RU2012124764A - Комбинации активных соединений - Google Patents
Комбинации активных соединений Download PDFInfo
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- RU2012124764A RU2012124764A RU2012124764/13A RU2012124764A RU2012124764A RU 2012124764 A RU2012124764 A RU 2012124764A RU 2012124764/13 A RU2012124764/13 A RU 2012124764/13A RU 2012124764 A RU2012124764 A RU 2012124764A RU 2012124764 A RU2012124764 A RU 2012124764A
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- Prior art keywords
- methyl
- inhibitors
- furan
- amino
- active compounds
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims abstract 14
- 239000003112 inhibitor Substances 0.000 claims abstract 20
- 230000002438 mitochondrial effect Effects 0.000 claims abstract 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract 6
- 239000000018 receptor agonist Substances 0.000 claims abstract 6
- 229940044601 receptor agonist Drugs 0.000 claims abstract 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract 5
- 102000012440 Acetylcholinesterase Human genes 0.000 claims abstract 4
- 108010022752 Acetylcholinesterase Proteins 0.000 claims abstract 4
- 229920002101 Chitin Polymers 0.000 claims abstract 4
- 108010009685 Cholinergic Receptors Proteins 0.000 claims abstract 4
- 102000034337 acetylcholine receptors Human genes 0.000 claims abstract 4
- 229940022698 acetylcholinesterase Drugs 0.000 claims abstract 4
- 230000015572 biosynthetic process Effects 0.000 claims abstract 4
- 108010052164 Sodium Channels Proteins 0.000 claims abstract 3
- 102000018674 Sodium Channels Human genes 0.000 claims abstract 3
- 239000000664 voltage gated sodium channel blocking agent Substances 0.000 claims abstract 3
- 102000015782 Electron Transport Complex III Human genes 0.000 claims abstract 2
- 108010024882 Electron Transport Complex III Proteins 0.000 claims abstract 2
- 241000238631 Hexapoda Species 0.000 claims abstract 2
- 102000013379 Mitochondrial Proton-Translocating ATPases Human genes 0.000 claims abstract 2
- 108010026155 Mitochondrial Proton-Translocating ATPases Proteins 0.000 claims abstract 2
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 claims abstract 2
- 229940121373 acetyl-coa carboxylase inhibitor Drugs 0.000 claims abstract 2
- 239000000556 agonist Substances 0.000 claims abstract 2
- 230000003281 allosteric effect Effects 0.000 claims abstract 2
- 239000003467 chloride channel stimulating agent Substances 0.000 claims abstract 2
- 108010057988 ecdysone receptor Proteins 0.000 claims abstract 2
- 229960003692 gamma aminobutyric acid Drugs 0.000 claims abstract 2
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000003966 growth inhibitor Substances 0.000 claims abstract 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract 2
- 229930014550 juvenile hormone Natural products 0.000 claims abstract 2
- 239000002949 juvenile hormone Substances 0.000 claims abstract 2
- 150000003633 juvenile hormone derivatives Chemical class 0.000 claims abstract 2
- 239000012528 membrane Substances 0.000 claims abstract 2
- 230000000813 microbial effect Effects 0.000 claims abstract 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract 2
- 108010003516 norsynephrine receptor Proteins 0.000 claims abstract 2
- 230000010627 oxidative phosphorylation Effects 0.000 claims abstract 2
- 230000001105 regulatory effect Effects 0.000 claims abstract 2
- 150000003839 salts Chemical class 0.000 claims abstract 2
- 241000196324 Embryophyta Species 0.000 claims 8
- -1 butoxycarboxy Chemical group 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- ZCVAOQKBXKSDMS-PVAVHDDUSA-N (+)-trans-(S)-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-PVAVHDDUSA-N 0.000 claims 3
- 241000193388 Bacillus thuringiensis Species 0.000 claims 3
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims 3
- 229940097012 bacillus thuringiensis Drugs 0.000 claims 3
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products 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 claims 3
- 238000000034 method Methods 0.000 claims 3
- 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 claims 2
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- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims 2
- 241000607479 Yersinia pestis Species 0.000 claims 2
- 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 claims 2
- CJJOSEISRRTUQB-UHFFFAOYSA-N azinphos-methyl Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)N=NC2=C1 CJJOSEISRRTUQB-UHFFFAOYSA-N 0.000 claims 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 claims 2
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 claims 2
- 235000013399 edible fruits Nutrition 0.000 claims 2
- 230000003032 phytopathogenic effect Effects 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 239000002689 soil Substances 0.000 claims 2
- 230000009261 transgenic effect Effects 0.000 claims 2
- 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 claims 1
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 claims 1
- CXBMCYHAMVGWJQ-LOACHALJSA-N (1R)-tetramethrin Chemical compound CC1(C)C(C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-LOACHALJSA-N 0.000 claims 1
- KAATUXNTWXVJKI-GGPKGHCWSA-N (1R)-trans-(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-GGPKGHCWSA-N 0.000 claims 1
- XUNYDVLIZWUPAW-UHFFFAOYSA-N (4-chlorophenyl) n-(4-methylphenyl)sulfonylcarbamate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)OC1=CC=C(Cl)C=C1 XUNYDVLIZWUPAW-UHFFFAOYSA-N 0.000 claims 1
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 claims 1
- CFRPSFYHXJZSBI-DHZHZOJOSA-N (E)-nitenpyram Chemical compound [O-][N+](=O)/C=C(\NC)N(CC)CC1=CC=C(Cl)N=C1 CFRPSFYHXJZSBI-DHZHZOJOSA-N 0.000 claims 1
- FZRBKIRIBLNOAM-UHFFFAOYSA-N (E,E)-2-propynyl 3,7,11-trimethyl-2,4-dodecadienoate Chemical compound CC(C)CCCC(C)CC=CC(C)=CC(=O)OCC#C FZRBKIRIBLNOAM-UHFFFAOYSA-N 0.000 claims 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 claims 1
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 claims 1
- IAKOZHOLGAGEJT-UHFFFAOYSA-N 1,1,1-trichloro-2,2-bis(p-methoxyphenyl)-Ethane Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1 IAKOZHOLGAGEJT-UHFFFAOYSA-N 0.000 claims 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 claims 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 claims 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 1
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 claims 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 claims 1
- CMURKFSRGAWINZ-UHFFFAOYSA-N 2-(4-chloro-2,6-dimethylphenyl)-1-hydroxy-9,12-dioxa-4-azadispiro[4.2.4^{8}.2^{5}]tetradec-1-en-3-one Chemical compound CC1=CC(Cl)=CC(C)=C1C(C(N1)=O)=C(O)C11CCC2(OCCO2)CC1 CMURKFSRGAWINZ-UHFFFAOYSA-N 0.000 claims 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 claims 1
- VVRPVKDXGLLBDP-UHFFFAOYSA-N 2-chloro-5-(methoxymethyl)pyridine Chemical compound COCC1=CC=C(Cl)N=C1 VVRPVKDXGLLBDP-UHFFFAOYSA-N 0.000 claims 1
- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims 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 claims 1
- CJXVXIQIPJXTIC-UHFFFAOYSA-N 3-[(2-chloro-1,3-thiazol-5-yl)methyl-(2-fluoroethyl)amino]-2h-furan-5-one Chemical compound C=1C(=O)OCC=1N(CCF)CC1=CN=C(Cl)S1 CJXVXIQIPJXTIC-UHFFFAOYSA-N 0.000 claims 1
- BOPIGKPPEFBBEB-UHFFFAOYSA-N 3-[(6-bromopyridin-3-yl)methyl-(2-fluoroethyl)amino]-2h-furan-5-one Chemical compound C=1C(=O)OCC=1N(CCF)CC1=CC=C(Br)N=C1 BOPIGKPPEFBBEB-UHFFFAOYSA-N 0.000 claims 1
- OWMFJKUIQNFOGY-UHFFFAOYSA-N 3-[(6-chloro-5-fluoropyridin-3-yl)methyl-cyclopropylamino]-2h-furan-5-one Chemical compound N1=C(Cl)C(F)=CC(CN(C2CC2)C=2COC(=O)C=2)=C1 OWMFJKUIQNFOGY-UHFFFAOYSA-N 0.000 claims 1
- QRURGXUYUFRZJU-UHFFFAOYSA-N 3-[(6-chloro-5-fluoropyridin-3-yl)methyl-methylamino]-2h-furan-5-one Chemical compound C=1C(=O)OCC=1N(C)CC1=CN=C(Cl)C(F)=C1 QRURGXUYUFRZJU-UHFFFAOYSA-N 0.000 claims 1
- SNNQRPYPSAJQKV-UHFFFAOYSA-N 3-[(6-chloropyridin-3-yl)methyl-(2-fluoroethyl)amino]-2h-furan-5-one Chemical compound C=1C(=O)OCC=1N(CCF)CC1=CC=C(Cl)N=C1 SNNQRPYPSAJQKV-UHFFFAOYSA-N 0.000 claims 1
- RQRMKMRFKZIYOG-UHFFFAOYSA-N 3-[(6-chloropyridin-3-yl)methyl-methylamino]-2h-furan-5-one Chemical compound C=1C(=O)OCC=1N(C)CC1=CC=C(Cl)N=C1 RQRMKMRFKZIYOG-UHFFFAOYSA-N 0.000 claims 1
- JPHQHJFHSAVFQJ-UHFFFAOYSA-N 3-[2,2-difluoroethyl-[(6-fluoropyridin-3-yl)methyl]amino]-2h-furan-5-one Chemical compound C=1C(=O)OCC=1N(CC(F)F)CC1=CC=C(F)N=C1 JPHQHJFHSAVFQJ-UHFFFAOYSA-N 0.000 claims 1
- UKPDFCZYKKAJTK-UHFFFAOYSA-N 3-[3-(4-fluorophenyl)-2,6-dimethylphenyl]-4-hydroxy-8-oxa-1-azaspiro[4.5]dec-3-en-2-one Chemical compound CC1=CC=C(C=2C=CC(F)=CC=2)C(C)=C1C(C(N1)=O)=C(O)C21CCOCC2 UKPDFCZYKKAJTK-UHFFFAOYSA-N 0.000 claims 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 claims 1
- PGYDGBCATBINCB-UHFFFAOYSA-N 4-diethoxyphosphoryl-n,n-dimethylaniline Chemical compound CCOP(=O)(OCC)C1=CC=C(N(C)C)C=C1 PGYDGBCATBINCB-UHFFFAOYSA-N 0.000 claims 1
- 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 claims 1
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 claims 1
- XJFIKRXIJXAJGH-UHFFFAOYSA-N 5-chloro-1,3-dihydroimidazo[4,5-b]pyridin-2-one Chemical group ClC1=CC=C2NC(=O)NC2=N1 XJFIKRXIJXAJGH-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- 239000005660 Abamectin Substances 0.000 claims 1
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- 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 claims 1
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- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims 1
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- GBAWQJNHVWMTLU-RQJHMYQMSA-N [(1R,5S)-7-chloro-6-bicyclo[3.2.0]hepta-2,6-dienyl] dimethyl phosphate Chemical compound C1=CC[C@@H]2C(OP(=O)(OC)OC)=C(Cl)[C@@H]21 GBAWQJNHVWMTLU-RQJHMYQMSA-N 0.000 claims 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 claims 1
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- HOKBIQDJCNTWST-UHFFFAOYSA-N phosphanylidenezinc;zinc Chemical compound [Zn].[Zn]=P.[Zn]=P HOKBIQDJCNTWST-UHFFFAOYSA-N 0.000 claims 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims 1
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- FITIWKDOCAUBQD-UHFFFAOYSA-N prothiofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(Cl)C=C1Cl FITIWKDOCAUBQD-UHFFFAOYSA-N 0.000 claims 1
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- 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 claims 1
- 229940015367 pyrethrum Drugs 0.000 claims 1
- CXJSOEPQXUCJSA-UHFFFAOYSA-N pyridaphenthion Chemical compound N1=C(OP(=S)(OCC)OCC)C=CC(=O)N1C1=CC=CC=C1 CXJSOEPQXUCJSA-UHFFFAOYSA-N 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- MIOBBYRMXGNORL-UHFFFAOYSA-N pyrifluquinazon Chemical compound C1C2=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C2N(C(=O)C)C(=O)N1NCC1=CC=CN=C1 MIOBBYRMXGNORL-UHFFFAOYSA-N 0.000 claims 1
- JYQUHIFYBATCCY-UHFFFAOYSA-N quinalphos Chemical compound C1=CC=CC2=NC(OP(=S)(OCC)OCC)=CN=C21 JYQUHIFYBATCCY-UHFFFAOYSA-N 0.000 claims 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 claims 1
- RDYMFSUJUZBWLH-AZVNHNRSSA-N qy5y9r7g0e Chemical compound C([C@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-AZVNHNRSSA-N 0.000 claims 1
- 229940080817 rotenone Drugs 0.000 claims 1
- 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 claims 1
- 102000042094 ryanodine receptor (TC 1.A.3.1) family Human genes 0.000 claims 1
- 108091052345 ryanodine receptor (TC 1.A.3.1) family Proteins 0.000 claims 1
- MSHXTAQSSIEBQS-UHFFFAOYSA-N s-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate;hydron;chloride Chemical compound [Cl-].NC(=O)SCC([NH+](C)C)CSC(N)=O MSHXTAQSSIEBQS-UHFFFAOYSA-N 0.000 claims 1
- HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 claims 1
- 239000004328 sodium tetraborate Substances 0.000 claims 1
- 235000010339 sodium tetraborate Nutrition 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 229940014213 spinosad Drugs 0.000 claims 1
- 125000003003 spiro group Chemical group 0.000 claims 1
- 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 1
- 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 1
- 239000004575 stone Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 1
- OBTWBSRJZRCYQV-UHFFFAOYSA-N sulfuryl difluoride Chemical compound FS(F)(=O)=O OBTWBSRJZRCYQV-UHFFFAOYSA-N 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 239000005936 tau-Fluvalinate Substances 0.000 claims 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 claims 1
- 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 1
- AWYOMXWDGWUJHS-UHFFFAOYSA-N tebupirimfos Chemical compound CCOP(=S)(OC(C)C)OC1=CN=C(C(C)(C)C)N=C1 AWYOMXWDGWUJHS-UHFFFAOYSA-N 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
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 claims 1
- MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 claims 1
- OPASCBHCTNRLRM-UHFFFAOYSA-N thiometon Chemical compound CCSCCSP(=S)(OC)OC OPASCBHCTNRLRM-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- WPALTCMYPARVNV-UHFFFAOYSA-N tolfenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(OC=3C=CC(C)=CC=3)=CC=2)=C1Cl WPALTCMYPARVNV-UHFFFAOYSA-N 0.000 claims 1
- DDVNRFNDOPPVQJ-HQJQHLMTSA-N transfluthrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=CC(F)=C1F DDVNRFNDOPPVQJ-HQJQHLMTSA-N 0.000 claims 1
- 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 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 claims 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 claims 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 claims 1
- 239000005943 zeta-Cypermethrin Substances 0.000 claims 1
- 229940048462 zinc phosphide Drugs 0.000 claims 1
- 108091006146 Channels Proteins 0.000 abstract 1
- 229940127437 Chloride Channel Antagonists Drugs 0.000 abstract 1
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 abstract 1
- 230000001419 dependent effect Effects 0.000 abstract 1
- 230000035764 nutrition Effects 0.000 abstract 1
- 235000016709 nutrition Nutrition 0.000 abstract 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/22—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom rings with more than six members
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
- A01N43/32—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms 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
-
- 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
- A01N43/72—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
- A01N43/74—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 one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Abstract
1. Комбинации активных соединений, содержащие(А) по меньшей мере один дитиинотетракарбоксимид формулы (I)в которой Rи Rидентичны и представляют собой метил, этил, н-пропил или изопропил, и n равно 0 или 1; или его агрохимически приемлемую соль,и(В) по меньшей мере одно другое активное соединение, выбранное из следующих групп(1) ингибиторы ацетилхолинэстеразы (АХЭ),(2) антагонисты ГАМК-регулируемых хлоридных каналов,(3) модуляторы натриевых каналов/блокаторы потенциалзависимых натриевых каналов,(4) агонисты никотинэргического ацетилхолинового рецептора,(5) аллостерические модуляторы ацетилхолинового рецептора (агонисты),(6) активаторы хлоридных каналов,(7) миметики ювенильного гормона,(8) смешанные неспецифические (мульти-сайтовые) ингибиторы,(9) селективные блокаторы питания равнокрылых,(10) ингибиторы роста клещей,(11) микробные разрушители мембран средней кишки насекомых,(12) ингибиторы митохондриальной АТФ-синтазы,(13) разобщители окислительного фосфорилирования посредством разрушения протонного градиента,(14) блокаторы канала никотинового ацетилхолинового рецептора,(15) ингибиторы биосинтеза хитина (тип 0),(16) ингибиторы биосинтеза хитина (тип 1),(17) ингибиторы линьки,(18) агонисты/деструкторы рецептора экдизона,(19) агонисты рецептора октопамина,(20) ингибиторы транспорта электронов митохондриального комплекса III,(21) ингибиторы транспорта электронов митохондриального комплекса I,(22) блокаторы потенциалзависимых натриевых каналов,(23) ингибиторы ацетил-КоА-карбоксилазы,(24) ингибиторы транспорта электронов митохондриального комплекса IV,(25) ингибиторы транспорта электронов митохондриального комплекса II,(26) модуляторы риан�
Claims (10)
1. Комбинации активных соединений, содержащие
(А) по меньшей мере один дитиинотетракарбоксимид формулы (I)
в которой R1 и R2 идентичны и представляют собой метил, этил, н-пропил или изопропил, и n равно 0 или 1; или его агрохимически приемлемую соль,
и
(В) по меньшей мере одно другое активное соединение, выбранное из следующих групп
(1) ингибиторы ацетилхолинэстеразы (АХЭ),
(2) антагонисты ГАМК-регулируемых хлоридных каналов,
(3) модуляторы натриевых каналов/блокаторы потенциалзависимых натриевых каналов,
(4) агонисты никотинэргического ацетилхолинового рецептора,
(5) аллостерические модуляторы ацетилхолинового рецептора (агонисты),
(6) активаторы хлоридных каналов,
(7) миметики ювенильного гормона,
(8) смешанные неспецифические (мульти-сайтовые) ингибиторы,
(9) селективные блокаторы питания равнокрылых,
(10) ингибиторы роста клещей,
(11) микробные разрушители мембран средней кишки насекомых,
(12) ингибиторы митохондриальной АТФ-синтазы,
(13) разобщители окислительного фосфорилирования посредством разрушения протонного градиента,
(14) блокаторы канала никотинового ацетилхолинового рецептора,
(15) ингибиторы биосинтеза хитина (тип 0),
(16) ингибиторы биосинтеза хитина (тип 1),
(17) ингибиторы линьки,
(18) агонисты/деструкторы рецептора экдизона,
(19) агонисты рецептора октопамина,
(20) ингибиторы транспорта электронов митохондриального комплекса III,
(21) ингибиторы транспорта электронов митохондриального комплекса I,
(22) блокаторы потенциалзависимых натриевых каналов,
(23) ингибиторы ацетил-КоА-карбоксилазы,
(24) ингибиторы транспорта электронов митохондриального комплекса IV,
(25) ингибиторы транспорта электронов митохондриального комплекса II,
(26) модуляторы рианодиновых рецепторов,
(27) другие инсектициды.
2. Комбинации активных соединений по п.1, в которых соединение формулы (I) представляет собой (I-1) 2,6-диметил-1Н,5Н-[1,4]дитиино [2,3-с:5,6-с']дипиррол-1,3,5,7(2Н,6Н)-тетрон.
3. Комбинации активных соединений по п.1 или 2, в которых другое активное соединение выбирается из группы, включающей (1А.1) аланикарб, (1А.2) алдикарб, (1А.3) бендиокарб, (1А.4) бенфуракарб, (1А.5) бутокарбоксим, (1А.6) бутоксикарбоксим, (1А.7) карбарил, (1А.8) карбофуран, (1А.9) карбосульфан, (1А.10) этиофенкарб, (1А.11) фенобукарб, (1А.12) форметанат, (1А.13) фуратиокарб, (1А.14) изопрокарб, (1А.15) метиокарб, (1А.16) метомил, (1А.17) метолкарб, (1А.18) оксамил, (1А.19) пиримикарб, (1А.20) пропоксур, (1А.21) тиодикарб, (1А.22) тиофанокс, (1А.23) триазамат, (1А.24) триметакарб, (1А.25) ХМС, (1А.26) ксилилкарб, (1В.1) ацефат, (1В.1) азаметифос, (1В.2) азинфос, (1В.3) азинфос-метил, (1В.4) азинфос-этил, (1В.5) кадусафос, (1В.6) хлорэтоксифос, (1В.7) хлорфенвинфос, (1В.8) хлорфенвинфос, (1В.9) хлормефос, (1В.10) хлорпирифос, (1В.11) хлорпирифос-метил, (1В.12), (1В.16) дихлорвос/DDVP, (1В.17) дикротофос, (1В.18) диметоат, (1В.19) диметилвинфос, (1В.20) дисульфотон, (1В.21) EPN, (1B.22) этион, (1В.23) этопрофос, (1В.24) фамфур, (1В.25) фенамифос, (1В.26) фенитротион, (1В.27) фентион, (1В.28) фостиазат, (1В.29) гептенофос, (1В.30) изофенфос, (1В.31) изопропил О-(метоксиаминотио-фосфорил) салицилат, (1В.32) изоксатион, (1В.33) малатион, (1В.34) мекарбам, (1В.35) метамидофос, (1В.36) метидатион, (1В.37) мевинфос, (1В.38) монокротофос, (1В. 39) налед, (1В.40) ометоат, (1В.41) оксидеметон-метил, (1В.42) паратион, (1В.43) паратион-метил, (1В.44) фентоат, (1В.45) форат, (1В.46) фосалон, (1В.47) фосмет, (1В.48) фосфамидон, (1В.49) фоксим, (1В.50) пиримифос, (1В.51) пиримифос-метил, (1В.52) профенофос, (1В.53) пропетамфос, (1В.54) протиофос, (1В.55) пираклофос, (1В.56) пиридафентион, (1В.57) хиналфос, (1В.58) сульфотеп, (1В.59) тебупиримфос, (1В.60) темефос, (1В.61) тербуфос, (1В.62) тетрахлорвинфос, (1В.63) тиометон, (1В.64) триазофос, (1В.65) триклорфон, (1В.66) вамидотион, (2А.1) хлордан (2А.2) эндосульфан (2А.3) альфа-эндосульфан, (2В.1) этипрол (2В.2) фипронил, (2В.3) пирафлупрол, (2В.4) пирипрол, (3А.1) акринатрин, (3А.2) аллетрин (3А.3), d-цис-транс-аллетрин, (3А.4) d-транс-аллетрин, (3А.5) бифентрин, (3А.6) биоаллетрин, (3А.7) биоаллетрин S-циклопентенил, (3А.8) биоресметрин, (3А.9) циклопротрин, (3А.10) цифлутрин, (3А.11) β-цифлутрин, (3А.12) цигалотрин, (3А.13) γ-цигалотрин, (3А.14) λ-цигалотрин, (3А.15) циперметрин, (3А.16) α-циперметрин, (3А.17) β-циперметрин, (3А.18) θ-циперметрин, (3А.19) ζ-циперметрин, (3А.20) цифенотрин [(1R)-транс-изомеры], (3А.21) дельтаметрин, (3А.22) димефлутрин, (3А.23) эмпетрин [(EZ) - (1R)-изомеры)], (3А.24) эсфенвалерат, (3А.25) этофенпрокс, (3А.26) фенпропатрин, (3А.27) фенвалерат, (3А.28) флуцитринат, (3А.29) флуметрин, (3А.30) флувалинат, (3А.31) тауфлувалинат, (3А.32) халфенпрокс, (3А.33) имипротрин, (3А.34) метофлутрин, (3А.35) перметрин, (3А.36) фенотрин [(1R)-транс-изомер)], (3А.37) праллетрин, (3А.38) профлутрин, (3А.39) пиретрин (пиретрум), (3А.40) ресметрин, (3А.41) RU 15525, (3А.42) силафлуофен, (3А.43) тефлутрин, (3А.44) тетраметрин [(1R)-изомеры)], (3А.45) тралометрин, (3А.46) трансфлутрин, (3А.47) ZXI 8901, (3В.1) DDT, (3B.2) метоксихлор, (4А.1) ацетамиприд, (4А.2) клотианидин, (4А.3) динотефуран, (4А.4) имидаклоприд, (4А.5) нитенпирам, (4А.6) тиаклоприд, (4А.7) тиаметоксам, (4.В.1) никотин, (5.1) спинеторам, (5.2) спиносад, (6.1) абамектин, (6.2) эмамектин бензоат, (6.3) лепимектин, (6.4) милбемектин, (7.1) гидропрен, (7.2) кинопрен, (7.3) метопрен, (7.4) феноксикарб, (7.5) пирипроксифен, (8А.1) метилбромид, (8В.1) хлорпикрин, (8В.2) сульфурилфторид, (8В.3) бура, (8В.4) рвотный камень, (9.1) пиметрозин, (9.2) флоникамид, (10.1) клофентезин, (10.2) дифловидазин, (10.3) гекситиазокс, (10.4) этоксазол, (11.1) Bacillus thuringiensis подвид israelensis, (11.2) Bacillus sphaericus, (11.3) Bacillus thuringiensis подвид aizawai, (11.4) Bacillus thuringiensis подвид kurstaki, (11.5) Bacillus thuringiensis подвид tenebrionis, ВТ-белки сельскохозяйственных культур: (11.6) Cry1Ab, (11.7) Cry1Ac, (11.8) Cry1Fa, (11.9) Cry2Ab, (11.10) mCry3A, (11.11) Cry3Ab, (11.12) Cry3Bb, (11.13) Cry34/35Ab1, (12A.1) диафентиурон, (12В.1) азоциклотин, (12В.2) цигексатин, (12В.3) фенбутатин оксид, (12С.1) пропаргит, (12С.2) тетрадифон, (13.1) хлорфенапир, (13.2) DNOC, (14.1) бенсултап, (14.2) картап гидрохлорид, (14, 3) тиоциклам, (14.4) тиосултап натрий, (15.1) бистрифлурон, (15.2) хлорфлуазурон, (15.3) дифлубензурон, (15.4) флуциклоксурон, (15.5) флуфеноксурон, (15.6) гексафлумурон, (15.7) луфенурон, (15.8) новалурон, (15.9) новифлумурон, (15.10) пенфлурон, (15.11) тефлубензурон, (15.12) трифлумурон, (16.1) бупрофезин, (17.1) циромазин, (18.1) хромафенозид, (18.2) галофенозид, (18.3) метоксифенозид, (18.4) тебуфенозид, (19.1) амитраз, (20.1) гидраметилнон, (20.2) ацехиноцил, (20.3) флуакрипирим, (21.1) феназахин, (21.2) фенпироксимат, (21.3) пиримидифен, (21.4) пиридабен, (21.5) тебуфенпирад, (21.6) толфенпирад, (21.7) ротенон, (22.1) индоксакарб, (22.2) метафлумизон, (23А.1) спиродиклофен, (23А.2) спиромесифен, (23В.1) спиротетрамат, (24А.1) фосфид алюминия, (24А.2) фосфид кальция, (24А.3) фосфин, (24А.4) фосфид цинка, (24В.1) цианид, (25.1) циенопирафен, (26.1) хлорантранилипрол (ринаксипир), (26.2) циантранилипрол (циазипир), (26.3) флубендиамид, (27.1) азадирахтин, (27.2) амидофлумет, (27.3) бензоксимат, (27.4) бифеназат, (27.5) хинометионат, (27.6) криолит, (27.7) цифлуметофен, (27.8) дикофол, (27.9) флуфенерим, (27.10) пиридалил, (27.11) пирифлухиназон; (27.12) 4-{[(6-бромпиридин-3-ил)метил](2-фторэтил)амино}фуран-2(5Н)-он, (27.13) 4-{[(6-фторпиридин-3-ил)метил](2,2-дифторэтил)амино}фуран-2(5Н)-он, (27.14) 4-{[(2-хлор-1,3-тиазол-5-ил)метил](2-фторэтил)амино}фуран-2(5Н)-он, (27.15) 4-{[(6-хлорпиридин-3-ил)метил](2-фторэтил)амино}фуран-2(5Н)-он, (27.16) 4-{[(6-хлорпиридин-3-ил)метил](2,2-дифторэтил)амино}фуран-2(5Н)-он, (27.17) 4-{[(6-хлор-5-фторпиридин-3-ил)метил](метил)амино}фуран-2(5Н)-он, (27.18) 4-{[(5,6-дихлорпиридин-3-ил)метил](2-фторэтил)амино}фуран-2(5Н)-он, (27.19) 4-{[(6-хлор-5-фторпиридин-3-ил)метил](циклопропил)амино}фуран-2(5Н)-он, (27.20) 4-{[(6-хпорпиридин-3-ил)метил](циклопропил)амино}фуран-2(5Н)-он, (27.21) 4-{[(6-хлорпиридин-3-ил)метил](метил)амино}фуран-2(5Н)-он, (27.22) [(6-хлорпиридин-3-ил)метил](метил)оксидо-λ4-сульфанилиденцианамид, (27.23) [1-(6-хпорпиридин-3-ил)этил](метил)оксидо-λ4-сульфанилиденцианамид и его диастереомеры, (27.24) {[(1R)-1-(6-хлорпиридин-3-ил)этил](метил)оксидо-λ6-сульфанилдиден}цианамид и (27.25) {[(1S)-1-(6-хлорпиридин-3-ил)этил](метил)оксидо-λ6-сульфанилиден}цианамид, (27.26) [(6-трифторметилпиридин-3-ил)метил](метил)оксидо-λ4-сульфанилиденамид или (27.27) сульфоксафлор, (27.28) 11-(4-хлор-2,6-диметилфенил)-12-гидрокси-1,4-диокса-9-азадиспиро[4.2.4.2]тетрадец-11-ен-10-он, (28.29) 3-(4'-фтор-2,4-диметилбифенил-3-ил)-4-гидрокси-8-окса-1-азаспиро[4.5]дец-3-ен-2-он и (28.30) 1-{2,4-диметил-5-[(2,2,2-трифторэтил)сульфинил]фенил}-3-(трифторметил)-1Н-1,2,4-триазол.
4. Композиции, содержащие комбинации активных соединений по п.1 и дополнительно содержащие вспомогательные вещества, растворители, носители, поверхностно-активные вещества или наполнители.
5. Способ контроля фитопатогенных грибов и/или животных вредителей при защите сельскохозяйственных культур, отличающийся тем, что комбинации активных соединений по п.1 или композиции по п.2 или 4 наносятся на семена, растение, плоды растений или на почву, на которой произрастает растение или предполагается его выращивание.
6. Способ по п.5, отличающийся тем, что обрабатываются растение, плоды растений или почва, на которой растение произрастает или предполагается его выращивание.
7. Способ по п.5, отличающийся тем, что при обработке листьев применяется от 0,1 до 10000 г/га и при обработке семян применяется от 2 до 200 г на 100 кг семян.
8. Применение комбинаций активных соединений по п.1 или композиций по п.2 или 4 для контроля нежелательных фитопатогенных грибов и/или животных вредителей для защиты сельскохозяйственных культур.
9. Применение комбинаций активных соединений по п.1 или композиций по п.2 или 4 для обработки семян, семян трансгенных растений и трансгенных растений.
10. Семена, обработанные комбинациями активных соединений по п.1 или композициями по п.2 или 4.
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| BRPI0920122B1 (pt) * | 2008-10-15 | 2017-12-19 | Bayer Intellectual Property Gmbh | Ditiin-tetracarboximides and their uses for combating phytopathogenic fungi |
| AR077956A1 (es) * | 2009-09-14 | 2011-10-05 | Bayer Cropscience Ag | Combinaciones de compuestos activos |
| KR20130057994A (ko) * | 2010-04-14 | 2013-06-03 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 디티이노-테트라카복사미드 유도체 및 미생물 또는 이소플라본의 살진균성 배합물 |
| US20140296536A1 (en) * | 2011-10-13 | 2014-10-02 | Bayer Intellectual Prooperty GmbH | Method for producing dithiine tetracarboximides |
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- 2010-11-15 MX MX2012005638A patent/MX2012005638A/es active IP Right Grant
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- 2010-11-15 AR ARP100104217A patent/AR079609A1/es unknown
- 2010-11-15 PH PH1/2012/500972A patent/PH12012500972A1/en unknown
- 2010-11-15 KR KR1020127015631A patent/KR20120096511A/ko not_active Ceased
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- 2010-11-15 EP EP10781870A patent/EP2501235A1/en not_active Withdrawn
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Also Published As
| Publication number | Publication date |
|---|---|
| AR079609A1 (es) | 2012-02-08 |
| BR112012011663A2 (pt) | 2015-10-13 |
| UY33036A (es) | 2011-06-30 |
| CN103478148A (zh) | 2014-01-01 |
| CN102711478A (zh) | 2012-10-03 |
| EP2501235A1 (en) | 2012-09-26 |
| US8481456B2 (en) | 2013-07-09 |
| US20110118115A1 (en) | 2011-05-19 |
| KR20120096511A (ko) | 2012-08-30 |
| UA108216C2 (ru) | 2015-04-10 |
| CR20120251A (es) | 2012-09-14 |
| CN102711478B (zh) | 2014-09-17 |
| JP2013510895A (ja) | 2013-03-28 |
| RU2565081C2 (ru) | 2015-10-20 |
| US20130296167A1 (en) | 2013-11-07 |
| CN103478148B (zh) | 2015-04-22 |
| US8916500B2 (en) | 2014-12-23 |
| MX2012005638A (es) | 2012-06-13 |
| PH12012500972A1 (en) | 2013-01-07 |
| AU2010320995B2 (en) | 2015-01-15 |
| GT201200149A (es) | 2013-08-21 |
| JP5852579B2 (ja) | 2016-02-03 |
| ZA201203414B (en) | 2013-08-28 |
| ECSP12011901A (es) | 2012-07-31 |
| AU2010320995A1 (en) | 2012-06-07 |
| CA2780841A1 (en) | 2011-05-26 |
| CO6551680A2 (es) | 2012-10-31 |
| WO2011061156A1 (en) | 2011-05-26 |
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