ES2287905T3 - Composicion fungicida que comprende un derivado de piridiletilbenzamida y un compuesto capaz de inhibir la biosintesis de ergosterol. - Google Patents
Composicion fungicida que comprende un derivado de piridiletilbenzamida y un compuesto capaz de inhibir la biosintesis de ergosterol. Download PDFInfo
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- ES2287905T3 ES2287905T3 ES05715942T ES05715942T ES2287905T3 ES 2287905 T3 ES2287905 T3 ES 2287905T3 ES 05715942 T ES05715942 T ES 05715942T ES 05715942 T ES05715942 T ES 05715942T ES 2287905 T3 ES2287905 T3 ES 2287905T3
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- 239000000203 mixture Substances 0.000 title claims abstract description 124
- 230000008686 ergosterol biosynthesis Effects 0.000 title claims abstract description 14
- 230000002401 inhibitory effect Effects 0.000 title claims abstract description 14
- 230000000855 fungicidal effect Effects 0.000 title claims description 15
- 239000000417 fungicide Substances 0.000 title claims description 5
- 239000002131 composite material Substances 0.000 title 1
- -1 amino, phenoxy Chemical group 0.000 claims abstract description 37
- 150000001875 compounds Chemical class 0.000 claims abstract description 37
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 11
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 10
- 150000002367 halogens Chemical class 0.000 claims abstract description 10
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
- 125000001424 substituent group Chemical group 0.000 claims abstract description 6
- 150000002148 esters Chemical class 0.000 claims abstract description 5
- 125000000304 alkynyl group Chemical group 0.000 claims abstract description 4
- 125000002252 acyl group Chemical group 0.000 claims abstract description 3
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 3
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 3
- 125000005082 alkoxyalkenyl group Chemical group 0.000 claims abstract description 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 3
- 125000004422 alkyl sulphonamide group Chemical group 0.000 claims abstract description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract description 3
- 125000004103 aminoalkyl group Chemical group 0.000 claims abstract description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 3
- 125000004663 dialkyl amino group Chemical group 0.000 claims abstract description 3
- 125000004438 haloalkoxy group Chemical group 0.000 claims abstract description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims abstract description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 2
- 238000000034 method Methods 0.000 claims description 26
- 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 19
- 239000005837 Spiroxamine Substances 0.000 claims description 14
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 claims description 14
- 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 11
- 239000005839 Tebuconazole Substances 0.000 claims description 11
- 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 claims description 9
- 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 8
- 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 8
- 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 8
- 239000005767 Epoxiconazole Substances 0.000 claims description 8
- 239000005868 Metconazole Substances 0.000 claims description 8
- 239000005820 Prochloraz Substances 0.000 claims description 8
- 239000005822 Propiconazole Substances 0.000 claims description 8
- 239000005846 Triadimenol Substances 0.000 claims description 8
- 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 8
- 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 8
- 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 8
- 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 claims description 8
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical group ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 claims description 7
- 239000005785 Fluquinconazole Substances 0.000 claims description 7
- 235000013399 edible fruits Nutrition 0.000 claims description 7
- 229960002125 enilconazole Drugs 0.000 claims description 7
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 claims description 7
- 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 7
- 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 6
- 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 6
- 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 6
- 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 6
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 claims description 6
- 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 6
- 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 6
- 239000005741 Bromuconazole Substances 0.000 claims description 6
- 239000005775 Fenbuconazole Substances 0.000 claims description 6
- 239000005787 Flutriafol Substances 0.000 claims description 6
- 239000005795 Imazalil Substances 0.000 claims description 6
- 239000005796 Ipconazole Substances 0.000 claims description 6
- 239000005813 Penconazole Substances 0.000 claims description 6
- 239000005840 Tetraconazole Substances 0.000 claims description 6
- 239000005859 Triticonazole Substances 0.000 claims description 6
- AKNQMEBLVAMSNZ-UHFFFAOYSA-N azaconazole Chemical group ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCCO1 AKNQMEBLVAMSNZ-UHFFFAOYSA-N 0.000 claims description 6
- 229950000294 azaconazole Drugs 0.000 claims description 6
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 claims description 6
- 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 6
- 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 6
- 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 6
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 claims description 6
- 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 6
- 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 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 6
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical group C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 claims description 5
- 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 claims description 5
- ZOMKCDYJHAQMCU-UHFFFAOYSA-N 4-butyl-1,2,4-triazole Chemical group CCCCN1C=NN=C1 ZOMKCDYJHAQMCU-UHFFFAOYSA-N 0.000 claims description 5
- LXMQMMSGERCRSU-UHFFFAOYSA-N Fluotrimazole Chemical compound FC(F)(F)C1=CC=CC(C(C=2C=CC=CC=2)(C=2C=CC=CC=2)N2N=CN=C2)=C1 LXMQMMSGERCRSU-UHFFFAOYSA-N 0.000 claims description 5
- 241000233866 Fungi Species 0.000 claims description 5
- ULCWZQJLFZEXCS-KGLIPLIRSA-N Furconazole-cis Chemical compound O1[C@@H](OCC(F)(F)F)CC[C@@]1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 ULCWZQJLFZEXCS-KGLIPLIRSA-N 0.000 claims description 5
- BABJTMNVJXLAEX-UHFFFAOYSA-N Triamiphos Chemical compound N1=C(N)N(P(=O)(N(C)C)N(C)C)N=C1C1=CC=CC=C1 BABJTMNVJXLAEX-UHFFFAOYSA-N 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 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 5
- 150000002460 imidazoles Chemical class 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- 150000002780 morpholines Chemical class 0.000 claims description 5
- 150000003053 piperidines Chemical class 0.000 claims description 5
- 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 claims description 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- 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 claims description 3
- IKNXXTIMVROREQ-WXXKFALUSA-N (e)-but-2-enedioic acid;[2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl]-imidazol-1-ylmethanone Chemical compound OC(=O)\C=C\C(O)=O.C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1.C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 IKNXXTIMVROREQ-WXXKFALUSA-N 0.000 claims description 3
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 claims description 3
- 239000005730 Azoxystrobin Substances 0.000 claims description 3
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 claims description 3
- 239000005750 Copper hydroxide Substances 0.000 claims description 3
- 239000005752 Copper oxychloride Substances 0.000 claims description 3
- 239000005764 Dithianon Substances 0.000 claims description 3
- 239000005766 Dodine Substances 0.000 claims description 3
- 239000005784 Fluoxastrobin Substances 0.000 claims description 3
- 239000005802 Mancozeb Substances 0.000 claims description 3
- 239000005818 Picoxystrobin Substances 0.000 claims description 3
- 239000005823 Propineb Substances 0.000 claims description 3
- 239000005869 Pyraclostrobin Substances 0.000 claims description 3
- 239000005828 Pyrimethanil Substances 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 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 3
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 claims description 3
- 229910001956 copper hydroxide Inorganic materials 0.000 claims description 3
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims description 3
- VNZQQAVATKSIBR-UHFFFAOYSA-L copper;octanoate Chemical compound [Cu+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O VNZQQAVATKSIBR-UHFFFAOYSA-L 0.000 claims description 3
- 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 claims description 3
- 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 3
- 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 3
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 claims description 3
- 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 3
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000004308 thiabendazole Substances 0.000 claims description 3
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims description 3
- 235000010296 thiabendazole Nutrition 0.000 claims description 3
- 229960004546 thiabendazole Drugs 0.000 claims description 3
- 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 description 3
- URDNHJIVMYZFRT-KGLIPLIRSA-N (2r,3r)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pentan-3-ol Chemical compound C([C@H]([C@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1Cl URDNHJIVMYZFRT-KGLIPLIRSA-N 0.000 claims description 2
- ZQMRDENWZKMOTM-UHFFFAOYSA-N 2-butoxy-6-iodo-3-propylchromen-4-one Chemical compound C1=C(I)C=C2C(=O)C(CCC)=C(OCCCC)OC2=C1 ZQMRDENWZKMOTM-UHFFFAOYSA-N 0.000 claims description 2
- 239000005762 Dimoxystrobin Substances 0.000 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 2
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- 239000005857 Trifloxystrobin Substances 0.000 claims description 2
- 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 2
- 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 2
- 231100001184 nonphytotoxic Toxicity 0.000 claims description 2
- 230000003032 phytopathogenic effect Effects 0.000 claims description 2
- 239000002689 soil Substances 0.000 claims description 2
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 2
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 claims description 2
- 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 2
- MZWDAEVXPZRJTQ-WUXMJOGZSA-N 4-[(e)-(4-fluorophenyl)methylideneamino]-3-methyl-1h-1,2,4-triazole-5-thione Chemical compound CC1=NNC(=S)N1\N=C\C1=CC=C(F)C=C1 MZWDAEVXPZRJTQ-WUXMJOGZSA-N 0.000 claims 1
- 229910000365 copper sulfate Inorganic materials 0.000 claims 1
- 239000000945 filler Substances 0.000 claims 1
- 150000003852 triazoles Chemical class 0.000 claims 1
- 229940125904 compound 1 Drugs 0.000 description 83
- 241000196324 Embryophyta Species 0.000 description 76
- 229940125782 compound 2 Drugs 0.000 description 47
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- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 25
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- 235000021012 strawberries Nutrition 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000002641 tar oil Substances 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 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 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- 239000004560 ultra-low volume (ULV) liquid Substances 0.000 description 1
- 239000004555 ultra-low volume (ULV) suspension Substances 0.000 description 1
- 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 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000004552 water soluble powder Substances 0.000 description 1
- 239000004554 water soluble tablet Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent Substances 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
- 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
- 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
- A01N37/18—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 the group โCOโN<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—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 the group โCOโN<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- A01N37/24—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 the group โCOโN<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides containing at least one oxygen or sulfur atom being directly attached to the same aromatic ring system
-
- 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
- A01N43/26—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 five-membered rings
- A01N43/28—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 five-membered rings with two hetero atoms in positions 1,3
- A01N43/30—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 five-membered rings with two hetero atoms in positions 1,3 with two oxygen atoms in positions 1,3, condensed with a carbocyclic ring
-
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/60—1,4-Diazines; Hydrogenated 1,4-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
- A01N43/64—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
- A01N43/72—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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Pyridine Compounds (AREA)
- Saccharide Compounds (AREA)
- Carbon And Carbon Compounds (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04356014A EP1563731A1 (en) | 2004-02-12 | 2004-02-12 | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the ergosterol biosynthesis |
| EP04356014 | 2004-02-12 | ||
| US63695604P | 2004-12-17 | 2004-12-17 | |
| US636956P | 2004-12-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2287905T3 true ES2287905T3 (es) | 2007-12-16 |
Family
ID=34684798
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES05715942T Expired - Lifetime ES2287905T3 (es) | 2004-02-12 | 2005-02-10 | Composicion fungicida que comprende un derivado de piridiletilbenzamida y un compuesto capaz de inhibir la biosintesis de ergosterol. |
Country Status (30)
| Country | Link |
|---|---|
| US (5) | US8168660B2 (enExample) |
| EP (2) | EP1563731A1 (enExample) |
| JP (1) | JP4685035B2 (enExample) |
| KR (1) | KR100838541B1 (enExample) |
| CN (2) | CN101978828B (enExample) |
| AT (1) | ATE367088T1 (enExample) |
| AU (1) | AU2005213186B9 (enExample) |
| BE (3) | BE2014C014I2 (enExample) |
| BR (1) | BRPI0506617B1 (enExample) |
| CA (1) | CA2551149C (enExample) |
| CO (1) | CO5720996A2 (enExample) |
| CR (1) | CR8609A (enExample) |
| DE (1) | DE602005001701T2 (enExample) |
| DK (1) | DK1729576T3 (enExample) |
| EC (1) | ECSP066838A (enExample) |
| ES (1) | ES2287905T3 (enExample) |
| FR (2) | FR14C0046I2 (enExample) |
| HU (3) | HUS1400036I1 (enExample) |
| IL (1) | IL176834A (enExample) |
| LT (1) | LTC1729576I2 (enExample) |
| LU (2) | LU92503I2 (enExample) |
| MA (1) | MA28460B1 (enExample) |
| NL (2) | NL350068I1 (enExample) |
| NZ (1) | NZ548019A (enExample) |
| PT (1) | PT1729576E (enExample) |
| RU (1) | RU2362302C3 (enExample) |
| SI (1) | SI1729576T1 (enExample) |
| UA (1) | UA84056C2 (enExample) |
| WO (1) | WO2005077183A1 (enExample) |
| ZA (1) | ZA200606377B (enExample) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19962470A1 (de) * | 1999-12-22 | 2001-07-12 | Schulz Hans Herrmann | Verwendung von Chemotherapeutika |
| WO2005074684A2 (en) | 2004-02-04 | 2005-08-18 | Janssen Pharmaceutica N.V. | Synergistic antifungal ddac compositions |
| EP1563731A1 (en) | 2004-02-12 | 2005-08-17 | Bayer CropScience S.A. | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the ergosterol biosynthesis |
| EP1570737A1 (en) * | 2004-02-12 | 2005-09-07 | Bayer CropScience S.A. | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the methionine biosynthesis |
| GB0508993D0 (en) | 2005-05-03 | 2005-06-08 | Syngenta Participations Ag | Pesticidal compositions |
| EP2015637B1 (en) | 2006-05-02 | 2011-07-13 | Janssen Pharmaceutica N.V. | Biocidal combinations comprising imazalil |
| CL2007001970A1 (es) * | 2006-07-06 | 2008-04-18 | Bayer Cropscience Ag | Composicion farmaceutica que comprende un derivado de piridiletilbenzamida y un compuesto insecticida; y un metodo para controlar de forma preventiva o curativa hongos e insectos fitopatogenos. |
| US20080039431A1 (en) * | 2006-08-08 | 2008-02-14 | Cleary Charles L | Method of improving plant growth by reducing viral infections |
| US20100035753A1 (en) * | 2007-02-05 | 2010-02-11 | Basf Se | Fungicidal Mixtures Comprising Substituted 1-methylpyrazol-4-ylcarboxanilides |
| EP2011395A1 (en) * | 2007-07-03 | 2009-01-07 | Bayer CropScience AG | Active compound combinations |
| EP2036438A1 (en) * | 2007-09-12 | 2009-03-18 | Bayer CropScience AG | Post-harvest treatment |
| UA106483C2 (uk) * | 2009-01-30 | 2014-09-10 | ะะฐะนะตั ะัะพะฟัะฐะนะตะฝั ะะณ | ะะฐััะพััะฒะฐะฝะฝั ัะฝะณัะฑััะพััะฒ ััะบัะธะฝะฐัะดะตะณัะดัะพะณะตะฝะฐะทะธ ะดะปั ะฑะพัะพััะฑะธ ะทั ัะฟัะฐะฒะถะฝัะพั ะฑะพัะพัะฝะธััะพั ัะพัะพั ัะบ ะฟะตัะฒะธะฝะฝะพั ัะฝัะตะบัััั |
| JP5484490B2 (ja) * | 2009-03-12 | 2014-05-07 | ใใผใจใผใจในใจใ ใฝใทใจใฟในใปใจใผใญใใข | ใใซใชใใฉใ ๏ผ๏ผฆ๏ฝ๏ฝ๏ฝ๏ฝ๏ฝ๏ฝ๏ฝ๏ฝ๏ผๅใณ๏ผโใจใใซโ๏ผโใชใฏใใซโ๏ผป๏ผ๏ผ๏ผ๏ผ๏ผ๏ผฝใใชใขใพใญ๏ผป๏ผ๏ผ๏ผโ๏ฝ๏ผฝใใชใใธใณโ๏ผโใคใซใขใใณใๅซใๆฎบ่็ตๆ็ฉ |
| CN102348380B (zh) | 2009-03-16 | 2013-10-23 | ๅทดๆฏๅคซๆฌงๆดฒๅ ฌๅธ | ๅ ๅซๆฐๅก่้ ฐ่บๅ่ฏ่้ ฎ็ๆ็่็ปๅ็ฉ |
| CA2763835C (en) * | 2009-06-02 | 2017-01-31 | Bayer Cropscience Ag | Use of succinate dehydrogenase inhibitors for controlling sclerotinia spp. |
| CN101803606B (zh) * | 2010-02-05 | 2013-05-08 | ๅฑฑไธ็่ฑ็็ ็ฉถๆ | ่ฑ็้ปๆ็ ๅ่คๆ็ ็้ฒๆฒปๆทท้ ่ฏๅๅๅ ถไฝฟ็จๆนๆณ |
| CN102450265A (zh) * | 2010-10-14 | 2012-05-16 | ๆตทๅฉๅฐ่ฏไธ้ๅข่กไปฝๆ้ๅ ฌๅธ | ไธ็งๅซๆฐๅก่้ ฐ่บๅไธ็ฏๅ็ๆ่็ปๅ็ฉ |
| CN101961021A (zh) * | 2010-11-05 | 2011-02-02 | ้ๅฒๆตทๅฉๅฐ่ฏไธๆ้ๅ ฌๅธ | ไธ็งๅซๆๆฐๅก่้ ฐ่บ็ๆ่็ปๅ็ฉ |
| AR083922A1 (es) | 2010-11-22 | 2013-04-10 | Bayer Cropscience Lp | Procedimientos para prevenir y/o tratar enfermedades fungicas o nematodos, tales como el sindrome de muerte subita (sds) |
| CN102027934A (zh) * | 2010-11-26 | 2011-04-27 | ๆ ๅทๅธไธญ่ฟ ๅๅทฅๆ้ๅ ฌๅธ | ไธ็งๅซๆๆฐๅก่้ ฐ่บๅ่ฏ้็ฒ็ฏๅ็ๆ่็ปๅ็ฉๅๅ ถๅบ็จ |
| BR122019014555B1 (pt) * | 2011-01-28 | 2022-03-22 | Deepak Pranjivandas Shah | Composiรงรฃo pesticida de enxofre e fungicidas |
| AR085587A1 (es) * | 2011-04-13 | 2013-10-09 | Bayer Cropscience Ag | Combinaciones de compuestos activos |
| US20130045968A1 (en) * | 2011-08-15 | 2013-02-21 | Norman Helie | Plant treatment |
| DE102011117895A1 (de) * | 2011-11-04 | 2013-05-08 | Sourcon-Padena Gmbh & Co. Kg | Behandlung und/oder Prophylaxe von Lagerkrankheiten bei Erntegut |
| EP2612554A1 (en) | 2012-01-09 | 2013-07-10 | Bayer CropScience AG | Fungicide compositions comprising fluopyram, at least one succinate dehydrogenase (SDH) inhibitor and optionally at least one triazole fungicide |
| CN103535365A (zh) * | 2012-07-11 | 2014-01-29 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๆ่็ปๅ็ฉ |
| CN104285998A (zh) * | 2012-07-11 | 2015-01-21 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๆ่็ปๅ็ฉ |
| CN104285954B (zh) * | 2012-07-13 | 2016-08-24 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๆ่็ปๅ็ฉ |
| CN103651413B (zh) * | 2012-09-21 | 2015-09-09 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๆฐๅๆดปๅ้ ฏไธไธๅ็ฑป็ๆ่็ปๅ็ฉ |
| CN104839175B (zh) * | 2012-09-26 | 2017-01-18 | ้่ฅฟ็พ้ฆๅ่ฏๆ้ๅ ฌๅธ | ไธ็งๅซๆฐๅๆดปๅ้ ฏไธไธๅ็ฑป็ๆ่็ปๅ็ฉ |
| US9750248B2 (en) * | 2012-12-31 | 2017-09-05 | Dow Agrosciences Llc | Synergistic fungicidal compositions |
| CN105265438A (zh) * | 2014-05-27 | 2016-01-27 | ๆทฑๅณ่ฏบๆฎไฟกๅๅ่กไปฝๆ้ๅ ฌๅธ | ไธ็งๆ่็ปๅ็ฉ |
| EA201692523A1 (ru) * | 2014-06-11 | 2017-05-31 | ะะฐะนะตั ะัะพะฟัะฐะนะตะฝั ะะบัะธะตะฝะณะตะทะตะปััะฐัั | ะะพะผะฑะธะฝะฐัะธะธ ะฐะบัะธะฒะฝัั ัะพะตะดะธะฝะตะฝะธะน, ะฒะบะปััะฐััะธะต ะฟัะพะบะฒะธะฝะฐะทะธะด ะธ ัะฟะธัะพะบัะฐะผะธะฝ ะธ, ะฝะตะพะฑัะทะฐัะตะปัะฝะพ, ะฟัะพัะธะพะบะพะฝะฐะทะพะป |
| CN104170829A (zh) * | 2014-09-01 | 2014-12-03 | ๅฑฑไธ็ขงๅฅฅ็็ฉ็งๆๆ้ๅ ฌๅธ | ไธ็งๅซๆฐๅก่้ ฐ่บๅ่ฏ้็ฒ็ฏๅ็ๅ่ฏ็ปๅ็ฉ |
| UY36432A (es) * | 2014-12-16 | 2016-06-30 | Bayer Cropscience Ag | Combinaciones de compuestos activos que comprenden un derivado de (tio) carboxamida y compuesto(s) fungicida(s) |
| JP2018503676A (ja) | 2015-01-27 | 2018-02-08 | ใใผใใปใชใใปใชใผใธใจใณใ๏ผใถใปใฆใใใผใทใใคใปใชใใปใใญใตในใปใทในใใ | ็ ๅ็่ใซๆๆใใๆค็ฉใๅฆ็ใใใฎใซๆๅนใชๆฎบ่ๅคไฟ้ฒๅค |
| CN104872141A (zh) * | 2015-05-25 | 2015-09-02 | ๅนฟไธไธญ่ฟ ๅ็ง่กไปฝๆ้ๅ ฌๅธ | ไธ็งๅซๆ็ญ่ๅๅๆฐๅก่้ ฐ่บ็ๆ่็ปๅ็ฉ |
| CN106259346B (zh) * | 2016-08-20 | 2018-12-14 | ๆฑ่ๅบทๅทด็น็็ฉๅทฅ็จๆ้ๅ ฌๅธ | ไธ็งๅซๆฐๅก่้ ฐ่บๅ่ถ็็ด ็ๆ็บฟ่ซ็ปๅ็ฉ |
| CN106538547A (zh) * | 2016-10-13 | 2017-03-29 | ๆทฑๅณ่ฏบๆฎไฟกๅๅ่กไปฝๆ้ๅ ฌๅธ | ๆ่็ปๅ็ฉๅๅ ถๅบ็จ |
| CN106857534A (zh) * | 2017-03-23 | 2017-06-20 | ้่ฅฟไธๆ ผไน่ทฏ็็ฉ็งๅญฆๆ้ๅ ฌๅธ | ไธ็งๅซๆๆฐๅก่้ ฐ่บๅๅง้่บ็ๆ่็ปๅ็ฉ |
| CN108077270A (zh) * | 2017-12-14 | 2018-05-29 | ้่ฅฟไธๆ ผไน่ทฏ็็ฉ็งๅญฆๆ้ๅ ฌๅธ | ไธ็งๅซๆๆฐๅก่้ ฐ่บๅ็ฏ้ ฐ่่บ็ๆ่็ปๅ็ฉ |
| CN109182143B (zh) * | 2018-09-28 | 2021-09-24 | ๆฒณๅๅไธๅคงๅญฆ | ไธ็ง็ๆฒ้lsd-1ๅๅ ถๅนๅ ปๆนๆณๅๅบ็จ |
| WO2020231751A1 (en) | 2019-05-10 | 2020-11-19 | Bayer Cropscience Lp | Active compound combinations |
| CN115943962B (zh) * | 2023-01-05 | 2024-06-25 | ๆฒณๅ็งๆๅญฆ้ข | ไธ็ง้ฒๆฒปๅฐ้บฆ็บนๆฏ็ ็ๆ่็ปๅ็ฉ |
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- 2005-02-10 CN CN2005800042164A patent/CN1917760B/zh not_active Expired - Lifetime
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- 2005-02-10 WO PCT/EP2005/002568 patent/WO2005077183A1/en not_active Ceased
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- 2005-02-10 KR KR1020067016372A patent/KR100838541B1/ko not_active Expired - Lifetime
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- 2006-09-08 MA MA29310A patent/MA28460B1/fr unknown
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- 2012-03-26 US US13/430,477 patent/US9433213B2/en not_active Expired - Fee Related
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