AR086961A1 - Mezclas fungicidas sinergicas que comprenden 2,3,5,6-tetraciano-[1,4]ditiina - Google Patents
Mezclas fungicidas sinergicas que comprenden 2,3,5,6-tetraciano-[1,4]ditiinaInfo
- Publication number
- AR086961A1 AR086961A1 ARP120102146A ARP120102146A AR086961A1 AR 086961 A1 AR086961 A1 AR 086961A1 AR P120102146 A ARP120102146 A AR P120102146A AR P120102146 A ARP120102146 A AR P120102146A AR 086961 A1 AR086961 A1 AR 086961A1
- Authority
- AR
- Argentina
- Prior art keywords
- fluquinconazole
- methyl
- inhibitors
- phenyl
- pyrazol
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 5
- 239000000417 fungicide Substances 0.000 title abstract 4
- 230000000855 fungicidal effect Effects 0.000 title 1
- 230000002195 synergetic effect Effects 0.000 title 1
- 239000005785 Fluquinconazole Substances 0.000 abstract 32
- 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 abstract 32
- -1 coumethoxystrobin Chemical compound 0.000 abstract 29
- 239000003112 inhibitor Substances 0.000 abstract 20
- 230000015572 biosynthetic process Effects 0.000 abstract 7
- 241000223260 Trichoderma harzianum Species 0.000 abstract 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 4
- 238000003786 synthesis reaction Methods 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 abstract 3
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 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 abstract 2
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 abstract 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 abstract 2
- 244000063299 Bacillus subtilis Species 0.000 abstract 2
- 235000014469 Bacillus subtilis Nutrition 0.000 abstract 2
- 241000896542 Clonostachys rosea f. catenulata Species 0.000 abstract 2
- 102000015782 Electron Transport Complex III Human genes 0.000 abstract 2
- 108010024882 Electron Transport Complex III Proteins 0.000 abstract 2
- 241000196324 Embryophyta Species 0.000 abstract 2
- 241000233866 Fungi Species 0.000 abstract 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 abstract 2
- 229930182764 Polyoxin Natural products 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 241000223261 Trichoderma viride Species 0.000 abstract 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 abstract 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 abstract 2
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 abstract 2
- 230000032823 cell division Effects 0.000 abstract 2
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 abstract 2
- 229930195729 fatty acid Natural products 0.000 abstract 2
- 239000000194 fatty acid Substances 0.000 abstract 2
- 150000004665 fatty acids Chemical class 0.000 abstract 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 abstract 2
- 150000002632 lipids Chemical class 0.000 abstract 2
- 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 abstract 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 2
- 150000003904 phospholipids Chemical class 0.000 abstract 2
- 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 abstract 2
- 230000029058 respiratory gaseous exchange Effects 0.000 abstract 2
- 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 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 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 abstract 2
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A 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-CSLFJTBJSA-N 0.000 abstract 2
- 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- CXNPLSGKWMLZPZ-GIFSMMMISA-N (2r,3r,6s)-3-[[(3s)-3-amino-5-[carbamimidoyl(methyl)amino]pentanoyl]amino]-6-(4-amino-2-oxopyrimidin-1-yl)-3,6-dihydro-2h-pyran-2-carboxylic acid Chemical compound O1[C@@H](C(O)=O)[C@H](NC(=O)C[C@@H](N)CCN(C)C(N)=N)C=C[C@H]1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-GIFSMMMISA-N 0.000 abstract 1
- 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 abstract 1
- 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 abstract 1
- CJRQLBCPVAPJRS-UHFFFAOYSA-N (8-benzyl-2,3-dioxo-1,5-dioxonan-7-yl) 2-methylpropanoate Chemical compound CC(C)C(=O)OC1COCC(=O)C(=O)OCC1CC1=CC=CC=C1 CJRQLBCPVAPJRS-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- HILAYQUKKYWPJW-UHFFFAOYSA-N 1-dodecylguanidine Chemical compound CCCCCCCCCCCCN=C(N)N HILAYQUKKYWPJW-UHFFFAOYSA-N 0.000 abstract 1
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 abstract 1
- NFTOEHBFQROATQ-UHFFFAOYSA-N 2,3-dihydrofuran-5-carboxylic acid Chemical compound OC(=O)C1=CCCO1 NFTOEHBFQROATQ-UHFFFAOYSA-N 0.000 abstract 1
- DFPIGVDNBRPLIL-UHFFFAOYSA-N 2,3-dimethyl-5-(4-methylphenyl)-3-pyridin-3-yl-1,2-oxazolidine Chemical compound CN1OC(C=2C=CC(C)=CC=2)CC1(C)C1=CC=CN=C1 DFPIGVDNBRPLIL-UHFFFAOYSA-N 0.000 abstract 1
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- QKJJCZYFXJCKRX-HZHKWBLPSA-N 2-[(2s,3s,6r)-6-[4-amino-5-(hydroxymethyl)-2-oxopyrimidin-1-yl]-3-[[(2s)-2-amino-3-hydroxypropanoyl]amino]-3,6-dihydro-2h-pyran-2-yl]-5-(diaminomethylideneamino)-2,4-dihydroxypentanoic acid Chemical compound O1[C@H](C(O)(CC(O)CN=C(N)N)C(O)=O)[C@@H](NC(=O)[C@H](CO)N)C=C[C@@H]1N1C(=O)N=C(N)C(CO)=C1 QKJJCZYFXJCKRX-HZHKWBLPSA-N 0.000 abstract 1
- 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 abstract 1
- OWDLFBLNMPCXSD-UHFFFAOYSA-N 2-chloro-N-(2,6-dimethylphenyl)-N-(2-oxotetrahydrofuran-3-yl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)C1C(=O)OCC1 OWDLFBLNMPCXSD-UHFFFAOYSA-N 0.000 abstract 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 abstract 1
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- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 abstract 1
- 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- ZGBKIRCRHOIXAN-UHFFFAOYSA-N 5-chloro-1-(4,6-dimethoxypyrimidin-2-yl)-2-methylbenzimidazole Chemical compound COC1=CC(OC)=NC(N2C3=CC=C(Cl)C=C3N=C2C)=N1 ZGBKIRCRHOIXAN-UHFFFAOYSA-N 0.000 abstract 1
- NEKULYKCZPJMMJ-UHFFFAOYSA-N 5-chloro-N-{1-[4-(difluoromethoxy)phenyl]propyl}-6-methylpyrimidin-4-amine Chemical compound C=1C=C(OC(F)F)C=CC=1C(CC)NC1=NC=NC(C)=C1Cl NEKULYKCZPJMMJ-UHFFFAOYSA-N 0.000 abstract 1
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- FKWDSATZSMJRLC-UHFFFAOYSA-N Iminoctadine acetate Chemical compound CC([O-])=O.CC([O-])=O.CC([O-])=O.NC([NH3+])=NCCCCCCCC[NH2+]CCCCCCCCN=C(N)[NH3+] FKWDSATZSMJRLC-UHFFFAOYSA-N 0.000 abstract 1
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- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 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 abstract 1
- 229960000625 oxytetracycline Drugs 0.000 abstract 1
- 235000019366 oxytetracycline Nutrition 0.000 abstract 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 abstract 1
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical class OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 abstract 1
- 230000035699 permeability Effects 0.000 abstract 1
- 238000005502 peroxidation Methods 0.000 abstract 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 abstract 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 abstract 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 abstract 1
- 125000005543 phthalimide group Chemical class 0.000 abstract 1
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- 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 abstract 1
- 150000004885 piperazines Chemical class 0.000 abstract 1
- 230000004260 plant-type cell wall biogenesis Effects 0.000 abstract 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 abstract 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 abstract 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 abstract 1
- 239000012268 protein inhibitor Substances 0.000 abstract 1
- 229940121649 protein inhibitor Drugs 0.000 abstract 1
- 239000000007 protein synthesis inhibitor Substances 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 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 abstract 1
- JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 150000003222 pyridines Chemical class 0.000 abstract 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000003230 pyrimidines Chemical class 0.000 abstract 1
- 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 abstract 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 abstract 1
- 230000019491 signal transduction Effects 0.000 abstract 1
- CCCGEKHKTPTUHJ-ZJUUUORDSA-N solatenol Chemical compound C1([C@]2([H])CC[C@]3(C2=C(Cl)Cl)[H])=C3C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F CCCGEKHKTPTUHJ-ZJUUUORDSA-N 0.000 abstract 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 abstract 1
- 150000003432 sterols Chemical class 0.000 abstract 1
- 235000003702 sterols Nutrition 0.000 abstract 1
- 229960005322 streptomycin Drugs 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 229940124530 sulfonamide Drugs 0.000 abstract 1
- 150000003456 sulfonamides Chemical class 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- 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 abstract 1
- LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 abstract 1
- 239000004308 thiabendazole Substances 0.000 abstract 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 abstract 1
- 235000010296 thiabendazole Nutrition 0.000 abstract 1
- 229960004546 thiabendazole Drugs 0.000 abstract 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 abstract 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 abstract 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- 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 abstract 1
- 150000003852 triazoles Chemical class 0.000 abstract 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 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 abstract 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 abstract 1
- 239000003744 tubulin modulator Substances 0.000 abstract 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 abstract 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 abstract 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 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
- A01N43/24—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
- 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
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- A01N43/52—1,3-Diazoles; Hydrogenated 1,3-diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A01N43/72—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)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Cultivation Of Plants (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Uso de estas mezclas para combatir hongos fitopatógenos y semillas recubiertas con al menos una de esas mezclas. También, métodos para combatir hongos dañinos usando tales mezclas.Reivindicación 1: Una mezcla, caracterizada porque comprende, como componentes activos: i) al menos un compuesto de la fórmula (1), en donde: k indica la cantidad de átomos de oxígeno unidos a un átomo de azufre del resto de ditiína y k es 0 ó 1; siendo los cuatro sustituyentes R idénticos; R es CN y ii) al menos un compuesto activo II seleccionado de los grupos A) a O): A) Inhibidores de la respiración: Inhibidores del complejo III en el sitio Qo (por ejemplo, estrobilurinas): azoxistrobina, coumetoxistrobina, coumoxistrobina, dimoxistrobina, enestroburina, fenaminstrobina, fenoxistrobina/flufenoxistrobina fluoxastrobina, cresoxim-metilo, metominostrobina, orisastrobina, picoxistrobina, piraclostrobina, pirametostrobina, piraoxistrobina, trifloxistrobina, éster metílico de ácido 2-[2-(2,5-dimetil-fenoximetil)-fenil]3-metoxi-acrílico y 2-(2-(3-(2,6-diclorofenil)-1-metil-alilidenaminooximetil)-fenil)-2-metoxiimino-N-metil-acetamida, piribencarb, triclopiricarb/clorodincarb, famoxadona, fenamidona; Inhibidores del complejo III en el sitio Qi: ciazofamida, amisulbromo, 2-metilpropanoato de [(3S,6S,7R,8R)-8-bencil-3-[(3acetoxi-4-metoxi-piridin-2-carbonil)amino]-6-metil-4,9-dioxo-1,5-dioxonan-7-ilo], 2-metilpropanoato de [(3S,6S,7R,8R)-8-bencil-3-[[3-(acetoximetoxi)-4-metoxi-piridin-2-carbonil]amino]-6-metil-4,9-dioxo-1,5-dioxonan-7-ilo], 2-metilpropanoato de [(3S,6S,7R,8R)-8-benciI-3-[(3-isobutoxicarboniloxi-4-metoxipiridin-2-carbonil)amino]-6-metil-4,9-dioxo-1,5-dioxonan-7-ilo], 2-metilpropanoato de [(3S,6S,7R,8R)-8-bencil-3-[[3-(1,3-benzodioxol-5-ilmetoxi)-4-metoxi-piridin-2-carbonil]amino]-6-metil-4,9-dioxo-1,5-dioxonan-7-ilo], 2-metilpropanoato de dioxo-8-(fenilmetil)-1,5-dioxonan-7-ilo; Inhibidores de complejo II (por ejemplo, carboxamidas): benodanilo, bixafeno, boscalida, carboxina, fenfuram, fluopiram, flutolanilo, fluxapiroxad, furametpir, isopirazam, mepronilo, oxicarboxina, penflufeno, pentiopirad, sedaxano, tecloftalam, tifluzamida, N-(4’-trifluorometiltiobifenil-2-il)-3-difluorometil-1-metil-1H-pirazol-4-carboxamida, N-(2-(1,3,3-trimetil-butil)-fenil)-1,3-dimetil-5-fluoro-1H-pirazol-4-carboxamida, N-[9-(diclorometilen)-1,2,3,4-tetrahidro-1,4-metanonaftalen-5-il]-3-(difluorometil)-1-metil-1H-pirazol-4-carboxamida; Otros inhibidores de la respiración (por ejemplo, complejo I, desacopladores): diflumetorim, (5,8-difluoroquinazolin-4-il)-{2-[2-fIuoro-4-(4-trifIuorometiIpiridin-2-iloxi)-fenil]-etil}-amina; derivados de nitrofenilo: binapacrilo, dinobutona, dinocap, fluazinam; ferimzona; compuestos organometálicos: sales de fentina, tales como acetato de fentina, cloruro de fentina o hidróxido de fentina; ametoctradina; y siltiofam; B) Inhibidores de la biosíntesis de esterol (fungicidas SBI): Inhibidores de C14 demetilasa (fungicidas DMI): triazoles: azaconazol, bitertanol, bromuconazol, ciproconazol, difenoconazol, diniconazol, diniconazol-M, epoxiconazol, fenbuconazol, fluquinconazol, flusilazol, flutriafol, hexaconazol, imibenconazol, ipconazol, metconazol, miclobutanilo, oxpoconazol, paclobutrazol, penconazol, propiconazol, protioconazol, simeconazol, tebuconazol, tetraconazol, triadimefona, triadimenol, triticonazol, uniconazol, 1-[rel-(2S;3R)-3-(2-clorofenil)-2-(2,4-difluorofenil)-oxiranilmetil]-5-tiocianato-1H-[1,2,4]triazol, 2-[rel-(2S;3R)-3-(2-clorofenil)-2-(2,4-difluorofenil)-oxiranilmetil]-2H-[1,2,4]triazol-3-tiol; imidazoles: imazalilo, pefurazoato, procloraz, triflumizol; pirimidinas, piridinas y piperazinas: fenarimol, nuarimol, pirifenox, triforina; Inhibidores de D14-reductasa: aldimorf, dodemorf, acetato de dodemorf, fenpropimorf, tridemorf, fenpropidina, piperalina, espiroxamina; Inhibidores de 3-cetorreductasa: fenhexamida; C) Inhibidores de la síntesis de ácido nucleico: Fungicidas de fenilamidas o aminoácido de acilo: benalaxilo, benalaxil-M, kiralaxilo, metalaxilo, metalaxil-M (mefenoxam), ofurace, oxadixilo; Otros: himexazol, octilinona, ácido oxolínico, bupirimato, 5-fluorocitosina, 5-fluoro-2-(p-tolilmetoxi)pirimidin-4-amina, 5-fluoro-2-(4-fluorofenilmetoxi)pirimidin-4-amina; D) Inhibidores de la división celular y del citoesqueleto: Inhibidores de tubulina, tales como bencimidazoles, tiofanatos: benomilo, carbendazim, fuberidazol, tiabendazol, tiofanato-metilo; triazolopirimidinas: 5-cloro-7-(4-metilpiperidin-1-iI)-6-(2,4,6-trifluorofenil)-[1,2,4]triazolo[1,5-a]pirimidina; Otros inhibidores de la división celular: dietofencarb, etaboxam, pencicurona, fluopicolida, zoxamida, metrafenona, piriofenona; E) Inhibidores de la síntesis de aminoácidos y proteínas: Inhibidores de la síntesis de metionina (anilino-pirimidinas): ciprodinilo, mepanipirim, pirimetanilo; Inhibidores de la síntesis de proteínas: blasticidina-S, kasugamicina, clohidratohidrato de casugamicina, mildiomicina, estreptomicina, oxitetraciclina, polioxina, validamicina A; F) Inhibidores de la transducción de señales: Inhibidores de la MAP / histidina quinasa: fluoroimida, iprodiona, procimidona, vinclozolina, fenpiclonilo, fludioxonilo; Inhibidores de la proteína G; quinoxifeno; G) Inhibidores de la síntesis de lípidos y membrana: Inhibidores de la biosíntesis de fosfolípidos: edifenfos, iprobenfos, pirazofos, isoprotiolano; Peroxidación de lípidos: diclorano, quintoceno, tecnaceno, tolclofos-metilo, bifenilo, cloroneb, etridiazol; Biosíntesis de fosfolípidos y deposición de la pared celular: dimetomorf, flumorf, mandipropamida, pirimorf, bentiavalicarb, iprovalicarb, valifenalato y éster (4-fluorofenílico) del ácido N-(1-(1-(4-ciano-fenil)etansulfonil)-but-2-il) carbámico; Compuestos que afectan la permeabilidad de la membrana celular y los ácidos grasos: propamocarb, clorhidrato de propamocarb; Inhibidores de amidahidrolasa de ácidos grasos: 1-[4-[4-[5-(2,6-difluorofenil)-4,5-dihidro-3-isoxazolil]-2-tiazolil]-1-piperidinil]-2-[5-metil-3-(trifluorometil)-1H-pirazol-1-il]etanona; H) Inhibidores con acción multisitio: Sustancias activas inorgánicas: mezcla de Bordeaux, acetato de cobre, hidróxido de cobre, oxicloruro de cobre, sulfato de cobre básico, azufre; Tio- y ditiocarbamatos: ferbam, mancozeb, maneb, metam, metiram, propineb, tiram, zineb, ziram; Compuestos de organocloro (por ejemplo, ftalimidas, sulfamidas, cloronitrilos): anilazina, clorotalonilo, captafol, captano, folpet, diclofluanida, diclorofeno, flusulfamida, hexaclorobenceno, pentaclorofenoles y sus sales, ftalida, tolilfluanida, N-(4-cloro-2-nitro-fenil)-N-etil-4-metil-bencensulfonamida; Guanidinas y otros: guanidina, dodina, base libre de dodina, guazatina, acetato de guazatina, iminoctadina, triacetato de iminoctadina, tris(albesilato) de iminoctadina, ditianona, 2,6-dimetil-1H,5H-[1,4]ditiino[2,3-c:5,6-c’]dipirrol-1,3,5,7(2H,6H)-tetraona; I) Inhibidores de la síntesis de la pared celular: Inhibidores de la síntesis de glucano: validamicina, polioxina B; inhibidores de la síntesis de melanina: piroquilona, triciclazol, carpropamida, diciclomet, fenoxanilo; J) Inducidores de la defensa de la planta: acibenzolar-S-metilo, probenazol, isotianilo, tiadinilo, prohexadiona-calcio; fosfonatos: fosetilo, fosetil-aluminio, ácido fosforoso y sus sales; K) Modo de acción desconocido: bronopol, quinometionato, ciflufenamida, cimoxanilo, dazomet, debacarb, diclomezina, difenzoquat, metilsulfato de difenzoquat, difenilamina, fenpirazamina, flumetover, flusulfamida, flutianilo, metasulfocarb, nitrapirina, nitrotal-isopropilo, oxina-cobre, proquinazida, tebufloquina, tecloftalam, triazóxido, 2-butoxi-6-yodo-3-propilcromen-4-ona, N-(ciclopropilmetoxiimino-(6-difluoro-metoxi-2,3-difluoro-fenil)-metil)-2-fenilacetamida, N’-(4-(4-cloro-3-trifluorometil-fenoxi)-2,5-dimetil-fenil)-N-etil-N-metilformamidina, N’-(4-(4-fluoro-3-trifluorometil-fenoxi)-2,5dimetil-fenil)-N-etil-N-metilformamidina, N’-(2-metil-5-trifluorometil-4-(3-trimetiIsilaniI-propoxi)-fenil)-N-etil-N-metilformamidina, N’-(5-difluorometil-2-metil-4-(3-trimetilsilanil-propoxi)-fenil)-N-etil-N-metilformamidina, metil-(1,2,3,4-tetrahidro-naftalen-1-il)-amida del ácido 2-{1-[2-(5-metil-3-trifluorometil-pirazol-1-il)-acetil]-piperidin-4-il}-tiazoI-4-carboxílico, metil-(R)1,2,3,4-tetrahidro-naftalen-1-il-amida del ácido 2-{1-[2-(5-metil-3-trifluorometil-pirazol-1-il)-acetil]-piperidin-4-il}-tiazoI-4-carboxílico, 1-[4-[4-[5-(2,6-difluorofenil)-4,5-dihidro-3-isoxazolil]2-tiazolil]1-piperidinil]-2-[5-metil-3-(trifluorometil)-1H-pirazol-1-il]etanona, éster 6-ter-butil-8-fluoro-2,3-dimetil-quinolin-4-ílico del ácido metoxi-acético, N-metil-2-{1-[(5-metil-3-trifluorometil-1H-pirazol-1-il)-acetil]-piperidin-4-il}-N-[(1R)-1,2,3,4-tetrahidronaftalen-1-il]-4-tiazolcarboxamida, 3-[5-(4-metilfenil)-2,3-dimetil-isoxazolidin-3-il]-piridina, 3-[5-(4-cloro-fenil)-2,3-dimetil-isoxazolidin-3-il-]piridina (pirisoxazol), amida del ácido N-(6-metoxi-piridin-3-iI)ciclopropancarboxílico, 5-cloro-1-(4,6-dimetoxi-pirimidin-2-il)-2-metil-1H-benzoimidazol, 2-(4-cloro-fenil)-N-[4-(3,4-dimetoxi-fenil)-isoxazol-5-il]-2-prop-2-iniloxi-acetamida; L) Agentes de biocontrol antifúngicos, bioactivadores de plantas: Ampelomyces quisqualis, Aspergillus flavus, Aureobasidium pullulans, Bacillus pumilus, Bacillus subtilis, Bacillus subtilis var. amyloliquefaciens FZB24, Candida saitoana, Clonostachys rosea f. catenulata, también denominado Gliocladium catenulatum, Coniothyrium minitans, Cryphonectria parasitica, Cryptococcus albidus, Fusarium oxysporum, Metschnikowia fructicola, Microdochium dimerum, Phlebiopsis gigantea, Pseudozyma flocculosa, Pythium oligandrum DV74, Reynoutria sachlinensis, Talaromyces flavus V117b, Trichoderma asperellum SKT-1, T. atroviride LC52, T. harzianum T-22, T. harzianum TH 35, T. harzianum T-39, T. harzianum y T. viride, T. harzianum ICC012 y T. viride ICC080, T. polysporum y T. harzianum, T. stromaticum,
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| WO2005087773A1 (de) | 2004-03-10 | 2005-09-22 | Basf Aktiengesellschaft | 5,6-dialkyl-7-amino-triazolopyrimidine, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel |
| BRPI0508337A (pt) | 2004-03-10 | 2007-07-24 | Basf Ag | compostos, processos para a preparação dos mesmos, agente fungicida, semente, e, processo para o combate de fungos nocivos fitopatogênicos |
| KR20070039026A (ko) | 2004-06-03 | 2007-04-11 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 아미디닐페닐 화합물의 살진균성 혼합물 |
| BRPI0512121A (pt) | 2004-06-18 | 2008-02-06 | Basf Ag | composto, processo para combater fungos nocivos, agente fungicida, e, uso de compostos |
| EP1761498A1 (de) | 2004-06-18 | 2007-03-14 | Basf Aktiengesellschaft | 1-methyl-3-difluormethyl-pyrazol-4-carbonsäure-(ortho-phenyl)-anilide und ihre verwendung als fungizid |
| GB0418048D0 (en) | 2004-08-12 | 2004-09-15 | Syngenta Participations Ag | Method for protecting useful plants or plant propagation material |
| ES2308726T3 (es) | 2005-02-16 | 2008-12-01 | Basf Se | 5-alcoxiaquil-6-alquil-7-amino-azolopirimidinas, procedimiento para su obtencion y su empleo para la lucha contra hongos dañinos asi como agentes que las contienen. |
| DE102005007160A1 (de) | 2005-02-16 | 2006-08-24 | Basf Ag | Pyrazolcarbonsäureanilide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen |
| DE102005009458A1 (de) | 2005-03-02 | 2006-09-07 | Bayer Cropscience Ag | Pyrazolylcarboxanilide |
| RU2428416C2 (ru) | 2006-01-13 | 2011-09-10 | Дау Агросайенсиз Ллс | 6-(полизамещенный арил)-4-аминопиколинаты и их применение в качестве гербицидов |
| US8124565B2 (en) | 2006-02-09 | 2012-02-28 | Syngenta Crop Protection, Inc. | Method of protecting a plant propagation material, a plant, and/or plant organs |
| EA019396B1 (ru) | 2009-09-01 | 2014-03-31 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Синергическая фунгицидная композиция, содержащая производное 5-фторпиримидина для борьбы с грибками у злаков |
| AR077956A1 (es) * | 2009-09-14 | 2011-10-05 | Bayer Cropscience Ag | Combinaciones de compuestos activos |
| PL2706058T3 (pl) * | 2010-04-14 | 2016-01-29 | Bayer Ip Gmbh | Pochodne ditiiny jako środki grzybobójcze |
-
2012
- 2012-06-15 KR KR1020147000970A patent/KR20140040223A/ko not_active Withdrawn
- 2012-06-15 EA EA201400027A patent/EA201400027A1/ru unknown
- 2012-06-15 AR ARP120102146A patent/AR086961A1/es not_active Application Discontinuation
- 2012-06-15 UY UY0001034136A patent/UY34136A/es unknown
- 2012-06-15 BR BR112013030476A patent/BR112013030476A2/pt not_active IP Right Cessation
- 2012-06-15 CA CA2836020A patent/CA2836020A1/en not_active Abandoned
- 2012-06-15 CN CN201280029827.4A patent/CN103607890A/zh active Pending
- 2012-06-15 US US14/126,644 patent/US20140121103A1/en not_active Abandoned
- 2012-06-15 MX MX2013013239A patent/MX2013013239A/es not_active Application Discontinuation
- 2012-06-15 WO PCT/EP2012/061469 patent/WO2012172061A1/en not_active Ceased
- 2012-06-15 AU AU2012268976A patent/AU2012268976A1/en not_active Abandoned
- 2012-06-15 EP EP12728506.2A patent/EP2720541A1/en not_active Withdrawn
- 2012-06-15 JP JP2014515211A patent/JP2014518208A/ja active Pending
-
2013
- 2013-11-19 IL IL229499A patent/IL229499A0/en unknown
- 2013-11-26 CR CR20130622A patent/CR20130622A/es unknown
-
2014
- 2014-01-15 ZA ZA2014/00313A patent/ZA201400313B/en unknown
- 2014-01-16 CO CO14007812A patent/CO6852077A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU2012268976A1 (en) | 2014-01-16 |
| KR20140040223A (ko) | 2014-04-02 |
| CO6852077A2 (es) | 2014-01-30 |
| CN103607890A (zh) | 2014-02-26 |
| EA201400027A1 (ru) | 2014-04-30 |
| MX2013013239A (es) | 2014-01-08 |
| BR112013030476A2 (pt) | 2017-06-20 |
| WO2012172061A1 (en) | 2012-12-20 |
| CR20130622A (es) | 2014-02-28 |
| JP2014518208A (ja) | 2014-07-28 |
| ZA201400313B (en) | 2015-06-24 |
| IL229499A0 (en) | 2014-01-30 |
| CA2836020A1 (en) | 2012-12-20 |
| EP2720541A1 (en) | 2014-04-23 |
| US20140121103A1 (en) | 2014-05-01 |
| UY34136A (es) | 2013-01-03 |
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| FA | Abandonment or withdrawal |