蜱虱威+TX、残杀威+TX、乙噻唑磷+TX、发疏磷+TX、除虫菊酯I+TX、除虫菊酯II+TX、除虫菊酯+TX、哒嗪硫磷+TX、嘧硫磷+TX、喹硫磷(quinalphos)+TX、喹硫磷(quintiofos)+TX、R-1492+TX、甘氨硫磷+TX、鱼藤酮+TX、八甲磷+TX、克线丹+TX、司拉克丁+TX、苏硫磷+TX、SSI-121+TX、舒非仑+TX、氟虫胺+TX、硫特普+TX、硫+TX、氟螨嗪+TX、τ-氟胺氰菊酯+TX、TEPP+TX、叔丁威+TX、四氯杀螨砜+TX、杀螨好+TX、噻吩诺(thiafenox)+TX、抗虫威+TX、久效威+TX、甲基乙拌磷+TX、克杀螨+TX、苏力菌素+TX、威菌磷+TX、苯螨噻+TX、三唑磷+TX、灭蚜唑(triazuron)+TX、三氯丙氧磷+TX、三活菌素+TX、蚜灭多+TX、甲烯氟虫腈(vaniliprole)+TX、百杀辛(bethoxazin)+TX、二辛酸铜+TX、硫酸铜+TX、2-叔丁氨基-4-环丙氨基-6-甲硫基-s-三嗪(cybutryne)+TX、二氯萘醌+TX、双氯酚+TX、茵多酸+TX、三苯锡+TX、熟石灰+TX、代森钠+TX、灭藻醌+TX、醌萍胺+TX、西玛津+TX、三苯基乙酸锡+TX、三苯基氢氧化锡+TX、育畜磷+TX、哌嗪+TX、托布津+TX、氯醛糖+TX、倍硫磷+TX、吡啶-4-胺+TX、士的宁+TX、1-羟基-1H-吡啶-2-硫酮+TX、4-(喹喔啉-2-基氨基)苯磺酰胺+TX、8-羟基喹啉硫酸盐+TX、溴硝醇+TX、氢氧化铜+TX、甲酚+TX、双吡硫翁+TX、多地辛+TX、敌磺钠+TX、甲醛+TX、汞加芬+TX、春雷霉素+TX、春雷霉素盐酸盐水合物+TX、二(二甲基二硫代氨基甲酸)镍+TX、三氯甲基吡啶+TX、辛噻酮+TX、奥索利酸+TX、土霉素+TX、羟基喹啉硫酸钾+TX、噻菌灵+TX、链霉素+TX、链霉素倍半硫酸盐+TX、叶枯酞+TX、硫柳汞+TX、棉褐带卷蛾GV+TX、放射形土壤杆菌+TX、钝绥螨属物种(Amblyseius spp.)+TX、芹菜夜蛾NPV+TX、原樱翅缨小蜂(Anagrus atomus)+TX、短距蚜小蜂(Aphelinus abdominalis)+TX、棉蚜寄生蜂(Aphidius colemani)+TX、食蚜瘿蚊(Aphidoletes aphidimyza)+TX、苜蓿银纹夜蛾NPV+TX、球形芽孢杆菌(Bacillussphaericus Neide)+TX、布氏白僵菌(Beauveria brongniartii)+TX、普通草蛉(Chrysoperla carnea)+TX、孟氏隐唇瓢虫(Cryptolaemus montrouzieri)+TX、苹果蠹蛾GV+TX、西伯利亚离颚茧蜂(Dacnusa sibirica)+TX、豌豆潜叶蝇姬小蜂(Diglyphus isaea)+TX、丽蚜小蜂(Encarsia formosa)+TX、桨角蚜小蜂(Eretmocerus eremicus)+TX、嗜菌异小杆线虫(Heterorhabditis bacteriophora)和大异小杆线虫(H.megidis)+TX、斑长足瓢虫(Hippodamia convergens)+TX、橘粉介壳虫寄生蜂(Leptomastix dactylopii)+TX、盲蝽(Macrolophus caliginosus)+TX、甘蓝夜蛾NPV+TX、黄阔柄跳小蜂(Metaphycus helvolus)+TX、黄绿绿僵菌(Metarhizium anisopliae var.acridum)+TX、金龟子绿僵菌小孢变种(Metarhizium anisopliae var.anisopliae)+TX、欧洲新松叶蜂(Neodiprion sertifer)NPV和红头新松叶蜂(N.lecontei)NPV+TX、小花蝽属物种+TX、玫烟色拟青霉(Paecilomycesfumosoroseus)+TX、智利小植绥螨(Phytoseiulus persimilis)+TX、毛蚊线虫(Steinernema bibionis)+TX、小卷蛾斯氏线虫(Steinernema carpocapsae)+TX、夜蛾斯氏线虫+TX、格氏线虫(Steinernema glaseri)+TX、锐比斯氏线虫(Steinernema riobrave)+TX、莱奥博瑞斯斯氏线虫(Steinernema riobravis)+TX、蝼蛄斯氏线虫(Steinernemascapterisci)+TX、斯氏线虫属物种(Steinernema spp.)+TX、赤眼蜂属物种+TX、西方盲走螨(Typhlodromus occidentalis)+TX、蜡蚧轮枝菌(Verticillium lecanii)+TX、唑磷嗪(apholate)+TX、双(氮丙啶)甲氨基膦硫化物(bisazir)+TX、白消安+TX、迪麦替夫(dimatif)+TX、六甲蜜胺(hemel)+TX、六甲磷(hempa)+TX、甲基涕巴(metepa)+TX、甲硫涕巴(methiotepa)+TX、甲基唑磷嗪(methyl apholate)+TX、不孕啶(morzid)+TX、氟幼脲(penfluron)+TX、涕巴(tepa)+TX、硫代六甲磷(thiohempa)+TX、硫涕巴+TX、曲他胺+TX、尿烷亚胺+TX、(E)-癸-5-烯-1-基乙酸酯与(E)-癸-5-烯-1-醇+TX、(E)-十三碳-4-烯-1-基乙酸酯+TX、(E)-6-甲基庚-2-烯-4-醇+TX、(E,Z)-十四碳-4,10-二烯-1-基乙酸酯+TX、(Z)-十二碳-7-烯-1-基乙酸酯+TX、(Z)-十六碳-11-烯醛+TX、(Z)-十六碳-11-烯-1-基乙酸酯+TX、(Z)-十六碳-13-烯-11-炔-1-基乙酸酯+TX、(Z)-二十-13-烯-10-酮+TX、(Z)-十四碳-7-烯-1-醛+TX、(Z)-十四碳-9-烯-1-醇+TX、(Z)-十四碳-9-烯-1-基乙酸酯+TX、(7E,9Z)-十二碳-7,9-二烯-1-基乙酸酯+TX、(9Z,11E)-十四碳-9,11-二烯-1-基乙酸酯+TX、(9Z,12E)-十四碳-9,12-二烯-1-基乙酸酯+TX、14-甲基十八碳-1-烯+TX、4-甲基壬-5-醇与4-甲基壬-5-酮+TX、α-多纹素+TX、西部松小蠹集合信息素+TX、十二碳二烯醇(codlelure)+TX、可得蒙(codlemone)+TX、诱蝇酮(cuelure)+TX、环氧十九烷+TX、十二碳-8-烯-1-基乙酸酯+TX、十二碳-9-烯-1-基乙酸酯+TX、十二碳-8+TX、10-二烯-1-基乙酸酯+TX、谷蠹引诱剂(dominicalure)+TX、4-甲基辛酸乙酯+TX、丁香酚+TX、南部松小蠹集合信息素(frontalin)+TX、诱杀烯混剂(grandlure)+TX、诱杀烯混剂I+TX、诱杀烯混剂II+TX、诱杀烯混剂III+TX、诱杀烯混剂IV+TX、己诱剂(hexalure)+TX、齿小蠹二烯醇(ipsdienol)+TX、小蠢烯醇(ipsenol)+TX、金龟子性诱剂(japonilure)+TX、三甲基二氧三环壬烷(lineatin)+TX、夜蛾诱剂(litlure)+TX、粉纹夜蛾性诱剂(looplure)+TX、诱杀酯(medlure)+TX、美加特酸(megatomoic acid)+TX、诱虫醚(methyl eugenol)+TX、诱虫烯(muscalure)+TX、十八碳-2,13-二烯-1-基乙酸酯+TX、十八碳-3,13-二烯-1-基乙酸酯+TX、贺康彼(orfralure)+TX、椰蛀犀金龟聚集信息素(oryctalure)+TX、非乐康(ostramone)+TX、诱虫环(siglure)+TX、索迪叮(sordidin)+TX、食菌甲诱醇(sulcatol)+TX、十四碳-11-烯-1-基乙酸酯+TX、地中海实蝇引诱剂(trimedlure)+TX、地中海实蝇引诱剂A+TX、地中海实蝇引诱剂B1+TX、地中海实蝇引诱剂B2+TX、地中海实蝇引诱剂C+TX、突尼考(trunc-call)+TX、2-(辛基硫代)乙醇+TX、避蚊酮(butopyronoxyl)+TX、丁氧基(聚丙二醇)+TX、己二酸二丁酯+TX、邻苯二甲酸二丁酯+TX、丁二酸二丁酯+TX、避蚊胺+TX、驱蚊灵(dimethyl carbate)+TX、邻苯二甲酸二甲酯+TX、乙基己二醇+TX、己脲(hexamide)+TX、甲喹丁(methoquin-butyl)+TX、甲基新癸酰胺(methylneodecanamide)+TX、草氨酸盐(oxamate)+TX、派卡瑞丁(picaridin)+TX、1-二氯-1-硝基乙烷+TX、1,1-二氯-2,2-二(4-乙基苯基)-乙烷+TX、1,2-二氯丙烷与1,3-二氯丙烯+TX、1-溴-2-氯乙烷+TX、2,2,2-三氯-1-(3,4-二氯-苯基)乙基乙酸酯+TX、2,2-二氯乙烯基2-乙基亚磺酰基乙基甲基磷酸酯+TX、2-(1,3-二硫戊环-2-基)苯基二甲基氨基甲酸酯+TX、2-(2-丁氧基乙氧基)乙基硫氰酸酯+TX、2-(4,5-二甲基-1,3-二氧戊环-2-基)苯基甲基氨基甲酸酯+TX、2-(4-氯-3,5-二甲苯基氧基)乙醇+TX、2-氯乙烯基二乙基磷酸酯+TX、2-咪唑啉酮+TX、2-异戊酰茚满-1,3-二酮+TX、2-甲基(丙-2-炔基)氨基苯基甲基氨基甲酸酯+TX、2-氰硫基乙基月桂酸酯+TX、3-溴-1-氯丙-1-烯+TX、3-甲基-1-苯基吡唑-5-基二甲基-氨基甲酸酯+TX、4-甲基(丙-2-炔基)氨基-3,5-二甲苯基甲基氨基甲酸酯+TX、5,5-二甲基-3-氧代环己-1-烯基二甲基氨基甲酸酯+TX、阿赛硫磷+TX、丙烯腈+TX、艾氏剂+TX、阿洛氨菌素+TX、除害威+TX、α-蜕化素+TX、磷化铝+TX、灭害威+TX、新烟碱+TX、乙基杀扑磷(athidathion)+TX、甲基吡啶磷+TX、苏云金芽孢杆菌δ-内毒素+TX、六氟硅酸钡+TX、多硫化钡+TX、熏菊酯+TX、拜耳22/190+TX、拜耳22408+TX、β-氟氯氰菊酯+TX、β-氯氰菊酯+TX、戊环苄呋菊酯(bioethanomethrin)+TX、生物氯菊酯+TX、双(2-氯乙基)醚+TX、硼砂+TX、溴苯烯磷+TX、溴-DDT+TX、合杀威+TX、畜虫威+TX、特嘧硫磷(butathiofos)+TX、丁酯磷+TX、砷酸钙+TX、氰化钙+TX、二硫化碳+TX、四氯化碳+TX、巴丹盐酸盐+TX、瑟瓦定(cevadine)+TX、冰片丹+TX、氯丹+TX、十氯酮+TX、氯仿+TX、氯化苦+TX、氯腈肟磷+TX、氯吡唑磷(chlorprazophos)+TX、顺式苄呋菊酯(cis-resmethrin)+TX、顺式苄呋菊酯(cismethrin)+TX、氰菊酯(clocythrin)(别名)+TX、乙酰亚砷酸铜+TX、砷酸铜+TX、油酸铜+TX、畜虫磷(coumithoate)+TX、冰晶石+TX、CS 708+TX、苯腈磷+TX、杀螟腈+TX、环虫菊+TX、赛灭磷+TX、d-胺菊酯+TX、DAEP+TX、棉隆+TX、脱甲基克百威(decarbofuran)+TX、除线特(diamidafos)+TX、异氯磷+TX、除线磷+TX、迪克瑞塞(dicresyl)+TX、环虫腈+TX、狄氏剂+TX、二乙基5-甲基吡唑-3-基磷酸醋+TX、喘定(dior)+TX、四氟甲醚菊酯+TX、地麦威+TX、苄菊酯+TX、甲基毒虫畏+TX、敌蝇威+TX、丙硝酚+TX、戊硝酚+TX、地乐酚+TX、苯虫醚+TX、蔬果磷+TX、噻喃磷+TX、DSP+TX、脱皮甾酮+TX、EI 1642+TX、EMPC+TX、EPBP+TX、丙硫氧磷(etaphos)+TX、乙硫苯威+TX、甲酸乙酯+TX、二溴乙烷+TX、二氯乙烷+TX、环氧乙烷+TX、EXD+TX,皮蝇磷+TX、乙苯威+TX、杀螟硫磷+TX、氧嘧酰胺(fenoxacrim)+TX、吡氯氰菊酯+TX、丰索磷+TX、乙基倍硫磷+TX、氟氯双苯隆(flucofuron)+TX、丁苯硫磷+TX、磷砒酯+TX、丁环硫磷+TX、呋线威+TX、抗虫菊+TX、双胍辛盐+TX、双胍辛乙酸盐+TX、四硫代碳酸钠+TX、苄螨醚(halfenprox)+TX、HCH+TX、HEOD+TX、七氯+TX、速杀硫磷+TX、HHDN+TX、氰化氢+TX、喹啉威+TX、IPSP+TX、氯唑磷+TX、碳氯灵+TX、异艾氏剂+TX、异柳磷+TX、移栽灵+TX、稻瘟灵+TX、恶唑磷+TX、保幼激素I+TX、保幼激素II+TX、保幼激素III+TX、氯戊环+TX、烯虫炔酯+TX、砷酸铅+TX、溴苯磷+TX、啶虫磷+TX、噻唑磷+TX、间异丙苯基甲基氨基甲酸酯+TX、磷化镁+TX、叠氮磷+TX、甲基减蚜磷+TX、灭蚜硫磷+TX、氯化亚汞+TX、甲亚砜磷+TX、威百亩+TX、威百亩钾盐+TX、威百亩钠盐+TX、甲基磺酰氟+TX、丁烯胺磷+TX、甲氧普林+TX、甲醚菊酯+TX、甲氧滴滴涕+TX、异硫氰酸甲酯+TX、甲基氯仿+TX、二氯甲烷+TX、恶虫酮+TX、灭蚁灵+TX、奈肽磷+TX、萘+TX、NC-170+TX、烟碱+TX、硫酸烟碱+TX、硝虫噻嗪+TX、原烟碱+TX,O-5-二氯-4-碘代苯基O-乙基乙基硫代膦酸酯+TX、O,O-二乙基O-4-甲基-2-氧代-2H-苯并吡喃-7-基硫代膦酸酯+TX、O,O-二乙基O-6-甲基-2-丙基嘧啶-4-基硫代膦酸酯+TX、O,O,O',O'-四丙基二硫代焦磷酸酯+TX、油酸+TX、对-二氯苯+TX、甲基对硫磷+TX、五氯苯酚+TX、月桂酸五氯苯酯+TX、PH 60-38+TX、芬硫磷+TX、对氯硫磷+TX、磷化氢+TX、甲基辛硫磷+TX、甲胺嘧磷+TX、多氯二环戊二烯异构体+TX、亚砷酸钾+TX、硫氰酸钾+TX、早熟素I+TX、早熟素II+TX、早熟素III+TX、酰胺嘧啶磷+TX、丙氟菊酯+TX、猛杀威+TX、丙硫磷+TX、吡菌磷+TX、反灭虫菊+TX、苦木提取物(quassia)+TX、喹硫磷-甲基+TX、畜宁磷+TX、碘柳胺+TX、苄呋菊脂+TX、鱼藤酮+TX、噻嗯菊酯+TX、鱼尼汀+TX、利阿诺定+TX、沙巴藜芦(sabadilla)+TX、八甲磷+TX、克线丹+TX、SI-0009+TX、噻丙腈+TX、亚砷酸钠+TX、氰化钠+TX、氟化钠+TX、六氟硅酸钠+TX、五氯苯酚钠+TX,硒酸钠+TX,硫氰酸钠+TX、磺苯醚隆(sulcofuron)+TX,磺苯醚隆钠盐(sulcofuron-sodium)+TX,硫酰氟+TX,硫丙磷+TX、焦油+TX、噻螨威+TX、TDE+TX、丁基嘧啶磷+TX、双硫磷+TX、环戊烯丙菊酯+TX、四氯乙烷+TX、噻氯磷+TX、杀虫环+TX、杀虫环草酸盐+TX、虫线磷+TX、杀虫单+TX、杀虫单钠+TX、四溴菊酯+TX、反氯菊酯+TX、唑蚜威+TX、异皮蝇磷-3(trichlormetaphos-3)+TX、毒壤膦+TX、混杀威+TX、三氟甲氧威(tolprocarb)+TX、氯啶菌酯+TX、烯虫硫酯+TX、藜芦定+TX、藜芦碱+TX、XMC+TX、ζ-氯氰菊酯(zetamethrin)+TX、磷化锌+TX、唑虫磷+TX、以及氯氟醚菊酯+TX、四氟醚菊酯+TX、双(三丁基锡)氧化物+TX、溴乙酰胺+TX、磷酸铁+TX、氯硝柳胺-乙醇胺+TX、三丁基氧化锡+TX、吡吗啉+TX、蜗螺杀+TX、1,2-二溴-3-氯丙烷+TX、1,3-二氯丙烯+TX、3,4-二氯四氢噻吩1,1-二氧化物+TX、3-(4-氯苯基)-5-甲基罗丹宁+TX、5-甲基-6-硫代-1,3,5-噻二嗪-3-基乙酸+TX、6-异戊烯基氨基嘌呤+TX、2-氟-N-(3-甲氧基苯基)-9H-嘌呤-6-胺+TX、苯氯噻(benclothiaz)+TX、细胞分裂素+TX、DCIP+TX、糠醛+TX、异酰胺磷(isamidofos)+TX、激动素+TX、疣孢漆斑菌组合物+TX、四氯噻吩+TX、二甲苯酚+TX、玉米素+TX、乙基黄原酸钾+TX、阿拉酸式苯+TX、阿拉酸式苯-S-甲基+TX、大虎杖(Reynoutria sachalinensis)提取物+TX、α-氯代醇+TX、安妥+TX、碳酸钡+TX、双鼠脲+TX、溴鼠隆+TX、溴敌隆+TX、溴鼠胺+TX、氯鼠酮+TX、胆钙化醇+TX、氯杀鼠灵+TX、克灭鼠+TX、杀鼠萘+TX、杀鼠嘧啶+TX、鼠得克+TX、噻鼠灵+TX、敌鼠+TX、钙化醇+TX、氟鼠灵+TX、氟乙酰胺+TX、氟鼠啶+TX、氟鼠啶盐酸盐+TX、鼠特灵+TX、毒鼠磷+TX、磷+TX、杀鼠酮+TX、灭鼠优+TX、海葱糖苷+TX、氟乙酸钠+TX、硫酸铊+TX、杀鼠灵+TX、2-(-2-丁氧基乙氧基)乙基胡椒酸酯+TX、5-(1,3-苯并二氧杂环戊烯-5-基)-3-己基环己-2-烯酮+TX、具有橙花叔醇的法呢醇+TX、增效炔醚+TX、MGK 264+TX,增效醚+TX、增效醛+TX、增效酯(propyl isomer)+TX、S421+TX、增效散+TX、芝麻林素(sesasmolin)+TX、亚砜+TX、蒽醌+TX、环烷酸铜+TX、王铜+TX、二环戊二烯+TX、塞仑+TX、环烷酸锌+TX、福美锌+TX、衣马宁+TX、利巴韦林+TX、氯吲哚酰肼+TX、氧化汞+TX、甲基托布津+TX、阿扎康唑+TX、联苯三唑醇+TX、糠菌唑+TX、环唑醇+TX、苯醚甲环唑+TX、烯唑醇+TX、氟环唑+TX、腈苯唑+TX、氟喹唑+TX、氟硅唑+TX、粉唑醇+TX、呋吡菌胺+TX、己唑醇+TX、抑霉唑+TX、亚胺唑+TX、种菌唑+TX、叶菌唑+TX、腈菌唑+TX、多效唑+TX、稻瘟酯+TX、戊菌唑+TX、丙硫菌唑+TX、啶斑肟(pyrifenox)+TX、咪鲜胺+TX、丙环唑+TX、啶菌噁唑+TX、硅氟唑(simeconazole)+TX、戊唑醇+TX、氟醚唑+TX、三唑酮+TX、三唑醇+TX、氟菌唑+TX、灭菌唑+TX、嘧啶醇+TX、氯苯嘧啶醇+TX、氟苯嘧啶醇+TX、乙嘧酚磺酸酯(bupirimate)+TX、甲菌定(dimethirimol)+TX、乙菌定(ethirimol)+TX、十二环吗啉+TX、苯锈啶(fenpropidin)+TX、丁苯吗啉+TX、螺环菌胺+TX、十三吗啉+TX、嘧菌环胺+TX、嘧菌胺+TX、嘧霉胺(pyrimethanil)+TX;拌种咯+TX、咯菌腈+TX、苯霜灵(benalaxyl)+TX、呋霜灵(furalaxyl)+TX、甲霜灵+TX、R-甲霜灵+TX;呋酰胺+TX;恶霜灵(oxadixyl)+TX、多菌灵+TX、咪菌威(debacarb)+TX、麦穗宁+TX、噻苯达唑+TX、乙菌利(chlozolinate)+TX、菌核利(dichlozoline)+TX、甲菌利(myclozoline)+TX、腐霉利(procymidone)+TX、乙烯菌核利(vinclozoline)+TX、啶酰菌胺(boscalid)+TX、萎锈灵+TX、甲呋酰胺+TX、氟酰胺(flutolanil)+TX、灭锈胺+TX、氧化萎锈灵+TX、吡噻菌胺(penthiopyrad)+TX、噻呋酰胺+TX、多果定+TX、双胍辛胺+TX、嘧菌酯+TX、醚菌胺+TX、烯肟菌酯(enestroburin)+TX、烯肟菌胺+TX、氟菌螨酯+TX、氟嘧菌酯+TX、醚菌酯+TX、苯氧菌胺+TX、肟菌酯+TX、肟醚菌胺+TX、啶氧菌酯+TX、唑菌胺酯+TX、唑胺菌酯+TX、唑菌酯+TX、福美铁+TX、代森锰锌+TX、代森锰+TX、代森联+TX、甲基代森锌+TX、代森锌+TX、敌菌丹+TX、克菌丹+TX、氟里醚+TX、灭菌丹+TX、对甲抑菌灵+TX、波尔多混合剂+TX、氧化铜+TX、代森锰铜+TX、喹啉铜+TX、酞菌酯+TX、克瘟散+TX、异稻瘟净+TX、氯瘟磷+TX、甲基立枯磷+TX、敌菌灵+TX、苯噻菌胺+TX、灭瘟素(blasticidin)+TX、地茂散(chloroneb)+TX、百菌清+TX、环氟菌胺+TX、霜脲氰+TX、环丁氟仑(cyclobutrifluram)+TX、双氯氰菌胺(diclocymet)+TX、哒菌酮(diclomezine)+TX、氯硝胺(dicloran)+TX、乙霉威(diethofencarb)+TX、烯酰吗啉+TX、氟吗啉+TX、二噻农(dithianon)+TX、噻唑菌胺(ethaboxam)+TX、土菌灵(etridiazole)+TX、恶唑菌酮+TX、咪唑菌酮(fenamidone)+TX、稻瘟酰胺(fenoxanil)+TX、嘧菌腙(ferimzone)+TX、氟啶胺(fluazinam)+TX、氟吡菌胺(fluopicolide)+TX、磺菌胺(flusulfamide)+TX、氟唑菌酰胺+TX、环酰菌胺+TX、三乙膦酸铝(fosetyl-aluminium)+TX、恶霉灵(hymexazol)+TX、丙森锌+TX、赛座灭(cyazofamid)+TX、磺菌威(methasulfocarb)+TX、苯菌酮+TX、戊菌隆(pencycuron)+TX、苯酞+TX、多氧霉素(polyoxins)+TX、霜霉威(propamocarb)+TX、吡菌苯威+TX、碘喹唑酮(proquinazid)+TX、咯喹酮(pyroquilon)+TX、苯啶菌酮(pyriofenone)+TX、喹氧灵+TX、五氯硝基苯+TX、噻酰菌胺+TX、咪唑嗪(triazoxide)+TX、三环唑+TX、嗪氨灵+TX、有效霉素+TX、缬菌胺+TX、苯酰菌胺(zoxamide)+TX、双炔酰菌胺(mandipropamid)+TX、氟苯醚酰胺+TX、吡唑萘菌胺(isopyrazam)+TX、氟唑环菌胺(sedaxane)+TX、苯并烯氟菌唑+TX、氟唑菌酰羟胺+TX、3-二氟甲基-1-甲基-1H-吡唑-4-甲酸(3',4',5'-三氟-联苯-2-基)-酰胺+TX、异氟普兰(isoflucypram)+TX、异噻菌胺+TX、地芬灭替松(dipymetitrone)+TX、6-乙基-5,7-二氧代-吡咯并[4,5][1,4]二噻英并[1,2-c]异噻唑-3-甲腈+TX、2-(二氟甲基)-N-[3-乙基-1,1-二甲基-茚满-4-基]吡啶-3-甲酰胺+TX、4-(2,6-二氟苯基)-6-甲基-5-苯基-哒嗪-3-甲腈+TX、(R)-3-(二氟甲基)-1-甲基-N-[1,1,3-三甲基茚满-4-基]吡唑-4-甲酰胺+TX、4-(2-溴-4-氟-苯基)-N-(2-氯-6-氟-苯基)-2,5-二甲基-吡唑-3-胺+TX、4-(2-溴-4-氟苯基)-N-(2-氯-6-氟苯基)-1,3-二甲基-1H-吡唑-5-胺+TX、氟茚唑菌胺(fluindapyr)+TX、甲香菌酯(jiaxiangjunzhi)+TX、鲁本米西安(lvbenmixianan)+TX、二氯苯偶氮(dichlobentiazox)+TX、曼德斯宾(mandestrobin)+TX、3-(4,4-二氟-3,4-二氢-3,3-二甲基异喹啉-1-基)喹诺酮+TX、2-[2-氟-6-[(8-氟-2-甲基-3-喹啉基)氧基]苯基]丙-2-醇+TX、氟噻唑吡乙酮(oxathiapiprolin)+TX、N-[6-[[[(1-甲基四唑-5-基)-苯基-亚甲基]氨基]氧基甲基]-2-吡啶基]氨基甲酸叔丁酯+TX、联苯吡嗪菌胺(pyraziflumid)+TX、英派尔福沙姆(inpyrfluxam)+TX、曲普卡(trolprocarb)+TX、氯氟醚菌唑+TX、异芬特氟克那唑(ipfentrifluconazole)+TX、2-(二氟甲基)-N-[(3R)-3-乙基-1,1-二甲基-茚满-4-基]吡啶-3-甲酰胺+TX、N'-(2,5-二甲基-4-苯氧基-苯基)-N-乙基-N-甲基-甲脒+TX、N'-[4-(4,5-二氯噻唑-2-基)氧基-2,5-二甲基-苯基]-N-乙基-N-甲基-甲脒+TX、[2-[3-[2-[1-[2-[3,5-双(二氟甲基)吡唑-1-基]乙酰基]-4-哌啶基]噻唑-4-基]-4,5-二氢异噁唑-5-基]-3-氯-苯基]甲磺酸盐+TX、N-[6-[[(Z)-[(1-甲基四唑-5-基)-苯基-亚甲基]氨基]氧基甲基]-2-吡啶基]氨基甲酸丁-3-炔酯+TX、N-[[5-[4-(2,4-二甲基苯基)三唑-2-基]-2-甲基-苯基]甲基]氨基甲酸甲酯+TX、3-氯-6-甲基-5-苯基-4-(2,4,6-三氟苯基)哒嗪+TX、吡啶达氯甲基(pyridachlometyl)+TX、3-(二氟甲基)-1-甲基-N-[1,1,3-三甲基茚满-4-基]吡唑-4-甲酰胺+TX、1-[2-[[1-(4-氯苯基)吡唑-3-基]氧基甲基]-3-甲基-苯基]-4-甲基-四唑-5-酮+TX、1-甲基-4-[3-甲基-2-[[2-甲基-4-(3,4,5-三甲基吡唑-1-基)苯氧基]甲基]苯基]四唑-5-酮+TX、爱米诺庇力芬(aminopyrifen)+TX、唑嘧菌胺+TX、吲唑磺菌胺+TX、氟唑菌苯胺+TX、(Z,2E)-5-[1-(4-氯苯基)吡唑-3-基]氧基-2-甲氧基亚氨基-N,3-二甲基-戊-3-烯酰胺+TX、吡啶菌酰胺+TX、芬庇科米得(fenpicoxamid)+TX、异丁乙氧喹啉+TX、氟苯喹(ipflufenoquin)+TX、奎诺福林(quinofumelin)+TX、异丙噻菌胺+TX、N-[2-[2,4-二氯-苯氧基]苯基]-3-(二氟甲基)-1-甲基-吡唑-4-甲酰胺+TX、N-[2-[2-氯-4-(三氟甲基)苯氧基]苯基]-3-(二氟甲基)-1-甲基-吡唑-4-甲酰胺+TX、苯噻菌酯+TX、氰烯菌酯+TX、5-氨基-1,3,4-噻二唑-2-硫醇锌盐(2:1)+TX、氟吡菌酰胺+TX、氟噻唑菌腈+TX、氟醚菌酰胺+TX、吡丙炔(pyrapropoyne)+TX、哌碳唑(picarbutrazox)+TX、2-(二氟甲基)-N-(3-乙基-1,1-二甲基-茚满-4-基)吡啶-3-甲酰胺+TX、2-(二氟甲基)-N-((3R)-1,1,3-三甲基茚满-4-基)吡啶-3-甲酰胺+TX、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈+TX、美特尔特特拉普罗(metyltetraprole)+TX、2-(二氟甲基)-N-((3R)-1,1,3-三甲基茚满-4-基)吡啶-3-甲酰胺+TX、α-(1,1-二甲基乙基)-α-[4'-(三氟甲氧基)[1,1'-二苯基]-4-基]-5-嘧啶甲醇+TX、氟哌啶(fluoxapiprolin)+TX、烯肟菌酯(enoxastrobin)+TX、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈+TX、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(5-硫烷基-1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈+TX、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(5-硫代-4H-1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈+TX、抗倒酸+TX、丁香菌酯+TX、中生菌素+TX、噻菌铜+TX、噻唑锌+TX、苯唑嘧菌胺(amectotractin)+TX、异菌脲+TX、N-辛-N'-[2-(辛氨基)乙基]乙烷-1,2-二胺+TX;N'-[5-溴-2-甲基-6-[(1S)-1-甲基-2-丙氧基-乙氧基]-3-吡啶基]-N-乙基-N-甲基-甲脒+TX、N'-[5-溴-2-甲基-6-[(1R)-1-甲基-2-丙氧基-乙氧基]-3-吡啶基]-N-乙基-N-甲基-甲脒+TX、N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒+TX、N'-[5-氯-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒+TX、N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-异丙基-N-甲基-甲脒+TX(这些化合物可以由WO 2015/155075中描述的方法制备);N'-[5-溴-2-甲基-6-(2-丙氧基丙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒+TX(此种化合物可以由IPCOM000249876D中描述的方法制备);N-异丙基-N’-[5-甲氧基-2-甲基-4-(2,2,2-三氟-1-羟基-1-苯基-乙基)苯基]-N-甲基-甲脒+TX、N’-[4-(1-环丙基-2,2,2-三氟-1-羟基-乙基)-5-甲氧基-2-甲基-苯基]-N-异丙基-N-甲基-甲脒+TX(这些化合物可以由WO2018/228896中描述的方法制备);N-乙基-N’-[5-甲氧基-2-甲基-4-[2-三氟甲基)氧杂环丁烷-2-基]苯基]-N-甲基-甲脒+TX、N-乙基-N’-[5-甲氧基-2-甲基-4-[2-三氟甲基)四氢呋喃-2-基]苯基]-N-甲基-甲脒+TX(这些化合物可以由WO 2019/110427中描述的方法制备);N-[(1R)-1-苄基-3-氯-1-甲基-丁-3-烯基]-8-氟-喹啉-3-甲酰胺+TX、N-[(1S)-1-苄基-3-氯-1-甲基-丁-3-烯基]-8-氟-喹啉-3-甲酰胺+TX、N-[(1R)-1-苄基-3,3,3-三氟-1-甲基-丙基]-8-氟-喹啉-3-甲酰胺+TX、N-[(1S)-1-苄基-3,3,3-三氟-1-甲基-丙基]-8-氟-喹啉-3-甲酰胺+TX、N-[(1R)-1-苄基-1,3-二甲基-丁基]-7,8-二氟-喹啉-3-甲酰胺+TX、N-[(1S)-1-苄基-1,3-二甲基-丁基]-7,8-二氟-喹啉-3-甲酰胺+TX、8-氟-N-[(1R)-1-[(3-氟苯基)甲基]-1,3-二甲基-丁基]喹啉-3-甲酰胺+TX、8-氟-N-[(1S)-1-[(3-氟苯基)甲基]-1,3-二甲基-丁基]喹啉-3-甲酰胺+TX、N-[(1R)-1-苄基-1,3-二甲基-丁基]-8-氟-喹啉-3-甲酰胺+TX、N-[(1S)-1-苄基-1,3-二甲基-丁基]-8-氟-喹啉-3-甲酰胺+TX、N-((1R)-1-苄基-3-氯-1-甲基-丁-3-烯基)-8-氟-喹啉-3-甲酰胺+TX、N-((1S)-1-苄基-3-氯-1-甲基-丁-3-烯基)-8-氟-喹啉-3-甲酰胺+TX(这些化合物可以由WO 2017/153380中描述的方法制备);
1-(6,7-二甲基吡唑并[1,5-a]吡啶-3-基)-4,4,5-三氟-3,3-二甲基-异喹啉+TX、1-(6,7-二甲基吡唑并[1,5-a]吡啶-3-基)-4,4,6-三氟-3,3-二甲基-异喹啉+TX、4,4-二氟-3,3-二甲基-1-(6-甲基吡唑并[1,5-a]吡啶-3-基)异喹啉+TX、4,4-二氟-3,3-二甲基-1-(7-甲基吡唑并[1,5-a]吡啶-3-基)异喹啉+TX、1-(6-氯-7-甲基-吡唑并[1,5-a]吡啶-3-基)-4,4-二氟-3,3-二甲基-异喹啉+TX(这些化合物可以由WO 2017/025510中描述的方法制备);1-(4,5-二甲基苯并咪唑-1-基)-4,4,5-三氟-3,3-二甲基-异喹啉+TX、1-(4,5-二甲基苯并咪唑-1-基)-4,4-二氟-3,3-二甲基-异喹啉+TX、6-氯-4,4-二氟-3,3-二甲基-1-(4-甲基苯并咪唑-1-基)异喹啉+TX、4,4-二氟-1-(5-氟-4-甲基-苯并咪唑-1-基)-3,3-二甲基-异喹啉+TX、3-(4,4-二氟-3,3-二甲基-1-异喹啉基)-7,8-二氢-6H-环戊二烯并[e]苯并咪唑+TX(这些化合物可以由WO 2016/156085中描述的方法制备);[(1S,2S)-1-甲基-2-(邻甲苯基)丙基](2S)-2-[(3-羟基-4-甲氧基-吡啶-2-羰基)氨基]丙酸酯+TX、[(1S,2S)-1-甲基-2-(邻甲苯基)丙基](2S)-2-[(3-乙酰氧基-4-甲氧基-吡啶-2-羰基)氨基]丙酸酯+TX、[(1S,2S)-1-甲基-2-(邻甲苯基)丙基](2S)-2-[(4-甲氧基-3-丙酰基氧基-吡啶-2-羰基)氨基]丙酸酯+TX、[(1S,2S)-2-(4-氟-2-甲基-苯基)-1,3-二甲基-丁基](2S)-2-[(3-羟基-4-甲氧基-吡啶-2-羰基)氨基]丙酸酯+TX、[(1S,2S)-2-(4-氟-2-甲基-苯基)-1,3-二甲基-丁基](2S)-2-[(3-乙酰氧基-4-甲氧基-吡啶-2-羰基)氨基]丙酸酯+TX、[(1S,2S)-2-(4-氟-2-甲基-苯基)-1,3-二甲基-丁基](2S)-2-[(4-甲氧基-3-丙酰基氧基-吡啶-2-羰基)氨基]丙酸酯+TX、N-甲氧基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]环丙烷甲酰胺+TX、N,2-二甲氧基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺+TX、N-乙基-2-甲基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺+TX、1-甲氧基-3-甲基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲+TX、1,3-二甲氧基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲+TX、3-乙基-1-甲氧基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲+TX、N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺+TX、4,4-二甲基-2-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]异噁唑烷-3-酮+TX、5,5-二甲基-2-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]异噁唑烷-3-酮+TX、1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]吡唑-4-甲酸乙酯+TX、N,N-二甲基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]-1,2,4-三唑-3-胺+TX。此段落中的化合物可以由WO 2017/055473、WO 2017/055469、WO 2017/093348和WO 2017/118689中描述的方法制备;2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇+TX(此化合物可以由WO 2017/029179中描述的方法制备);2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇+TX(此化合物可以由WO 2017/029179中描述的方法制备);3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈+TX(此化合物可以由WO 2016/156290中描述的方法制备);3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈+TX(此化合物可以由WO 2016/156290中描述的方法制备);2-氨基-6-甲基-吡啶-3-甲酸(4-苯氧基苯基)甲酯+TX(此化合物可以由WO 2014/006945中描述的方法制备);2,6-二甲基-1H,5H-[1,4]二噻英并[2,3-c:5,6-c']二吡咯-1,3,5,7(2H,6H)-四酮+TX(此化合物可以由WO2011/138281中描述的方法制备);N-甲基-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]硫代苯甲酰胺+TX;N-甲基-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺+TX;(Z,2E)-5-[1-(2,4-二氯苯基)吡唑-3-基]氧基-2-甲氧基亚氨基-N,3-二甲基-戊-3-烯酰胺+TX(此化合物可以由WO 2018/153707中描述的方法制备);N'-(2-氯-5-甲基-4-苯氧基-苯基)-N-乙基-N-甲基-甲脒+TX;N'-[2-氯-4-(2-氟苯氧基)-5-甲基-苯基]-N-乙基-N-甲基-甲脒+TX(此化合物可以由WO 2016/202742中描述的方法制备);2-(二氟甲基)-N-[(3S)-3-乙基-1,1-二甲基-茚满-4-基]吡啶-3-甲酰胺+TX(此化合物可以由WO 2014/095675中描述的方法制备);(5-甲基-2-吡啶基)-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲酮+TX、(3-甲基异噁唑-5-基)-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲酮+TX(这些化合物可以由WO 2017/220485中描述的方法制备);2-氧代-N-丙基-2-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]乙酰胺+TX(此化合物可以由WO 2018/065414中描述的方法制备);1-[[5-[5-(三氟甲基)-1,2,4-噁二唑-3-基]-2-噻吩基]甲基]吡唑-4-甲酸乙酯+TX(此化合物可以由WO 2018/158365中描述的方法制备);2,2-二氟-N-甲基-2-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]乙酰胺+TX、N-[(E)-甲氧基亚氨基甲基]-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺+TX、N-[(Z)-甲氧基亚氨基甲基]-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺+TX、N-[N-甲氧基-C-甲基-碳亚氨基]-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺+TX(这些化合物可以由WO 2018/202428中描述的方法制备)、生物刺激素(QuantisTM)(其包含有机碳、营养素和氨基酸)+TX。
在活性成分之后的括号中的参考例如[3878-19-1]是指化学文摘登记号。上文描述的混合配伍物是已知的。在活性成分包括在“The Pesticide Manual[杀有害生物剂手册]”[The Pesticide Manual-A World Compendium[杀有害生物剂手册-全球概览];第13版;编辑:C.D.S.TomLin;The British Crop Protection Coimcil[英国农作物保护委员会]]中的情况下,它们在其中以上文对于特定化合物的圆括号中所给出的条目编号来描述;例如化合物“阿维菌素”以条目编号(1)来描述。在“[CCN]”在上文添加到特定化合物的情况下,所述的化合物包括在“Compendium of Pesticide Common Names[杀有害生物剂通用名纲要]”中,其可以在互联网[A.Wood;Compendium of Pesticide Common Names,1995-2004]上获得;例如,化合物“乙酰虫腈”描述于互联网地址http:// www.alanwood.net/pesticides/acetoprole.html
多数上述活性成分在上文中通过所谓的“通用名”来提及,在单个情形中使用相应的“ISO通用名”或另一“通用名”。若名称不是“通用名”,则所使用的名称种类以特定化合物的圆括号中所给出的名称来代替;在这种情况下,使用IUPAC名称、IUPAC/化学文摘名、“化学名称”、“惯用名”、“化合物名称”或“开发代码”,或若既不使用那些名称之一也不使用“通用名”,则使用“别名”。“CAS登记号”意指化学文摘登记号。
在“参考”混合物组合物中,具有式(I)的化合物(选自表X(上文))与以上描述的活性成分的混合物包括选自表X(上文)的化合物和如以上描述的活性成分,其优选地是处于从100:1至1:100的混合比率,尤其是从50:1至1:50,更尤其是处于从20:1至1:20的比率,甚至更尤其是从10:1至1:10,又甚至更尤其是从7.5:1至1:7.5,非常尤其是从5:1和1:5,特别优选地是从2:1至1:2的比率,并且从4:1至2:1的比率同样是优选的,尤其是处于1:1、或5:1、或5:2、或5:3、或5:4、或4:1、或4:2、或4:3、或3:1、或3:2、或2:1、或1:5、或2:5、或3:5、或4:5、或1:4、或2:4、或3:4、或1:3、或2:3、或1:2、或1:600、或1:300、或1:150、或1:35、或2:35、或4:35、或1:75、或2:75、或4:75、或1:6000、或1:3000、或1:1500、或1:350、或2:350、或4:350、或1:750、或2:750、或4:750的比率。那些混合比率是按重量计的。
可以将如上描述的这些混合组合物(均根据本发明和“参考”混合组合物)用于控制有害生物的方法中,该方法包括将含如上描述的混合物的组合物施用于有害生物或其环境中。
包含选自表X(以上)的具有式(I)的化合物以及一种或多种如以上描述的活性成分的混合物可以例如以单一的“掺水即用”的形式施用,以组合的喷洒混合物(该混合物由这些单一活性成分的单独配制品构成)(如一种“桶混制剂”)施用,并且当以一种顺序的方式(即,一个在另一个适度短的时期之后,例如几小时或几天)施用时组合使用这些单独活性成分来施用。施用选自表X(以上)的具有式(I)的这些化合物和如上描述的这些活性成分的顺序对于实施本发明并不是重要的。
本发明的这些组合物还可以用于作物增强。根据本发明,‘作物增强’意指植物活力的改善、植物品质的改善,对于胁迫因素的改善的耐受力和/或改善的投入利用效率。
根据本发明,‘植物活力的改善’意指当与已经在相同条件下生长但未使用本发明的方法的对照植物的相同性状相比时,某些性状在质量或数量上被改善。这样的性状包括,但并不局限于,早的和/或改善的发芽,改善的出苗,使用更少种子的能力,增加的根的生长,更发达的根系,增加的根的结瘤,增加的芽的生长,增加的分蘖,更强的分蘖,更有效的分蘖,增加的或改善的植物站立,更少的植物颠倒(plant verse)(倒伏),植物高度的增加和/或改善,植物重量(鲜重或干重)的增加,更大的叶片,更绿的叶子颜色,增加的颜料含量,增加的光合活性,更早的开花,更长的圆锥花序,早的谷物成熟期,增加的种子、果实或荚果大小,增加的荚果或穗的数量,增加的每荚果或穗的种子数量,增加的种子品质,增强的种子填充,更少的死的基生叶,延缓枯萎,改善的植物生命力,在储存组织的提高的氨基酸类化合物水平和/或需要更少的投入(例如更少的所需肥料、水和/或劳作)。活力改善的植物可以具有在任何上述性状或任意组合或两个或更多个上述性状方面的增加。
根据本发明,‘植物品质的改善’意指当与已经在相同条件下生长但未使用本发明的方法的对照植物的相同性状相比时,某些性状在质量或数量上被改善。这样的性状包括,但并不局限于,改善的植物视觉外观,减少的乙烯(减少产生和/或抑制接收),所收获材料(例如种子、果实、叶、蔬菜)的改善的品质,(这样改善的品质可以表现为所收获材料的改善的视觉外观,改善的碳水化合物含量(例如增加的糖和/或淀粉的量值、改善的糖酸比、还原糖的减少、增加的糖形成速度),改善的蛋白质含量,改善的油含量和组成,改善的营养价值,抗营养化合物的减少,改善的感官特性(例如改善的味道)和/或改善的消费者健康益处(例如增加的维生素和抗氧化剂水平)),改善的收获后特征(例如增强的贮存期和/或贮存稳定性,更容易的可加工性,更容易的化合物提取),更同质的作物发育(例如植物的同时萌发、开花和/或结果)和/或改善的种子品质(例如在随后的季节中使用)。品质改善的植物可以具有在任何上述这些性状或任意组合或两个或更多个上述性状方面的增加。
根据本发明,对胁迫因素的耐受性改良表示某些性状与在缺少本发明方法的相同条件下的对照植物的相同性状相比时定性地或定量地得到改良。这样的性状包括但并不局限于对多种非生物胁迫因素的耐受力和/或抗性增加,这些因素引发次优生长条件,如干旱(例如导致植物水含量缺乏、水吸收潜力缺乏或向植物供水减少的任何胁迫)、受冷、受热、渗透胁迫、UV胁迫、漫灌、盐度增加(例如土壤中的盐度)、增加的矿物暴露、臭氧暴露、高度的光暴露和/或养分(例如氮和/或磷养分)利用受限。对胁迫因素的耐受性改善的植物可以具有在任何上述性状或任意组合或两个或更多个上述性状方面的增加。在干旱和养分胁迫的情况下,这些耐受性改善可以归因于,例如,更高效率的吸收、利用或者保有水分和养分。
根据本发明,‘改善的投入利用效率’意指当与在相同条件下生长但未使用本发明的方法的对照植物的生长相比时,植物能够更有效地使用给定的投入水平而生长。具体而言,这些投入包括,但并不限于肥料(如氮、磷、钾、微量营养素)、光和水。具有改善的投入利用效率的植物可以具有对任何上述投入、或两种或更多种上述投入的任何组合的改善的使用。
本发明的其他作物增强包括减少植物高度,或减少分蘖,这在作物中或在希望具有更少的生物质和更少分蘖的条件下是有益的特征。
任何或全部以上的作物增强可以通过改善例如植物生理、植物生长与发育和/或植物株型而导致改善的产量。在本发明的上下文中,‘产量’包括,但并不局限于:(i)生物质生产、谷物产量、淀粉含量、油含量和/或蛋白质含量的增加,这可以起因于:(a)由植物自身生产的量的增加或(b)改善的收获植物物质的能力,(ii)收获材料的组成上的改善(例如改善的糖酸比、改善的油组成,增加的营养价值,抗营养化合物的减少,增加的消费者健康益处)和/或(iii)增加的/易化的收获作物的能力、改善的作物可加工性和/或更好的贮存稳定性/贮存期。农业植物的产量增加意指,在可能采取定量测量的情况下,各个植物的某一产物的产量比该植物在相同条件下(但没有应用本发明)生产的这种相同产物的产量提高可测量的数量。根据本发明,优选该产量提高至少0.5%、更优选至少1%、甚至更优选至少2%、仍更优选至少4%、优选5%或甚至更高。
任何或全部以上的作物增强也可以导致土地利用改善,即,先前对于种植不可用或次优的土地可以变得可用。例如,在干旱条件下显示出生存能力增强的植物能够在次优降雨地区(例如可能在沙漠边缘或者甚至沙漠里)种植。
在本发明的一个方面,作物增强是在来自有害生物和/或病害和/或非生物胁迫的压力大体上不存在下得到的。在本发明的另一个方面,植物活力、胁迫耐受力、品质和/或产量的改善是在来自有害生物和/或病害的压力大体上不存在下得到的。例如,有害生物和/或病害可以通过在本发明的方法之前,或者同时施用杀有害生物处理来控制。在本发明的还另一个方面,植物活力、胁迫耐受力、品质和/或产量的改善是在有害生物和/或病害压力不存在下得到的。在另外的实施例中,植物活力、品质和/或产量的改善是在非生物胁迫不存在或者大体上不存在下得到的。
本发明的这些组合物还可以在保护储存货物免受真菌攻击的领域中使用。根据本发明,术语“储存货物”应被理解为表示植物和/或动物来源的天然物质及其加工形式,其取自天然生命周期并且其被希望用于长期保护。植物来源的储存货物(如植物或其部分(例如,茎秆、叶子、块茎、种子、果实或谷粒))可以以新鲜收割的状态或以加工形式(如预干燥的、润湿的、粉碎的、磨碎的或烘烤的)进行保护。也落在储存货物定义下的是木材,无论为原木形式,如建筑木材、输电塔和栅栏,或为制成品形式,如从木材制造的家具或物体。动物来源的储存货物是兽皮、革、毛皮、毛发等。根据本发明的组合物可以预防不利的作用,如腐败、褪色或发霉。优选地,“储存货物”应被理解为表示植物来源的天然物质和/或其加工形式,更优选水果及其加工形式(如梨果、核果、浆果和柑橘及其加工形式)。在本发明的另一个优选的实施例中,“储存货物”应被理解为表示木材。
因此,本发明的另一个方面是保护储存货物的方法,该方法包括将根据本发明的组合物施用至储存货物。
本发明的组合物还可以在保护技术材料免受真菌攻击的领域中使用。根据本发明,术语“技术材料”包括纸;毯;建筑;冷却和加热系统;墙板;通风和空调系统等;优选地,“技术材料”应被理解为表示墙板。根据本发明的组合物可以预防不利的作用,如腐败、褪色或发霉。
根据本发明的组合物通常使用配制辅助剂(如载体、溶剂和表面活性物质)以多种方式配制。这些配制品可以处于不同的实体形式,例如,处于以下形式:撒粉剂、凝胶、可湿性粉剂、水可分散性颗粒剂、水可分散性片剂、泡腾压缩片剂、可乳化的浓缩物、微可乳化浓缩物、水包油乳剂、可流动油、水性分散体、油性分散体、悬乳剂、胶囊悬浮液、可乳化的颗粒剂、可溶性液体、水可溶性浓缩物(以水或水混溶性有机溶剂作为载体)、浸渍的聚合物膜或处于已知的其他形式,例如从Manual on Development and Use of FAO and WHOSpecifications for Pesticides[关于杀有害生物剂的FAO和WHO标准的发展和使用的手册],联合国,第1版,二次修订(2010)中已知的。此类配制品可以直接使用或者可以使用前稀释再使用。可以用例如水、液体肥料、微量营养素、生物有机体、油或溶剂来进行稀释。
可以通过例如将活性成分与配制辅助剂混合来制备这些配制品以便获得处于精细分散固体、颗粒、溶液、分散体或乳剂形式的组合物。这些活性成分还可以与其他辅助剂(例如精细分散固体、矿物油、植物或动物来源的油、改性的植物或动物来源的油、有机溶剂、水、表面活性物质或其组合)来一起配制。
这些活性成分还可以被包含于微胶囊中。微胶囊在多孔载体中含有活性成分。这使得活性成分能够以受控的量释放(例如,缓慢释放)到环境中。微胶囊通常具有从0.1至500微米的直径。它们包含的活性成分的量按重量计是胶囊重量的约从25%至95%。这些活性成分可以处于整体性的固体的形式、处于固体或液体分散体中的精细颗粒的形式或处于适合溶液的形式。包囊的膜可以包含例如天然的或合成的橡胶、纤维素、苯乙烯/丁二烯共聚物、聚丙烯腈、聚丙烯酸酯、聚酯、聚酰胺、聚脲、聚氨酯或化学改性的聚合物以及淀粉黄原酸酯、或本领域的技术人员已知的其他聚合物。可替代地,可以形成非常精细的微胶囊,其中活性成分在基础物质的固体基质中是以精细分散颗粒的形式被包含的,但这些微胶囊本身未经包裹。
适合于制备根据本发明的配制品的配制辅助剂本身是已知的。作为液体载体可以使用:水、甲苯、二甲苯、石油醚、植物油、丙酮、甲基乙基酮、环己酮、酸酐、乙腈、乙酰苯、乙酸戊酯、2-丁酮、碳酸丁烯酯、氯苯、环己烷、环己醇、乙酸烷基酯、二丙酮醇、1,2-二氯丙烷、二乙醇胺、对-二乙基苯、二甘醇、松脂酸二乙二醇酯、二甘醇丁基醚、二甘醇乙基醚、二甘醇甲醚、N,N-二甲基甲酰胺、二甲基亚砜、1,4-二噁烷、二丙二醇、二丙二醇甲基醚、双丙甘醇二苯甲酸酯、二丙二醇、烷基吡咯烷酮、乙酸乙酯、2-乙基己醇、碳酸乙烯酯、1,1,1-三氯乙烷、2-庚酮、α-蒎烯、d-苧烯、乳酸乙酯、乙二醇、乙二醇丁基醚、乙二醇甲基醚、γ-丁内酯、丙三醇、乙酸甘油酯、二乙酸甘油酯、三乙酸甘油酯、十六烷、己二醇、乙酸异戊基酯、乙酸异冰片基酯、异辛烷、异佛尔酮、异丙苯、肉豆蔻酸异丙酯、乳酸、月桂胺、异亚丙基丙酮、甲氧基丙醇、甲基异戊基酮、甲基异丁基酮、月桂酸甲酯、辛酸甲酯、油酸甲酯、二氯甲烷、间二甲苯、正己烷、正辛胺、十八烷酸、辛胺乙酸酯、油酸、油烯基胺、邻二甲苯、苯酚、聚乙二醇、丙酸、乳酸丙酯、碳酸亚丙酯、丙二醇、丙二醇甲基醚、对-二甲苯、甲苯、磷酸三乙酯、三乙二醇、二甲苯磺酸、石蜡、矿物油、三氯乙烯、全氯乙烯、乙酸乙酯、乙酸戊酯、乙酸丁酯、丙二醇甲基醚、二乙二醇甲基醚、甲醇、乙醇、异丙醇以及更高分子量的醇,例如戊醇、四氢呋喃醇、己醇、辛醇、乙二醇、丙二醇、甘油、N-甲基-2-吡咯烷酮等。
适合的固体载体是例如滑石、二氧化钛、叶蜡石黏土、硅石、凹凸棒石黏土、硅藻土、石灰石、碳酸钙、膨润土、钙蒙脱土、棉籽壳、小麦粉、大豆粉、浮石、木粉、经研磨的胡桃壳、木质素和类似的物质。
许多表面活性物质可以有利地用在固体和液体配制品两者中,尤其是在使用前可被载体稀释的那些配制品中。表面活性物质可以是阴离子的、阳离子的、非离子的或聚合的并且它们可以用作乳化剂、湿润剂或悬浮剂或用于其他目的。典型的表面活性物质包括例如烷基硫酸酯的盐,如十二烷基硫酸二乙醇铵;烷基芳基磺酸酯的盐,如十二烷基苯磺酸钙;烷基酚/氧化烯加成产物,如乙氧基化壬基苯酚;醇/氧化烯加成产物,如乙氧基化十三烷醇;皂,如硬脂酸钠;烷基萘磺酸酯的盐,如二丁基萘磺酸钠;磺基琥珀酸二烷基酯的盐,如二(2-乙基己基)磺基琥珀酸钠;山梨糖醇酯,如山梨糖醇油酸酯;季铵,如氯化十二烷基三甲基铵;脂肪酸的聚乙二醇酯,如聚乙二醇硬脂酸酯;环氧乙烷和环氧丙烷的嵌段共聚物;以及磷酸单烷基酯和二烷基酯的盐;以及还有另外的物质,例如描述于:McCutcheon'sDetergents and Emulsifiers Annual[麦卡琴清洁剂和乳化剂年鉴],MC出版公司(MCPublishing Corp.),里奇伍德,新泽西州(Ridgewood New Jersey)(1981)。
可以用于杀有害生物配制品的另外的辅助剂包括结晶抑制剂、粘度改性剂、悬浮剂、染料、抗氧化剂、发泡剂、光吸收剂、混合助剂、消泡剂、络合剂、中和或改变pH的物质和缓冲液、腐蚀抑制剂、香料、湿润剂、吸收增强剂、微量营养素、增塑剂、助流剂、润滑剂、分散剂、增稠剂、防冻剂、杀微生物剂、以及液体和固体肥料。
根据本发明的配制品可以包括添加剂,该添加剂包括植物或动物来源的油、矿物油、此类油的烷基酯或此类油与油衍生物的混合物。在根据本发明的配制品中的油添加剂的量通常是基于该待施用的混合物的从0.01%到10%。例如,可以在喷雾混合物已经制备之后将该油添加剂以所希望的浓度添加到喷雾罐中。优选的油添加剂包括矿物油或植物来源的油,例如菜籽油、橄榄油或葵花籽油;乳化的植物油;植物来源的油的烷基酯,例如甲基衍生物;或动物来源的油,如鱼油或牛脂。优选的油添加剂包括C8-C22脂肪酸的烷基酯,尤其是C12-C18脂肪酸的甲基衍生物,例如月桂酸、棕榈酸以及油酸的甲基酯(分别为月桂酸甲酯、棕榈酸甲酯和油酸甲酯)。许多油衍生物获知于Compendium of Herbicide Adjuvants[除草剂辅助剂纲要],第10版,南伊利诺伊大学,2010。
这些配制品通常包含按重量计从0.1%到99%的,尤其是按重量计从0.1%到95%的组分(A)和组分(B)的化合物以及按重量计从1%到99.9%的配制辅助剂,该配制辅助剂优选地包括按重量计从0到25%的表面活性物质。而商业产品可以优选地被配制为浓缩物,最终使用者将通常使用稀释配制品。
施用比率在宽范围之内变化并且取决于土壤的性质、施用方法、作物植物、待控制的有害生物、主要气候条件、以及受施用方法、施用时间以及目标作物支配的其他因素。一般来讲,可以将化合物以从1l/ha至2000l/ha、尤其是从10l/ha到1000l/ha的比率施用。
包含以上描述的具有式(I)的化合物的某些混合物组合物可以示出协同效应。无论何时活性成分组合的作用大于单独组分的作用之和,这种协同效应发生。对于给定的活性成分组合,预期的作用E服从所谓的科尔比(COLBY)公式并且可以按以下进行计算(COLBY,S.R.“Calculating synergistic and antagonistic responses of herbicidecombination[计算除草剂组合的协同和拮抗反应]”.Weeds[杂草],第15卷,第20-22页;1967):
ppm=每升喷洒混合物的活性成分(=a.i.)的毫克数
X=使用p ppm的活性成分按活性成分A)计的%作用
Y=使用q ppm的活性成分按活性成分B)计的%作用。
根据科尔比,使用p+q ppm的活性成分,预期的(加性的)活性成分A)+B)的作用是:
如果实际观察到的作用(O)大于预期的作用(E),那么该组合的作用是超级加性的,即存在协同效应。在数学方面,协同作用对应于(O-E)的差的正值。在纯互补性添加活性物(期待的活性)的情况下,所述差(O-E)为零。所述差(O-E)的负值标志着与期待的活性相比,活性的损失。
然而,除了相对于杀真菌活性的实际协同作用外,根据本发明的组合物还可以具有另外的出人意料的有利特性。可以提及的此类有利的特性的实例是:更有利的降解性;改善的毒理学和/或生态毒理学行为;或有用植物的改善的特征,包括:出苗、作物产量、根系统更发达、分蘖增加、株高增加、叶片更大、基部叶片死亡更少、分蘖更强、叶子颜色更绿、所需肥料更少、所需种子更少、分蘖更多产、开花更早、谷粒成熟更早、植物倒伏(伏到(lodging))更少、芽生长增强、改善的植物活力以及发芽早。
根据本发明的组合物可以被施用至植物病原性微生物、有用植物、其场所、其繁殖材料、储存货物或受微生物攻击威胁的技术材料。
可以在有用植物、其繁殖材料、储存货物或技术材料被微生物感染之前或之后施用根据本发明的组合物。
要施用的根据本发明的组合物的量将取决于各种因素,如所使用的化合物;处理的对象,例如像植物、土壤或种子;处理的类型,例如像喷雾、洒粉或拌种;处理的目的,例如像预防或治疗;要控制的真菌类型或施用时间。
典型地,当典型地与1至5000g a.i./ha,特别是2至2000g a.i./ha,例如100ga.i./ha、250g a.i./ha、500g a.i./ha、800g a.i./ha、1000g a.i./ha、1500g a.i./ha的组分(B)组合施用至有用植物时,组分(A)典型地是以5至2000g a.i./ha,特别是10至1000ga.i./ha,例如50g a.i./ha、75g a.i./ha、100g a.i./ha或200g a.i./ha的比率施用的。
在农业实践中,根据本发明的组合物的施用比率取决于所希望的作用的类型,并且典型地是在从20至4000g的总组合物每公顷的范围内。
当根据本发明的组合物用于处理种子时,比率为0.001至50g组分(A)的化合物/每kg的种子、优选从0.01至10g/每kg的种子,以及0.001至50g的组分(B)的化合物/每kg的种子、优选从0.01至10g/每kg的种子,这一般是足够的。
为了避免疑问,在本申请的正文中引用文献参考、专利申请,或专利时,将所述引用的全文通过援引并入本文。
实例
接下来的实例用来说明本发明。
本发明的化合物(和组合物)与已知化合物(和组合物)的区别可以在于在低施用率下更大的效力,这可以由本领域的技术人员使用在实例中概述的实验程序,使用更低的施用率(如果必要的话)例如,50ppm、12.5ppm、6ppm、3ppm、1.5ppm或0.2ppm的一种或多种活性成分来证实。
贯穿本说明书,以摄氏度给出温度并且“m.p.”意指熔点。LC/MS意指液相色谱-质谱,并且装置和方法的描述如下:
方法G:
在来自沃特斯公司(Waters)的质谱仪(SQD、SQDII单四极杆质谱仪)上记录光谱,其装备有电喷射源(极性:正离子和负离子),毛细管电压:3.00kV,锥孔范围:30V,萃取器:2.00V,源温度:150℃,去溶剂化温度:350℃,锥孔气体流量:50l/h,去溶剂化气体流量:650L/h,质量范围:100Da至900Da)和来自沃特斯公司的Acquity UPLC:二元泵、经加热的柱室、二极管阵列检测器和ELSD检测器。柱:Waters UPLC HSS T3,1.8μm,30×2.1mm,温度:60℃,DAD波长范围(nm):210至500,溶剂梯度:A=水+5%MeOH+0.05%HCOOH,B=乙腈+0.05%HCOOH;梯度:10%-100%B,在1.2min内;流量(mL/min)0.85。
方法H:
在来自沃特斯公司(Waters)的质谱仪(SQD、SQDII单四极杆质谱仪)上记录光谱,其装备有电喷射源(极性:正离子和负离子),毛细管电压:3.00kV,锥孔范围:30V,萃取器:2.00V,源温度:150℃,去溶剂化温度:350℃,锥孔气体流量:50L/h,去溶剂化气体流量:650L/h,质量范围:100Da至900Da)和来自沃特斯公司的Acquity UPLC:二元泵、经加热的柱室、二极管阵列检测器和ELSD检测器。柱:Waters UPLC HSS T3,1.8μm,30×2.1mm,温度:60℃,DAD波长范围(nm):210至500,溶剂梯度:A=水+5%MeOH+0.05%HCOOH,B=乙腈+0.05%HCOOH;梯度:10%-100%B,在2.7min内;流量(mL/min)0.85。
必要时,在对映异构体意义上纯的最终化合物可以在适当时从外消旋材料经由标准物理分离技术(例如反相手性色谱法)或通过立体选择性合成技术(例如通过使用手性起始材料)获得。
配制品实例
将活性成分与辅助剂充分混合并且将混合物在合适的研磨机中充分研磨,从而提供可以用水稀释而给出所希望的浓度的悬浮液的可湿性粉剂。
将该活性成分与辅助剂充分混合并且将混合物在合适的研磨机中充分研磨,从而提供可以直接用于种子处理的粉剂。
可乳化浓缩物
在植物保护中可以使用的具有任何所要求的稀释的乳液可以通过用水稀释从这种浓缩物中获得。
通过将活性成分与载体混合并且将混合物在合适的研磨机中研磨而获得即用型尘粉剂。此类粉剂还可以用于种子的干拌种。
挤出机颗粒
将活性成分与辅助剂混合并且研磨,并且将混合物用水润湿。将混合物挤出并且然后在空气流中干燥。
包衣的颗粒
活性成分[组分(A)和(B)] 8%
聚乙二醇(分子量200) 3%
高岭土 89%
将精细研磨的活性成分在混合器中均匀地施用到用聚乙二醇润湿的高岭土上。以此方式获得无尘的包衣的颗粒。
悬浮液浓缩物
将精细研磨的活性成分与辅助剂密切地混合,得到悬浮液浓缩物,从该悬浮液浓缩物可以通过用水稀释获得任何所希望的稀释度的悬浮液。使用此类稀释物,可以对活的植物连同植物繁殖材料进行处理并且对其针对微生物侵染通过喷雾、浇灌或浸渍进行保护。
种子处理用的可流动性浓缩物
将精细研磨的活性成分与辅助剂密切地混合,得到悬浮液浓缩物,从该悬浮液浓缩物可以通过用水稀释获得任何所希望的稀释度的悬浮液。使用此类稀释物,可以对活的植物连同植物繁殖材料进行处理并且对其针对微生物侵染通过喷雾、浇灌或浸渍进行保护。
缓释的胶囊悬浮液
将28份的活性成分[组分(A)和(B)]的组合与2份的芳香族溶剂以及7份的甲苯二异氰酸酯/多亚甲基-聚苯基异氰酸酯-混合物(8:1)进行混合。将此混合物在1.2份的聚乙烯醇、0.05份的消泡剂以及51.6份的水的混合物中进行乳化直至达到所希望的粒度。向此乳液中添加在5.3份的水中的2.8份的1,6-己二胺混合物。将混合物搅拌直至聚合反应完成。将获得的胶囊悬浮液通过添加0.25份的增稠剂以及3份的分散剂进行稳定。该胶囊悬浮液配制品含有28%的活性成分。介质胶囊的直径是8-15微米。将所得配制品作为适用于此目的装置中的水性悬浮液施用到种子上。
缩写清单:
Aq. =水性
br s =宽单峰
℃ =摄氏度
DCM =二氯甲烷
dd =双二重峰
DMF =二甲基甲酰胺
DMSO =二甲基亚砜
DMSO-d6 =氘代二甲基亚砜
d =二重峰
EtOAc =乙酸乙酯
equiv. =当量
h =小时
M =摩尔
m =多重峰
min =分钟
MHz =兆赫兹
mp =熔点
Pd2(dba)3 =三(二亚苄基丙酮)二钯(0)
Pd(dppf)Cl2·DCM=[1,1′-双(二苯基膦基)二茂铁]二氯钯(II),DCM络合物
Pd(PPh3)2Cl2 =双(三苯基膦)钯(II)二氯化物
ppm =百万分率
RT =室温
Rt =保留时间
s =单峰
t =三重峰
THF =四氢呋喃
LC/MS =液相色谱法质谱法(上面给出了用于LC/MS分析的装置和方法的描述)
X-Phos Pd G2 =氯(2-二环己基膦基-2′,4′,6′-三异丙基-1,1′-联苯基)[2-(2′-氨基-1,1′-联苯基)]钯(II)
制备实例:
实例1:本实例说明了(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.04)的制备
步骤1:2-(5-溴-2-甲基-苯氧基)乙酸甲酯的制备
向室温下的5-溴-2-甲基苯酚(53.47mmol,10.00g)和2-溴乙酸甲酯(1.5当量,80.20mmol,12.27g,7.44mL)在四氢呋喃(0.5mol/L,106.9mL)中的溶液中添加碳酸钾(2当量,106.9mmol,14.78g),并将浅棕色悬浮液加热至65℃持续2h,然后冷却至室温过夜。将反应混合物用EtOAc稀释并且用水洗涤。将水相用EtOAc萃取,并且将总的合并的有机相用水、盐水洗涤,经Na2SO4干燥,过滤,并且在真空中浓缩,以得到呈棕色液体的2-(5-溴-2-甲基-苯氧基)乙酸甲酯(47.22mmol,15.89g,88%产率)。粗制油被残留的2-溴乙酸甲酯轻微污染,但不经进一步纯化直接用于下一步。
LCMS(方法H),Rt=1.59min,MS:(M+1)=259,261;1H NMR(400MHz,CDCl3)δppm2.25(s,3H)3.84(s,3H)4.66(s,2H)6.84(d,1H)7.05(m,2H)
步骤2:(Z)-2-(5-溴-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯的制备
第1部分:向在室温下在氩气下的2-(5-溴-2-甲基苯氧基)乙酸酯(20.8g,80.3mmol)和甲酸甲酯(6.0当量,482mmol,29.5g,30.5mL)在四氢呋喃(0.5mol/L,161mL)中溶液中分批添加甲醇钠(20当量,161mmol,9.13g)。反应轻微放热,并在室温水浴的帮助下保持在30℃以下。将反应混合物在室温下搅拌1h并通过缓慢添加NaHCO3饱和水溶液进行淬灭。将两相分离并且将水相用EtOAc萃取。将总的合并的有机层用NaHCO3饱和水溶液、盐水洗涤,用Na2SO4干燥,过滤并在真空中浓缩,以得到2-(5-溴-2-甲基-苯氧基)-3-羟基-丙-2-烯酸甲酯,其无需进一步纯化即可直接用于下一步。
LCMS(方法G),Rt=0.80和0.90min,MS:(M+1)=287,289
第2部分:向在室温下在氩气下的粗2-(5-溴-2-甲基-苯氧基)-3-羟基-丙-2-烯酸甲酯和硫酸二甲酯(1.2当量,93.2mmol,11.8g,8.8mL)在DMF(0.5mol/L,155mL)中的溶液中添加碳酸钾(1.5当量,117mmol,16.3g),并将反应混合物在室温搅拌2h。将反应混合物通过缓慢添加水进行淬灭,并且将混合物用EtOAc萃取。将总的合并的有机层用NaHCO3的饱和水溶液、盐水洗涤,用Na2SO4干燥,过滤并在真空中浓缩。将残余物通过快速色谱法(环己烷:EtOAc)纯化以得到呈灰白色固体的(Z)-2-(5-溴-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(59.6mmol,18.0g,75%产率)。
LCMS(方法G),Rt=1.02min,MS:(M+1)=301,303;1H NMR(400MHz,CDCl3)δppm2.31(s,3H)3.74(s,3H)3.91(s,3H)6.86(d,1H)7.05(m,2H)7.35(s,1H)
步骤3:(Z)-2-[5-(环己烯-1-基)-2-甲基-苯氧基]-3-甲氧基-丙-2-烯酸甲酯的
制备
向(Z)-2-(5-溴-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(203mg,0.67mmol,1.00当量)在1,4-二噁烷(6mL)和水(1mL)中的溶液中添加环己烯-1-基硼酸(93.4mg,0.74mmol,1.10当量)、磷酸钾(295mg,1.35mmol,2.00当量)和X Phos Pd G2(53.0mg,0.07mmol,0.10当量)。将反应混合物在100℃下搅拌15min并移去热源。内容物达到室温之后,用EtOAc和饱和NaHCO3水溶液稀释,然后用EtOAc萃取。将全部合并的有机级分用饱和NaHCO3水溶液和盐水洗涤,用Na2SO4干燥,过滤,并在真空中浓缩。将残余物通过快速色谱法(环己烷:EtOAc)纯化以得到呈无定形固体的(Z)-2-[5-(环己烯-1-基)-2-甲基-苯氧基]-3-甲氧基-丙-2-烯酸甲酯。
LC-MS(方法G),Rt=1.17min,MS:(M+H)=303;1H NMR(400MHz,CDCl3)δppm 7.36(s,1H),7.11(d,1H),6.96(dd,1H),6.77(d,1H),6.04(m,1H),3.90(s,3H),3.74(s,3H),2.36(m,5H),2.17-2.25(m,2H),1.74-1.83(m,2H),1.63-1.71(m,2H)。
步骤4:(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.04)的制备
向(Z)-2-[5-(环己烯-1-基)-2-甲基-苯氧基]-3-甲氧基-丙-2-烯酸甲酯(132mg,0.44mmol,1.00当量)在己烷(0.87mL)和EtOAc(2.18mL)中的溶液中添加钯/碳(23.2mg,0.01mmol,0.02当量)。将反应混合物在氢气气氛下搅拌2天。将反应混合物经硅藻土过滤并真空浓缩。将所得粗残余物通过快速色谱法(环己烷:EtOAc)纯化以得到呈白色固体的(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(mp:131℃-132℃)。
LC-MS(方法G),Rt=1.21min,MS:(M+H)=305;1H NMR(400MHz,CDCl3)δppm ppm7.35(s,1H),7.10(d,1H),6.79(dd,1H),6.58(d,1H),3.90(s,3H),3.74(s,3H),2.38-2.47(m,1H),2.34(s,3H),1.80-1.89(m,4H),1.75(br,1H),1.33-1.42(m,4H),1.22-1.32(m,1H)。
实例2:本实例说明了(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(化合物X.02)的制备
在氩气气氛下,将氯化锌的1M THF溶液(2.54mmol)添加到环戊基溴化镁的2M THF溶液(2.54mmol)中,并在室温下搅拌浅黄色悬浮液10min,在此期间观察到小的放热。此后,添加(Z)-2-(5-溴-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯(0.153g,0.51mmol)在四氢呋喃(2.5mL)中的溶液和PdCl2(dppf)(0.19g,0.025mmol)并将浅黄色悬浮液在50℃下加热3小时。然后使反应混合物达到室温,用饱和NH4Cl水溶液淬灭,并用甲基叔丁基醚萃取。然后将总的合并的有机部分用水和盐水洗涤,经硫酸钠干燥,过滤并在减压下浓缩。将所得粗残余物通过快速色谱法(环己烷:EtOAc梯度)纯化以得到0.106mg呈白色固体的标题化合物(mp 80℃-83℃)。
LC-MS(方法G),Rt=1.16min,MS:(M+H)=291;1H NMR(400MHz,CDCl3)δppm:7.35(s,1H),7.09(d,1H),6.82(d,1H),6.60(s,1H),3.90(s,3H),3.72(s,3H),2.91(m,1H),2.32(s,3H),2.10-1.97(m,2H),1.85-1.75(m,2H),1.74-1.65(m,2H),1.60-1.45(m,2H)。
相应地可以使用上述以及下述的合成技术制备具有式(I)的化合物。
必要时,在对映异构体意义上纯的最终化合物可以在适当时从外消旋材料经由标准物理分离技术(例如反相手性色谱法)或通过立体选择性合成技术(例如通过使用手性起始材料)获得)。
表T1:根据式(I)的化合物X.01至X.04的熔点(mp)数据和/或保留时间(Rt):
生物学实例:
在孔板中叶圆片测试的一般实例:
从生长于温室中的植物上切割不同植物物种的叶圆片或叶段。将切割的叶圆片或叶段置于多孔板(24孔规格)中的水琼脂上。在接种之前(预防性)或之后(治疗性),将叶圆片用测试溶液喷雾。将待测试的化合物制备成DMSO溶液(最大10mg/mL),将其在就要喷雾之前用0.025%Tween20稀释至适当浓度。根据对应的测试系统,在限定的条件(温度、相对湿度、光等)下温育接种的叶圆片或叶段。取决于病害系统,接种后3至14天,进行病害水平的单评估。然后计算相对于未处理的检验叶圆片或叶段的病害控制百分比。
在孔板中液体培养测试的一般实例:
将真菌的菌丝体片段或分生孢子悬浮液(从所述真菌的液体培养物或从低温储存物新鲜制备)直接混入营养肉汤中。将测试化合物的DMSO溶液(最大10mg/mL)用0.025%的Tween20稀释50倍,并且将10μl的此溶液用移液管移取到微量滴定板(96孔规格)中。然后将含有真菌孢子/菌丝体片段的营养肉汤添加到其中,以得到测试化合物的终浓度。将测试板在24℃和96%相对湿度的黑暗中进行温育。取决于病害系统,2至7天之后光度测定地确定真菌生长的抑制,并且计算相对于未处理的检验物而言的抗真菌活性百分比。
实例A1:针对小麦隐匿柄锈菌(Puccinia recondita f.sp.tritici)的杀真菌活 性/小麦/叶圆片预防法(褐锈病)
将小麦叶段置于多孔板(24孔规格)中的琼脂上并且用测试溶液进行喷雾。干燥之后,将叶段用真菌的孢子悬浮液接种。适当的温育之后,化合物的活性8dpi(温育之后的天数)被评定为预防性杀真菌活性。
当与在相同条件下显示出广泛的病害发展的未处理的对照相比时,以下化合物在200ppm下对小麦隐匿柄锈菌给出至少80%的控制:
化合物(来自表T1):X.01、X.02、X.03、X.04
实例A2:针对小麦隐匿柄锈菌的杀真菌活性/小麦/叶圆片治疗法(褐锈病)
将小麦叶段置于多孔板(24孔规格)中的琼脂上。将叶段用真菌的孢子悬浮液接种,并在接种之后1天用测试溶液进行喷雾。适当的温育之后,化合物的活性8dpi(温育之后的天数)被评定为治疗性杀真菌活性。
当与在相同条件下显示出广泛的病害发展的未处理的对照相比时,以下化合物在200ppm下对小麦隐匿柄锈菌给出至少80%的控制:
化合物(来自表T1):X.01、X.02、X.04
实例A3:针对豆薯层锈菌的杀真菌活性/大豆/叶圆片预防法(亚洲大豆锈病)
将大豆叶圆片置于多孔板(24孔规格)中的琼脂上并且用测试溶液进行喷雾。干燥之后,将叶圆片用真菌的孢子悬浮液接种。适当的温育之后,化合物的活性约12dpi(温育之后的天数)被评定为预防性杀真菌活性。
当与在相同条件下显示出广泛的病害发展的未处理的对照相比时,以下化合物在60ppm下给出对豆薯层锈菌的至少70%的控制:
化合物(来自表T1):X.01、X.02、X.03、X.04
实例A4:针对瓜小丛壳菌(Glomerella lagenarium)(瓜类炭疽菌
(Colletotrichum lagenarium))液体培养物的杀真菌活性/黄瓜/预防法(炭疽病)
将来自冷冻储存的真菌分生孢子直接混入营养肉汤(PDB马铃薯右旋糖肉汤)中。将测试化合物的DMSO溶液置于微量滴定板(96孔规格)中并且向其中添加包含真菌孢子的营养肉汤。将这些测试板在24℃下温育并且在72小时之后在620nm下光度测定地确定对生长的抑制。
当与在相同条件下显示出广泛的病害发展的未处理的对照相比时,以下化合物在20ppm下对瓜小丛壳菌给出至少80%的控制:
化合物(来自表T1):X.01、X.02、X.03、X.04
对比数据:
将本发明的化合物X.02和X.04的生物活性与参考化合物Z-1和Z-2进行比较。参考化合物Z-1和Z-2分别具体披露于WO 98/03464的第16页和EP 0 212 859的第6页。
实例B:对抗小麦隐匿柄锈菌(褐锈病)的对比生物活性,治疗性的:
方法:将小麦叶段置于多孔板(24孔规格)中的琼脂上。将叶段用真菌的孢子悬浮液接种,并在接种之后1天用测试溶液进行喷雾。适当的温育之后,化合物的活性8dpi(温育之后的天数)被评定为治疗性杀真菌活性。
数据表示为下表B1中所述的生物学测试中每种化合物的病害控制百分比和测试率。
表B1-对抗小麦隐匿柄锈菌(褐锈病)的生物活性,治疗性的:
涉及包含组分(A)和(B)的混合物作为活性成分的杀真菌组合物的另外的生物测试实例:
实例C1针对落花生球腔菌(Mycosphaerella arachidis)又名花生褐斑病菌
(Cercospora arachidicola)(褐色叶斑病)的杀真菌活性
将来自冷冻储存的真菌分生孢子直接混入营养肉汤(PDB马铃薯右旋糖肉汤)中。将测试化合物的DMSO溶液置于微量滴定板(96孔规格)中并且向其中添加包含真菌孢子的营养肉汤。将这些测试板在24℃下温育并且在大约5-6天之后在620nm下光度测定地确定对生长的抑制。
当与在相同条件下显示出广泛的病害发展的未处理的对照相比时,以下化合物混合物在表中列举的比率下对落花生球腔菌(Mycosphaerella arachidis)给出至少80%的控制:
表C1-1-针对落花生球腔菌(Mycosphaerella arachidis)的杀真菌活性>80%(未 处理的%)
表C1-2-针对落花生球腔菌(Mycosphaerella arachidis)的杀真菌活性>80%(未 处理的%)
在该测试(落花生球腔菌(Mycosphaerella arachidis)又名花生褐斑病菌(Cercospora arachidicola)(花生褐色叶斑病))中,以下混合物组合物在表C1-3和C1-4中的报道的浓度(以ppm计)下给出以下病害控制。杀真菌活性以100-0等级(100=无病害增长;0=完全被菌丝体覆盖)进行评估。
表C1-3
表C1-4
实例C2-针对小麦壳针孢(叶疱斑症)的杀真菌活性
将来自冷冻储存的真菌分生孢子直接混入营养肉汤(PDB马铃薯右旋糖肉汤)中。将测试化合物的DMSO溶液置于微量滴定板(96孔规格)中并且向其中添加包含真菌孢子的营养肉汤。将这些测试板在24℃下温育并且在72小时之后光度测定地确定对生长的抑制。
当与在相同条件下显示出广泛的病害发展的未处理的对照相比时,以下化合物混合物在表中列举的比率下对小麦壳针孢给出至少80%的控制。
表C2-1-针对小麦壳针孢的杀真菌活性>80%(未处理的%)
表C2-2-针对小麦壳针孢的杀真菌活性>80%(未处理的%)
在该测试(小麦壳针孢(叶疱斑症))中,以下混合物组合物在表C2-3至C2-5中的报道的浓度(以ppm计)下给出以下病害控制。杀真菌活性以100-0等级(100=无病害增长;0=完全被菌丝体覆盖)进行评估。
表C2-3
表C2-4
表C2-5
实例C3-针对大豆壳针孢(Septoria glycines)(褐斑病)的杀真菌活性:
将从人工介质上生长的新鲜培养物收获的真菌分生孢子直接混入营养肉汤(PDB马铃薯右旋糖肉汤)中。将测试化合物的DMSO溶液置于微量滴定板(96孔规格)中并且向其中添加包含真菌孢子的营养肉汤。将这些测试板在24℃下温育并且在72小时之后光度测定地确定对生长的抑制。
当与在相同条件下显示出广泛的病害发展的未处理的对照相比时,以下化合物混合物在表中列举的比率下对大豆壳针孢(Septoria glycines)给出至少80%的控制:
表C3-1-针对大豆壳针孢(Septoria glycines)的杀真菌活性>80%(未处理的%)
表C3-2-针对大豆壳针孢(Septoria glycines)的杀真菌活性>80%(未处理的%)
在该测试(大豆壳针孢(Septoria glycines)(褐斑病))中,以下混合物组合物在表C3-3至C3-5中的报道的浓度(以ppm计)下给出以下病害控制。杀真菌活性以100-0等级(100=无病害增长;0=完全被菌丝体覆盖)进行评估。
表C3-3
表C3-4
表C3-5
实例C4-针对瓜小丛壳菌(Glomerella lagenarium)又名瓜类炭疽菌
(Colletotrichum lagenarium)(炭疽病)的杀真菌活性:
将来自冷冻储存的真菌分生孢子直接混入营养肉汤(PDB马铃薯右旋糖肉汤)中。将测试化合物的DMSO溶液置于微量滴定板(96孔规格)中并且向其中添加包含真菌孢子的营养肉汤。将这些测试板在24℃下温育并且在72小时之后在620nm下光度测定地确定对生长的抑制。
当与在相同条件下显示出广泛的病害发展的未处理的对照相比时,以下化合物混合物在表中列举的比率下对瓜小丛壳菌(Glomerella lagenarium)给出至少80%的控制:
表C4-1-针对瓜小丛壳菌(Glomerella lagenarium)的杀真菌活性>80%(未处理 的%)
表C4-2-针对瓜小丛壳菌(Glomerella lagenarium)的杀真菌活性>80%(未处理 的%)
在该测试(瓜小丛壳菌(Glomerella lagenarium)又名瓜类炭疽菌 (Colletotrichum lagenarium))中,以下混合物组合物在表C4-3和C4-4中的报道的浓度(以ppm计)下给出以下病害控制。杀真菌活性以100-0等级(100=无病害增长;0=完全被菌丝体覆盖)进行评估。
表C4-3
表C4-4
实例C5-针对多主棒孢菌(靶叶斑病)的杀真菌活性
将来自冷冻储存的真菌分生孢子直接混入营养肉汤(PDB马铃薯右旋糖肉汤)中。将测试化合物的DMSO溶液置于微量滴定板(96孔规格)中并且向其中添加包含真菌孢子的营养肉汤。将这些测试板在24C下温育并且在3-4天之后在620nm下光度测定地确定对生长的抑制。
在该测试(多主棒孢菌)中,以下混合物组合物在表C4-3和C4-4中的报道的浓度(以ppm计)下给出以下病害控制。杀真菌活性以100-0等级(100=无病害增长;0=完全被菌丝体覆盖)进行评估。
表C5-1
实例D:针对大豆上的豆薯层锈菌的预防性活性
种植之后4周,将整株大豆植物用所描述的活性成分处理。喷雾之后1天,从第一片具三叶的叶片切割叶圆片。在各比率下进行五次重复。在处理之后一天,将叶圆片用豆薯层锈菌(亚洲大豆锈菌)接种。在接种之后11至14天,对叶圆片进行评估,并且活性来源于处理与未处理的侵染检验的关系(100=无病害、对叶片无损害,0=高度侵染、叶片损害严重)。使用的活性成分的比率以g活性成分(a.i.)/ha在表中给出。
结果示于下表中:
表D1-针对豆薯层锈菌的活性(未处理的%)
表D2-针对豆薯层锈菌的活性(未处理的%)
表D3-针对豆薯层锈菌的活性(未处理的%)
表D4-针对豆薯层锈菌的活性(未处理的%)
表D5-针对豆薯层锈菌的活性(未处理的%)
表D6-针对豆薯层锈菌的活性(未处理的%)
表D7-针对豆薯层锈菌的活性(未处理的%)
表D8-针对豆薯层锈菌的活性(未处理的%)
表D9-针对豆薯层锈菌的活性(未处理的%)
表D10-针对豆薯层锈菌的活性(未处理的%)
表D11-针对豆薯层锈菌的活性(未处理的%)
表D12-针对豆薯层锈菌的活性(未处理的%)
表D13-针对豆薯层锈菌的活性(未处理的%)
表D14-针对豆薯层锈菌的活性(未处理的%)
表D15-针对豆薯层锈菌的活性(未处理的%)
表D16-针对豆薯层锈菌的活性(未处理的%)
表D17-针对豆薯层锈菌的活性(未处理的%)
表D18-针对豆薯层锈菌的活性(未处理的%)
表D19-针对豆薯层锈菌的活性(未处理的%)
表D20-针对豆薯层锈菌的活性(未处理的%)
表D21-针对豆薯层锈菌的活性(未处理的%)
表D22-针对豆薯层锈菌的活性(未处理的%)
表D23-针对豆薯层锈菌的活性(未处理的%)
表D24-针对豆薯层锈菌的活性(未处理的%)
表D25-针对豆薯层锈菌的活性(未处理的%)
表D26-针对豆薯层锈菌的活性(未处理的%)
表D27-针对豆薯层锈菌的活性(未处理的%)
Claims (15)
1.一种杀真菌组合物,所述杀真菌组合物包含作为活性成分的组分(A)和(B)的混合物,其中组分(A)是具有式(I)的化合物:
其中
R1是甲基;
R2是氢;
R3是氢;
R4是C3-C7环烷基;
或其农艺学上可接受的盐;
并且
组分(B)是选自由以下组成的组的化合物:
联苯吡菌胺、硫、氢氧化铜、氯啶菌酯、阿拉酸式苯-S-甲基、王铜、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、多效唑、丙硫菌唑、咪鲜胺、丙环唑、啶菌噁唑、戊唑醇、苯锈啶、丁苯吗啉、螺环菌胺、嘧菌环胺、咯菌腈、甲霜灵、甲霜灵-M、多菌灵、吡噻菌胺、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、灭菌丹、百菌清、氟啶胺、氟唑菌酰胺、环酰菌胺、三乙膦酸铝、吡菌苯威、三环唑、双炔酰菌胺、氟苯醚酰胺、吡唑萘菌胺、氟唑环菌胺、苯并烯氟菌唑、氟唑菌酰羟胺、异氟普兰、异噻菌胺、地芬灭替松、氟茚唑菌胺、甲香菌酯、鲁本米西安、曼德斯宾、氟噻唑吡乙酮、联苯吡嗪菌胺、英派尔福沙姆、氯氟醚菌唑、异芬特氟克那唑、爱米诺庇力芬、(Z,2E)-5-[1-(4-氯苯基)吡唑-3-基]氧基-2-甲氧基亚氨基-N,3-二甲基-戊-3-烯酰胺、吡啶菌酰胺、芬庇科米得、氟苯喹、奎诺福林、苯噻菌酯、氟吡菌酰胺、吡丙炔、2-(二氟甲基)-N-(3-乙基-1,1-二甲基-茚满-4-基)吡啶-3-甲酰胺、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈、美特尔特特拉普罗、氟哌啶、烯肟菌酯、4-[[6-[2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(5-硫代-4H-1,2,4-三唑-1-基)丙基]-3-吡啶基]氧基]苯甲腈、抗倒酸、抗倒酯、丁香菌酯、N'-[5-溴-2-甲基-6-[(1S)-1-甲基-2-丙氧基-乙氧基]-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-[(1R)-1-甲基-2-丙氧基-乙氧基]-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-氯-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-异丙基-N-甲基-甲脒、N'-[5-溴-2-甲基-6-(2-丙氧基丙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒、N-异丙基-N’-[5-甲氧基-2-甲基-4-(2,2,2-三氟-1-羟基-1-苯基-乙基)苯基]-N-甲基-甲脒、N’-[4-(1-环丙基-2,2,2-三氟-1-羟基-乙基)-5-甲氧基-2-甲基-苯基]-N-异丙基-N-甲基-甲脒、N-乙基-N’-[5-甲氧基-2-甲基-4-[2-三氟甲基)氧杂环丁烷-2-基]苯基]-N-甲基-甲脒、N-乙基-N’-[5-甲氧基-2-甲基-4-[2-三氟甲基)四氢呋喃-2-基]苯基]-N-甲基-甲脒、N-(2-氟苯基)-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、N-甲氧基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]环丙烷甲酰胺、N,2-二甲氧基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、N-乙基-2-甲基-N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、[(1S,2S)-1-甲基-2-(邻甲苯基)丙基](2S)-2-[(4-甲氧基-3-丙酰基氧基-吡啶-2-羰基)氨基]丙酸酯、1-甲氧基-3-甲基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、1,3-二甲氧基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、3-乙基-1-甲氧基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]脲、N-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]丙酰胺、4,4-二甲基-2-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]异噁唑烷-3-酮、5,5-二甲基-2-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]异噁唑烷-3-酮、1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]吡唑-4-甲酸乙酯、N,N-二甲基-1-[[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲基]-1,2,4-三唑-3-胺、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈、3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈、2-氨基-6-甲基-吡啶-3-甲酸(4-苯氧基苯基)甲酯、N-甲基-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]硫代苯甲酰胺;N-甲基-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺;(Z,2E)-5-[1-(2,4-二氯苯基)吡唑-3-基]氧基-2-甲氧基亚氨基-N,3-二甲基-戊-3-烯酰胺、(5-甲基-2-吡啶基)-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲酮、(3-甲基异噁唑-5-基)-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]甲酮、1-[[5-[5-(三氟甲基)-1,2,4-噁二唑-3-基]-2-噻吩基]甲基]吡唑-4-甲酸乙酯、2,2-二氟-N-甲基-2-[4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯基]乙酰胺、N-[(Z)-甲氧基亚氨基甲基]-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、N-[N-甲氧基-C-甲基-碳酰亚胺基]-4-[5-(三氟甲基)-1,2,4-噁二唑-3-基]苯甲酰胺、N-[3-(4-氯苯基)-4,5-二氢异噁唑-5-基]-5-甲基-1,2,4-噁二唑-3-甲酰胺、2-(二氟甲基)-N-(1,1-二甲基-3-丙基-茚满-4-基)吡啶-3-甲酰胺、[(1S,2S)-2-(4-氟-2-甲基-苯基)-1,3-二甲基-丁基](2S)-2-[(3-乙酰氧基-4-甲氧基-吡啶-2-羰基)氨基]丙酸酯、[(1S,2S)-2-(4-氟-2-甲基-苯基)-1,3-二甲基-丁基](2S)-2-[[3-(乙酰氧基甲氧基)-4-甲氧基-吡啶-2-羰基]氨基]丙酸酯、顺式-茉莉酮、膦酸钾、膦酸钙、草甘膦、2,4-D、麦草畏、草铵膦、噻虫嗪、环丁氟仑、异噁唑虫酰胺、甲氧哌啶乙酯、阿维菌素、埃玛菌素、溴氰虫酰胺、氯虫苯甲酰胺、丁醚脲、溴虫氟苯双酰胺、2-氯-N-环丙基-5-(1-{2,6-二氯-4-[1,2,2,2-四氟-1-(三氟甲基)乙基]苯基}-1H-吡唑-4-基)-N-甲基烟酰胺和氟噁唑酰胺。
2.根据权利要求1所述的杀真菌组合物,其中,组分(A)是选自以下的化合物:
(Z)-2-(5-环丁基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯
(化合物X.01),
(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯
(化合物X.02),
(Z)-2-(5-环丙基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯
(化合物X.03),或
(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯
(化合物X.04);
或其农艺学上可接受的盐。
3.根据权利要求1或权利要求2所述的杀真菌组合物,其中,组分(A)是:
(Z)-2-(5-环戊基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯
(化合物X.02),或
(Z)-2-(5-环己基-2-甲基-苯氧基)-3-甲氧基-丙-2-烯酸甲酯
(化合物X.04);
或其农艺学上可接受的盐。
4.根据权利要求1至3中任一项所述的杀真菌组合物,其中,组分(B)是选自由以下组成的组的化合物:联苯吡菌胺、氯啶菌酯、环唑醇、苯醚甲环唑、氟环唑、粉唑醇、己唑醇、种菌唑、叶菌唑、丙硫菌唑、丙环唑、戊唑醇、嘧菌酯、醚菌胺、烯肟菌胺、氟菌螨酯、氟嘧菌酯、苯氧菌胺、肟菌酯、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、代森锰锌、百菌清、氟唑菌酰胺、吡菌苯威、苯并烯氟菌唑、异氟普兰、甲香菌酯、曼德斯宾、氯氟醚菌唑、异芬特氟克那唑、苯噻菌酯、美特尔特特拉普罗、烯肟菌酯、丁香菌酯、2-[6-(4-氯苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、2-[6-(4-溴苯氧基)-2-(三氟甲基)-3-吡啶基]-1-(1,2,4-三唑-1-基)丙-2-醇、3-[2-(1-氯环丙基)-3-(2-氟苯基)-2-羟基-丙基]咪唑-4-甲腈和3-[2-(1-氯环丙基)-3-(3-氯-2-氟-苯基)-2-羟基-丙基]咪唑-4-甲腈。
5.根据权利要求1至4中任一项所述的杀真菌组合物,其中,组分(B)是选自由以下组成的组的化合物:环唑醇、苯醚甲环唑、己唑醇、丙硫菌唑、丙环唑、嘧菌酯、肟菌酯、啶氧菌酯、唑菌胺酯、代森锰锌、百菌清、氟唑菌酰胺、苯并烯氟菌唑、异氟普兰和美特尔特特拉普罗。
6.根据权利要求1至5中任一项所述的杀真菌组合物,其中,组分(B)是嘧菌酯或肟菌酯。
7.根据权利要求1至6中任一项所述的杀真菌组合物,其中,组分(A)与组分(B)的重量比是从100:1至1:100。
8.根据权利要求1至7中任一项所述的杀真菌组合物,其中,该组分(A)与组分(B)的重量比是从20:1至1:40。
9.根据权利要求1至8中任一项所述的杀真菌组合物,其中,该组分(A)与组分(B)的重量比是从12:1至1:25。
10.根据权利要求1至9中任一项所述的杀真菌组合物,其中,该组分(A)与组分(B)的重量比是从5:1和1:15。
11.根据权利要求1至10中任一项所述的杀真菌组合物,其中,该组分(A)与组分(B)的重量比是从2:1至1:5。
12.根据权利要求1至11中任一项所述的杀真菌组合物,其中,所述组合物包含一种或多种另外的杀有害生物剂,所述杀有害生物剂选自由以下组成的组:
杀真菌剂,所述杀真菌剂选自土菌灵、氟啶胺、苯并烯氟菌唑、氟唑菌酰羟胺、苯霜灵、苯霜灵-M(精苯霜灵)、呋霜灵、甲霜灵、甲霜灵-M(精甲霜灵)、多地辛、N'-(2,5-二甲基-4-苯氧基-苯基)-N-乙基-N-甲基-甲脒、N'-[4-(4,5-二氯-噻唑-2-基氧基)-2,5-二甲基-苯基]-N-乙基-N-甲基-甲脒、N'-[4-[[3-[(4-氯苯基)甲基]-1,2,4-噻二唑-5-基]氧基]-2,5-二甲基-苯基]-N-乙基-N-甲基-甲脒、乙菌定、3'-氯-2-甲氧基-N-[(3RS)-四氢-2-氧代呋喃-3-基]乙酰-2',6'-二甲基苯胺(抑霉胺)、嘧菌环胺、嘧菌胺、嘧霉胺、二噻农、金色制霉素、杀稻瘟菌素-S、联苯、地茂散、氯硝铵、六氯苯、五氯硝基苯、四氯硝基苯(TCNB)、甲基立枯磷、苯菌酮、2,6-二氯-N-(4-三氟甲基苄基)-苯甲酰胺、氟吡菌胺、硫氰苯甲酰胺、磺菌胺、苯菌灵、多菌灵、多菌灵盐酸盐、氯芬唑、麦穗宁、噻苯咪唑、甲基硫菌灵、苯噻菌胺、灭瘟唑、噻菌灵、阿拉酸式苯、百杀辛、甲氧苯唳菌(IKF-309)、阿拉酸式苯-S-甲基、吡菌苯威(KIF-7767)、丁胺、3-碘-2-丙炔基正丁基氨基甲酸酯(IPBC)、碘代丙炔基丁基氨基甲酸酯(异丙烷基丁基氨基甲酸酯)、异丙烷基丁基氨基甲酸酯(碘代丙炔基丁基氨基甲酸酯)、四唑吡氨酯、聚氨基甲酸酯、霜霉威、三氟甲氧威、3-(二氟甲基)-N-(7-氟-1,1,3,3-四甲基-茚满-4-基)-1-甲基-吡唑-4-甲酰胺、双氯氰菌胺、N-[(5-氯-2-异丙基-苯基)甲基]-N-环丙基-3-(二氟甲基)-5-氟-1-甲基-吡唑-4-甲酰胺、N-环丙基-3-(二氟甲基)-5-氟-N-[(2-异丙基苯基)甲基]-1-甲基-吡唑-4-甲酰胺、环丙酰菌胺、百菌清、氟吗啉、喹啉铜、霜脲氰、氰烯菌酯、氰霜唑、氟噻唑菌腈、噻菌腈、乙菌利、异菌脲、腐霉利、农利灵、磺酸丁嘧啶、邻敌螨消、硝戊酯、消螨通、敌螨普、消螨多、二苯胺、氯瘟磷、2,6-二甲基-[1,4]二噻英并[2,3-c:5,6-c']二吡咯-1,3,5,7(2H,6H)-四酮、氧化福美双、代森硫、福美铁、代森锰锌、代森锰、威百亩、代森联、代森联-锌、代森钠、甲基代森锌、福美双、硫威钠、代森锌、福美锌、二甲基二硫醚、稻瘟灵、噻唑菌胺、三乙膦酸、三乙膦酸铝(疫霜灵)、溴甲烷、碘甲烷、异硫氰酸甲酯、环菌胺、甲呋酰胺、有效霉素、链霉素、(2RS)-2-溴-2-(溴甲基)戊二腈(溴菌腈)、多果定、十二烷基胍醋酸盐、双胍辛盐、双胍辛胺、双胍辛胺三乙酸盐、2,4-D、2,4-DB、春日霉素、甲菌定、环酰菌胺、恶霉灵、土菌消、抑霉唑、抑霉唑硫酸盐、恶咪唑、稻瘟酯、咪鲜胺、氟菌唑、咪唑菌酮、波尔多混合剂、多硫化钙、乙酸铜、碳酸铜、氢氧化铜、环烷酸铜、油酸铜、王铜、羟基喹啉铜、硅酸铜、硫酸铜、妥尔铜、氧化亚铜、硫、西维因、稻瘟酞(四氯苯酞)、啶菌噁唑(菌思奇)、氟噻唑吡乙酮、氟里醚、双炔酰菌胺、KSF-1002、抑菌啉、烯酰吗啉、丁苯吗啉、十三吗啉、十二环吗啉、乙霉威、三苯基乙酸锡、三苯基氢氧化锡、萎锈灵、氧化萎锈灵、敌菌酮、噁唑菌酮、间-苯基苯酚、对-苯基苯酚、三溴苯酚(TBP)、2-[2-[(7,8-二氟-2-甲基-3-喹啉基)氧基]-6-氟-苯基]丙烷-2-醇、2-[2-氟-6-[(8-氟-2-甲基-3-喹啉基)氧基]苯基]丙烷-2-醇、环氟菌胺、呋酰胺、恶霜灵、氟酰胺、灭锈胺、异丙噻菌胺、拌种咯、咯菌腈、戊菌隆、克瘟散、异稻瘟净、定菌磷、磷酸、叶枯酞、敌菌丹、克菌丹、灭菌磷、嗪氨灵、苯锈啶、粉病灵、蛇床子素、1-甲基环丙烯、4-CPA、矮壮素、苯哒嗪酸、2,4-滴丙酸、噻节因、茵多酸、乙烯利、氟节胺、氯吡脲、赤霉酸、赤霉素、恶霉灵、马来酰肼、助壮素、萘乙酰胺、多效唑、调环酸、调环酸钙、噻苯隆、脱叶磷(三硫代磷酸三丁酯)、抗倒酸、烯效唑、α-萘乙酸、多氧菌素D(多抗霉素)、BLAD、壳聚糖、氰菌胺、灭菌丹、3-(二氟甲基)-N-甲氧基-1-甲基-N-[1-甲基-2-(2,4,6-三氯苯基)乙基]吡唑-4-甲酰胺、联苯吡菌胺、氟唑菌酰胺、呋吡菌胺、吡唑萘菌胺、戊苯吡菌胺、吡噻菌胺、氟唑环菌胺、胺苯吡菌酮、哒菌酮、啶斑肟、啶酰菌胺、氟吡菌酰胺、二氟林、氯苯嘧啶醇、5-氟-2-(对-甲苯基甲氧基)嘧啶-4-胺、嘧菌腙、菌核净、咯喹酮、丙氧喹啉、乙氧喹、喹氧灵、4,4,5-三氟-3,3-二甲基-1-(3-喹啉基)异喹啉、4,4-二氟-3,3-二甲基-1-(3-喹啉基)异喹啉、5-氟-3,3,4,4-四甲基-1-(3-喹啉基)异喹啉、9-氟-2,2-二甲基-5-(3-喹啉基)-3H-1,4-苯并氧杂吖庚因、异丁乙氧喹啉、噁喹酸、灭螨猛、螺环菌胺、(E)-N-甲基-2-[2-(2,5-二甲基苯氧基甲基)苯基]-2-甲氧基-亚氨基乙酰胺、(曼德斯宾)、嘧菌酯、丁香菌酯、醚菌胺、烯肟菌酯、吡洛特宾、烯肟菌胺、氟菌螨酯、氟嘧菌酯、醚菌酯、曼德斯宾、苯氧菌胺、叉氨苯酰胺、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、氯啶菌酯、肟菌酯、吲唑磺菌胺、抑菌灵、对甲抑菌灵、丁-3-炔基N-[6-[[(Z)-[(1-甲基四唑-5-基)-苯基-亚甲基]氨基]氧基甲基]-2-吡啶基]氨基甲酸酯、棉隆、异噻菌胺、噻酰菌胺、噻呋酰胺、苯噻硫氰(TCMTB)、硫硅菌胺、苯酰菌胺、防霉灵、三环唑、(.+-.)-顺式-1-(4-氯苯基)-2-(1H-1,2,4-三唑-1-基)-环庚醇(环菌唑)、1-(5-溴-2-吡啶基)-2-(2,4-二氟苯基)-1,1-二氟-3-(1,2,4-三唑-1-基)丙烷-2-醇、2-(1-叔丁基)-1-(2-氯苯基)-3-(1,2,4-三唑-1-基)-丙烷-2-醇(TCDP)、(N'-[5-溴-2-甲基-6-(1-甲基-2-丙氧基-乙氧基)-3-吡啶基]-N-乙基-N-甲基-甲脒)、阿扎康唑、联苯三唑醇(双苯三唑醇)、糠菌唑、氯咪巴唑、环唑醇、苯醚甲环唑、地美康唑、烯唑醇、烯唑醇-M、氟环唑、乙环唑、腈苯唑、氟喹唑、氟硅唑、粉唑醇、己唑醇、亚胺唑、种菌唑、叶菌唑、腈菌唑、戊菌唑、丙环唑、丙硫菌唑、氯氟醚菌唑、硅氟唑、戊唑醇、四氟醚唑、三唑酮、三唑醇、咪唑嗪、灭菌唑、2-[[(1R,5S)-5-[(4-氟苯基)甲基]-1-羟基-2,2-二甲基-环戊基]甲基]-4H-1,2,4-三唑-3-硫酮、2-[[3-(2-氯苯基)-2-(2,4-二氟苯基)环氧乙烷-2-基]甲基]-4H-1,2,4-三唑-3-硫酮、唑嘧菌胺、异丙菌胺、缬菌胺、2-苄基-4-氯酚(苄氯酚)、烯丙醇、唑啶草酮、苯扎氯铵、氯化苦、甲酚、达拉赛得、二氯芬(双氯酚)、燕麦枯、双硫氧吡啶、N-(2-对氯苯甲酰基乙基)-六亚甲基四胺氯化物、NNF-0721、辛噻酮、环氧嘧磺隆、包含茶树油互生叶白千层的植物提取物(Timorex GoldTM)、包含有机碳、营养素和氨基酸的生物刺激素(QuantisTM)、丙烷脒以及丙酸;或者
杀昆虫剂,所述杀昆虫剂选自阿维菌素、高灭磷、啶虫脒、磺胺螨酯(S-1955)、阿弗麦菌素、印楝素、甲基谷硫磷、联苯菊酯、联苯肼酯、溴虫氟苯双酰胺、噻嗪酮、克百威、巴丹、氯虫苯甲酰胺(DPX-E2Y45)、溴虫腈、氟啶脲、毒死蜱、甲基毒死蜱、环虫酰肼、噻虫胺、丁氟螨酯、氟氯氰菊酯、β-氟氯氰菊酯、三氟氯氰菊酯、λ-三氯氟氰菊酯、氯氰菊酯、灭蝇胺、溴氰菊酯、丁醚脲、二嗪农、狄氏剂、除虫脲、四氟甲醚菊酯、乐果、呋虫胺、苯虫醚、埃玛菌素、硫丹、高氰戊菊酯、乙虫腈、苯硫威、苯氧威、甲氰菊酯、氰戊菊酯、氟虫腈、氟啶虫酰胺、氟虫双酰胺、氟氰戊菊酯、τ-氟胺氰菊酯、嘧虫胺(UR-50701)、氟虫脲、地虫硫磷、氯虫酰肼、氟铃脲、氟蚁腙、吡虫啉、茚虫威、异柳磷、虱螨脲、马拉硫磷、氰氟虫腙、四聚乙醛、甲胺磷、杀扑磷、灭多虫、烯虫酯、甲氧氯、甲氧苄氟菊酯、久效磷、甲氧虫酰肼、烯啶虫胺、硝乙脲噻唑、双苯氟脲、多氟脲(XDE-007)、杀线威、对硫磷、甲基对硫磷、苄氯菊酯、甲拌磷、伏杀磷、亚胺硫磷、磷胺、抗蚜威、丙溴磷、丙氟菊酯、吡蚜酮、啶吡唑虫胺、除虫菊酯、啶虫丙醚、氟虫吡喹、吡唑虫啶、蚊蝇醚、鱼藤酮、利阿诺定、乙基多杀菌素、多杀菌素、螺螨酯、螺甲螨酯(BSN 2060)、螺虫乙酯、硫丙磷、虫酰肼、氟苯脲、七氟菊酯、特丁硫磷、杀虫威、噻虫啉、噻虫嗪、硫双威、杀虫双、四溴菊酯、唑蚜威、敌百虫和杀虫隆;或者
杀细菌剂,所述杀细菌剂选自链霉素;或者
杀螨剂,所述杀螨剂选自双甲脒、灭螨猛、乙酯杀螨醇、腈吡螨酯、三环锡、三氯杀螨醇、除螨灵、乙螨唑、喹螨醚、苯丁锡、甲氰菊酯、唑螨酯、噻螨酮、克螨特、哒螨灵和吡螨胺;或者
生物试剂,所述生物试剂选自苏云金芽孢杆菌、苏云金芽孢杆菌δ内毒素、杆状病毒、和昆虫病原细菌、病毒以及真菌。
13.根据权利要求1至12中任一项所述的杀真菌组合物,其中,所述组合物进一步包含农业上可接受的载体,以及任选地表面活性剂和/或配制辅助剂。
14.一种控制或预防有用植物或其繁殖材料上的植物病原性病害、尤其是植物病原性真菌的方法,所述方法包括将如权利要求1至12中任一项所定义的杀真菌组合物施用到所述有用植物、其场所或其繁殖材料上。
15.根据权利要求14所述的方法,其中将所述组合物组分(A)和(B)以顺序的方式进行施用。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB2003214.0A GB202003214D0 (en) | 2020-03-05 | 2020-03-05 | Fungicidal compositions |
GB2003214.0 | 2020-03-05 | ||
GB2020137.2 | 2020-12-18 | ||
GBGB2020137.2A GB202020137D0 (en) | 2020-12-18 | 2020-12-18 | Fungicidal compositions |
PCT/EP2021/055593 WO2021176057A1 (en) | 2020-03-05 | 2021-03-05 | Fungicidal compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
CN115209735A true CN115209735A (zh) | 2022-10-18 |
Family
ID=74870799
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202180018462.4A Pending CN115209735A (zh) | 2020-03-05 | 2021-03-05 | 杀真菌组合物 |
Country Status (11)
Country | Link |
---|---|
US (1) | US20230125322A1 (zh) |
EP (1) | EP4114183A1 (zh) |
JP (1) | JP2023517303A (zh) |
KR (1) | KR20220150909A (zh) |
CN (1) | CN115209735A (zh) |
AU (1) | AU2021231316A1 (zh) |
BR (1) | BR112022016993A2 (zh) |
CA (1) | CA3169015A1 (zh) |
CO (1) | CO2022012183A2 (zh) |
UY (1) | UY39115A (zh) |
WO (1) | WO2021176057A1 (zh) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB202214203D0 (en) | 2022-09-28 | 2022-11-09 | Syngenta Crop Protection Ag | Fungicidal compositions |
GB202214202D0 (en) | 2022-09-28 | 2022-11-09 | Syngenta Crop Protection Ag | Agricultural methods |
KR102600888B1 (ko) * | 2023-04-11 | 2023-11-13 | 주식회사 엘에프에프 | 유기태화 요오드 또는 유기태화 요오드 및 황을 유효성분으로 함유하고 과수 화상병을 포함하는 식물 병원성 세균 방제용 조성물 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0212859A2 (en) * | 1985-08-22 | 1987-03-04 | Imperial Chemical Industries Plc | Fungicides |
WO2001000562A1 (fr) * | 1999-06-25 | 2001-01-04 | Sumitomo Chemical Company, Limited | Derives d'acide acrylique, leur utilisation et intermediaires pour leur preparation |
CN102458111A (zh) * | 2009-06-25 | 2012-05-16 | 巴斯夫欧洲公司 | 农化混合物在提高植物健康中的用途 |
WO2020027214A1 (ja) * | 2018-07-31 | 2020-02-06 | 住友化学株式会社 | Qo阻害剤に対して耐性を有するダイズさび病菌の防除方法 |
WO2020193387A1 (en) * | 2019-03-22 | 2020-10-01 | Syngenta Crop Protection Ag | Fungicidal compounds |
Family Cites Families (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2751642B1 (fr) | 1996-07-24 | 1998-09-11 | Hoechst Schering Agrevo Sa | Nouveaux derives de l'acide beta-methoxy acrylique, leur procede de preparation et leur application comme pesticides |
ES2388548T3 (es) | 2005-04-08 | 2012-10-16 | Bayer Cropscience Nv | Suceso de élite A2704-12 y métodos y estuches para identificar a dicho suceso en muestras biológicas |
CA2603949C (en) | 2005-04-11 | 2014-12-09 | Bayer Bioscience N.V. | Elite event a5547-127 and methods and kits for identifying such event in biological samples |
AP2693A (en) | 2005-05-27 | 2013-07-16 | Monsanto Technology Llc | Soybean event MON89788 and methods for detection thereof |
US7951995B2 (en) | 2006-06-28 | 2011-05-31 | Pioneer Hi-Bred International, Inc. | Soybean event 3560.4.3.5 and compositions and methods for the identification and detection thereof |
CA2666754C (en) | 2006-10-31 | 2016-11-29 | E. I. Du Pont De Nemours And Company | Soybean event dp-305423-1 and compositions and methods for the identification and/or detection thereof |
BR122017018105B1 (pt) | 2007-11-15 | 2024-01-23 | Monsanto Technology Llc | Molécula de dna genômico de soja transgênica |
CA2748973A1 (en) | 2009-01-07 | 2010-07-15 | Basf Agrochemical Products B.V. | Soybean event 127 and methods related thereto |
AU2010284285B2 (en) | 2009-08-19 | 2015-08-20 | Dow Agrosciences Llc | Control of AAD-1 monocot volunteers in fields of dicot crops |
WO2011022469A2 (en) | 2009-08-19 | 2011-02-24 | Dow Agrosciences Llc | Aad-1 event das-40278-9, related transgenic corn lines, and event-specific identification thereof |
KR101772638B1 (ko) | 2009-08-19 | 2017-08-31 | 다우 아그로사이언시즈 엘엘씨 | Aad-1 이벤트 das-40278-9의 검출 |
EP3127425B1 (en) | 2009-09-17 | 2021-02-17 | Monsanto Technology LLC | Soybean transgenic event mon 87708 and methods of use thereof |
CN103270041A (zh) | 2010-05-06 | 2013-08-28 | 拜尔农作物科学股份公司 | 二噻英-四羧基-二酰亚胺的制备方法 |
TWI667347B (zh) | 2010-12-15 | 2019-08-01 | 瑞士商先正達合夥公司 | 大豆品種syht0h2及偵測其之組合物及方法 |
BR102012019436B8 (pt) | 2011-07-26 | 2022-10-11 | Dow Agrosciences Llc | Método de detecção do evento de soja pdab9582.814.19.1 |
MA37825B1 (fr) | 2012-07-04 | 2016-06-30 | Agro Kanesho Co Ltd | Dérivé d'ester d'acide 2-aminonicotinique et bactéricide le contenant comme principe actif |
EA027009B1 (ru) | 2012-12-19 | 2017-06-30 | Байер Кропсайенс Акциенгезельшафт | Дифторметилникотиновые инданилкарбоксамиды |
US20160029631A1 (en) | 2013-04-19 | 2016-02-04 | Bayer Cropscience Aktiengesellschaft | Method for combating pests |
CR20200207A (es) | 2013-06-14 | 2020-07-19 | Monsanto Technology Llc | EVENTO TRANSGÈNICO DE SOJA MON87751 Y MÈTODOS PARA SU DETECCIÒN Y USO (Divisional 2016-0020) |
US10173983B2 (en) | 2014-04-11 | 2019-01-08 | Syngenta Participations Ag | Fungicidal pyridylamidines |
CN111892576A (zh) | 2015-03-27 | 2020-11-06 | 先正达参股股份有限公司 | 杀微生物的杂二环衍生物 |
WO2016156290A1 (en) | 2015-04-02 | 2016-10-06 | Bayer Cropscience Aktiengesellschaft | Novel 5-substituted imidazole derivatives |
JP2018522846A (ja) | 2015-06-15 | 2018-08-16 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | ハロゲン置換フェノキシフェニルアミジン類及び殺菌剤としてのそれらの使用 |
AU2016305250B2 (en) | 2015-08-12 | 2020-10-22 | Syngenta Participations Ag | Microbiocidal heterobicyclic derivatives |
KR20180037267A (ko) | 2015-08-14 | 2018-04-11 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 트리아졸 유도체, 그의 중간체 및 살진균제로서의 그의 용도 |
JP6864673B2 (ja) | 2015-10-02 | 2021-04-28 | シンジェンタ パーティシペーションズ アーゲー | 殺微生物オキサジアゾール誘導体 |
WO2017055473A1 (en) | 2015-10-02 | 2017-04-06 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
US10640497B2 (en) | 2015-12-02 | 2020-05-05 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
UY37062A (es) | 2016-01-08 | 2017-08-31 | Syngenta Participations Ag | Derivados de aryl oxadiazol fungicidas |
CR20180434A (es) | 2016-03-10 | 2018-11-21 | Syngenta Participations Ag | Derivados microbiocidas de tipo (tio) carboxamida de la quinolina |
AR108745A1 (es) | 2016-06-21 | 2018-09-19 | Syngenta Participations Ag | Derivados de oxadiazol microbiocidas |
US10653146B2 (en) | 2016-10-06 | 2020-05-19 | Syngenta Participations Ag | Microbiocidal oxadiazole derivatives |
WO2018153707A1 (en) | 2017-02-22 | 2018-08-30 | Basf Se | Crystalline forms of a strobilurin type compound for combating phytopathogenic fungi |
UY37623A (es) | 2017-03-03 | 2018-09-28 | Syngenta Participations Ag | Derivados de oxadiazol tiofeno fungicidas |
US20210084902A1 (en) | 2017-05-02 | 2021-03-25 | Basf Se | Fungicidal mixture comprising substituted 3-phenyl-5-(trifluoromethyl)-1,2,4-oxadiazoles |
US11154058B2 (en) | 2017-06-14 | 2021-10-26 | Syngenta Participations Ag | Fungicidal compositions |
EP3720846A1 (en) | 2017-12-04 | 2020-10-14 | Syngenta Participations AG | Microbiocidal phenylamidine derivatives |
JP2020079269A (ja) * | 2020-01-31 | 2020-05-28 | 住友化学株式会社 | 植物病害防除方法 |
JP2021035986A (ja) * | 2020-11-16 | 2021-03-04 | 住友化学株式会社 | 有害生物防除方法 |
-
2021
- 2021-03-04 UY UY0001039115A patent/UY39115A/es unknown
- 2021-03-05 WO PCT/EP2021/055593 patent/WO2021176057A1/en unknown
- 2021-03-05 EP EP21711191.3A patent/EP4114183A1/en active Pending
- 2021-03-05 BR BR112022016993A patent/BR112022016993A2/pt unknown
- 2021-03-05 KR KR1020227031612A patent/KR20220150909A/ko active Search and Examination
- 2021-03-05 US US17/905,472 patent/US20230125322A1/en active Pending
- 2021-03-05 AU AU2021231316A patent/AU2021231316A1/en active Pending
- 2021-03-05 JP JP2022552960A patent/JP2023517303A/ja active Pending
- 2021-03-05 CA CA3169015A patent/CA3169015A1/en active Pending
- 2021-03-05 CN CN202180018462.4A patent/CN115209735A/zh active Pending
-
2022
- 2022-08-26 CO CONC2022/0012183A patent/CO2022012183A2/es unknown
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0212859A2 (en) * | 1985-08-22 | 1987-03-04 | Imperial Chemical Industries Plc | Fungicides |
US4802913A (en) * | 1985-08-22 | 1989-02-07 | Imperial Chemical Industries Plc | Fungicidal alpha-substituted acrylates |
WO2001000562A1 (fr) * | 1999-06-25 | 2001-01-04 | Sumitomo Chemical Company, Limited | Derives d'acide acrylique, leur utilisation et intermediaires pour leur preparation |
CN102458111A (zh) * | 2009-06-25 | 2012-05-16 | 巴斯夫欧洲公司 | 农化混合物在提高植物健康中的用途 |
WO2020027214A1 (ja) * | 2018-07-31 | 2020-02-06 | 住友化学株式会社 | Qo阻害剤に対して耐性を有するダイズさび病菌の防除方法 |
WO2020193387A1 (en) * | 2019-03-22 | 2020-10-01 | Syngenta Crop Protection Ag | Fungicidal compounds |
Also Published As
Publication number | Publication date |
---|---|
BR112022016993A2 (pt) | 2022-10-25 |
CA3169015A1 (en) | 2021-09-10 |
EP4114183A1 (en) | 2023-01-11 |
WO2021176057A1 (en) | 2021-09-10 |
US20230125322A1 (en) | 2023-04-27 |
AU2021231316A1 (en) | 2022-09-22 |
UY39115A (es) | 2021-10-29 |
JP2023517303A (ja) | 2023-04-25 |
KR20220150909A (ko) | 2022-11-11 |
CO2022012183A2 (es) | 2022-08-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN108135170B (zh) | 杀真菌组合物 | |
CN113646295A (zh) | 杀真菌化合物 | |
CN113382988A (zh) | 杀微生物2-酰基氨基-噻唑-4-甲酰胺衍生物 | |
CN113966171A (zh) | 杀真菌组合物 | |
CN115209735A (zh) | 杀真菌组合物 | |
CN113166082A (zh) | 杀微生物的噻唑衍生物 | |
CN113646304A (zh) | 杀微生物的噻唑衍生物 | |
CN115697063A (zh) | 杀真菌组合物 | |
JP2024512693A (ja) | 殺微生物性キノリン/キノキサリンベンゾチアジン誘導体 | |
CN114072384A (zh) | 杀微生物的吡啶酰胺衍生物 | |
CN115209736A (zh) | 杀真菌组合物 | |
CN115802893A (zh) | 杀真菌组合物 | |
EA046368B1 (ru) | Фунгицидные композиции | |
OA20877A (en) | Fungicidal compositions. | |
EA046405B1 (ru) | Фунгицидные композиции | |
OA20876A (en) | Fungicidal compositions | |
TW202339621A (zh) | 殺真菌組成物 | |
CN117241668A (zh) | 杀微生物的喹啉/喹喔啉苯并噻嗪衍生物 | |
CN117177963A (zh) | 杀微生物的喹啉/喹喔啉异喹啉衍生物 | |
CN115190761A (zh) | 控制或预防植物被植物病原性微生物多主棒孢菌侵染的方法 | |
JP2023516795A (ja) | 植物病原性微生物コリネスポラ・カッシイコラ(Corynespora cassiicola)による植物の被害を防除又は防止する方法 | |
JP2023516794A (ja) | 植物病原性微生物コリネスポラ・カッシイコラ(Corynespora cassiicola)による植物の被害を防除又は防止する方法 | |
JP2023550264A (ja) | 植物成長調節化合物 | |
CN116157015A (zh) | 植物生长调节剂化合物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination |