AR077183A1 - Combinaciones de levaduras con actividad fungicida y fungicidas - Google Patents
Combinaciones de levaduras con actividad fungicida y fungicidasInfo
- Publication number
- AR077183A1 AR077183A1 ARP100102190A ARP100102190A AR077183A1 AR 077183 A1 AR077183 A1 AR 077183A1 AR P100102190 A ARP100102190 A AR P100102190A AR P100102190 A ARP100102190 A AR P100102190A AR 077183 A1 AR077183 A1 AR 077183A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- phenyl
- inhibitors
- carboxamide
- ethyl
- Prior art date
Links
- 239000000417 fungicide Substances 0.000 title abstract 5
- 230000000855 fungicidal effect Effects 0.000 title abstract 4
- 230000000694 effects Effects 0.000 title 1
- -1 clozilacon Chemical compound 0.000 abstract 27
- 239000003112 inhibitor Substances 0.000 abstract 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 9
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 5
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 abstract 4
- 230000029058 respiratory gaseous exchange Effects 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 abstract 2
- 239000005766 Dodine Substances 0.000 abstract 2
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 abstract 2
- LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 abstract 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 abstract 2
- 239000005821 Propamocarb Substances 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 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
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 abstract 2
- 239000011575 calcium Substances 0.000 abstract 2
- 229910052791 calcium Inorganic materials 0.000 abstract 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 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 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
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 abstract 2
- JGCSKOVQDXEQHI-UHFFFAOYSA-N phenazine-1-carboxylic acid Chemical compound C1=CC=C2N=C3C(C(=O)O)=CC=CC3=NC2=C1 JGCSKOVQDXEQHI-UHFFFAOYSA-N 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 abstract 2
- QJBZDBLBQWFTPZ-UHFFFAOYSA-N pyrrolnitrin Chemical compound [O-][N+](=O)C1=C(Cl)C=CC=C1C1=CNC=C1Cl QJBZDBLBQWFTPZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000011734 sodium Substances 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 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
- 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
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 abstract 1
- VPWGKZJMAGHQMR-OVVQPSECSA-N (2e)-2-[2-[6-(3-chloro-2-methylphenoxy)-5-fluoropyrimidin-4-yl]oxyphenyl]-2-methoxyimino-n-methylacetamide Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1OC1=NC=NC(OC=2C(=C(Cl)C=CC=2)C)=C1F VPWGKZJMAGHQMR-OVVQPSECSA-N 0.000 abstract 1
- 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 abstract 1
- XDEHMKQLKPZERH-BYPYZUCNSA-N (2s)-2-amino-3-methylbutanamide Chemical compound CC(C)[C@H](N)C(N)=O XDEHMKQLKPZERH-BYPYZUCNSA-N 0.000 abstract 1
- AESOVJYUXGEHCV-UHFFFAOYSA-N (5-bromo-2-methoxy-4-methylpyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(Br)=CN=C1OC AESOVJYUXGEHCV-UHFFFAOYSA-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
- 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
- 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 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
- 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
- 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 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
- OILIYWFQRJOPAI-UHFFFAOYSA-N 2-(2-chlorophenyl)-1h-benzimidazole Chemical compound ClC1=CC=CC=C1C1=NC2=CC=CC=C2N1 OILIYWFQRJOPAI-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
- HZJKXKUJVSEEFU-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile Chemical compound C=1C=C(Cl)C=CC=1C(CCCC)(C#N)CN1C=NC=N1 HZJKXKUJVSEEFU-UHFFFAOYSA-N 0.000 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
- NCDBYAPSWOPDRN-UHFFFAOYSA-N 2-[dichloro(fluoro)methyl]sulfanylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)F)C(=O)C2=C1 NCDBYAPSWOPDRN-UHFFFAOYSA-N 0.000 abstract 1
- PVTHJAPFENJVNC-UHFFFAOYSA-N 2-amino-2-[5-amino-2-methyl-6-(2,3,4,5,6-pentahydroxycyclohexyl)oxyoxan-3-yl]iminoacetic acid Chemical compound NC1CC(N=C(N)C(O)=O)C(C)OC1OC1C(O)C(O)C(O)C(O)C1O PVTHJAPFENJVNC-UHFFFAOYSA-N 0.000 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
- 229940061334 2-phenylphenol Drugs 0.000 abstract 1
- ZVOWUYIDRJPVTD-UHFFFAOYSA-N 3,4,5-trichloropyridine-2,6-dicarbonitrile Chemical compound ClC1=C(Cl)C(C#N)=NC(C#N)=C1Cl ZVOWUYIDRJPVTD-UHFFFAOYSA-N 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
- OVFHHJZHXHZIHT-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)quinazolin-4-one Chemical compound ClC1=CC(Cl)=CC=C1N1C(=O)C2=CC=CC=C2N=C1N1N=CN=C1 OVFHHJZHXHZIHT-UHFFFAOYSA-N 0.000 abstract 1
- BZGLBXYQOMFXAU-UHFFFAOYSA-N 3-(2-methylpiperidin-1-yl)propyl 3,4-dichlorobenzoate Chemical compound CC1CCCCN1CCCOC(=O)C1=CC=C(Cl)C(Cl)=C1 BZGLBXYQOMFXAU-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
- XHTZYMTVLCHVLD-UHFFFAOYSA-N 3-(difluoromethyl)-1-methyl-n-[2-(1,1,2,2-tetrafluoroethoxy)phenyl]pyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1OC(F)(F)C(F)F XHTZYMTVLCHVLD-UHFFFAOYSA-N 0.000 abstract 1
- JZRXHLPCGMDOOT-UHFFFAOYSA-N 3-(difluoromethyl)-n-[4-fluoro-2-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=C(F)C=C1OC(F)(F)C(F)C(F)(F)F JZRXHLPCGMDOOT-UHFFFAOYSA-N 0.000 abstract 1
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-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
- FXSRCEOKVUFSGM-UHFFFAOYSA-N 4-(4-chlorophenyl)-5-(2,6-difluorophenyl)-3,6-dimethylpyridazine Chemical compound C=1C=C(Cl)C=CC=1C=1C(C)=NN=C(C)C=1C1=C(F)C=CC=C1F FXSRCEOKVUFSGM-UHFFFAOYSA-N 0.000 abstract 1
- NNPRCLUGHFXSOU-UHFFFAOYSA-N 4-chloro-n-[cyano(ethoxy)methyl]benzamide Chemical compound CCOC(C#N)NC(=O)C1=CC=C(Cl)C=C1 NNPRCLUGHFXSOU-UHFFFAOYSA-N 0.000 abstract 1
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 abstract 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 abstract 1
- GDGIVSREGUOIJZ-UHFFFAOYSA-N 5-amino-3h-1,3,4-thiadiazole-2-thione Chemical compound NC1=NN=C(S)S1 GDGIVSREGUOIJZ-UHFFFAOYSA-N 0.000 abstract 1
- ASMNSUBMNZQTTG-UHFFFAOYSA-N 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine Chemical compound C1CC(C)CCN1C1=C(C=2C(=CC(F)=CC=2F)F)C(Cl)=NC2=NC=NN12 ASMNSUBMNZQTTG-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
- VKOGJOUVSCKKRM-UHFFFAOYSA-N 5-ethyl-6-octyl-1,7-dihydro-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound NC1C(CCCCCCCC)=C(CC)N=C2NC=NN21 VKOGJOUVSCKKRM-UHFFFAOYSA-N 0.000 abstract 1
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 abstract 1
- QSOQMBDNBYAXTG-UHFFFAOYSA-N 5-methyl-6-octyl-1,7-dihydro-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound NC1C(CCCCCCCC)=C(C)N=C2NC=NN21 QSOQMBDNBYAXTG-UHFFFAOYSA-N 0.000 abstract 1
- 230000002407 ATP formation Effects 0.000 abstract 1
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 abstract 1
- 239000005964 Acibenzolar-S-methyl Substances 0.000 abstract 1
- 239000005727 Amisulbrom Substances 0.000 abstract 1
- 239000005730 Azoxystrobin Substances 0.000 abstract 1
- 239000005734 Benalaxyl Substances 0.000 abstract 1
- 239000005735 Benalaxyl-M Substances 0.000 abstract 1
- 239000005738 Bixafen Substances 0.000 abstract 1
- 239000005740 Boscalid Substances 0.000 abstract 1
- 239000005741 Bromuconazole Substances 0.000 abstract 1
- 239000005742 Bupirimate Substances 0.000 abstract 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- 239000005973 Carvone Substances 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- 239000005747 Chlorothalonil Substances 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 abstract 1
- 239000005750 Copper hydroxide Substances 0.000 abstract 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005751 Copper oxide Substances 0.000 abstract 1
- 239000005752 Copper oxychloride Substances 0.000 abstract 1
- 239000005644 Dazomet Substances 0.000 abstract 1
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005762 Dimoxystrobin Substances 0.000 abstract 1
- 239000005764 Dithianon Substances 0.000 abstract 1
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- SURYGMYUVAMSRO-UHFFFAOYSA-N n'-[5-(difluoromethyl)-2-methyl-4-(3-trimethylsilylpropoxy)phenyl]-n-ethyl-n-methylmethanimidamide Chemical compound CCN(C)C=NC1=CC(C(F)F)=C(OCCC[Si](C)(C)C)C=C1C SURYGMYUVAMSRO-UHFFFAOYSA-N 0.000 abstract 1
- BLCKKNLGFULNRC-UHFFFAOYSA-L n,n-dimethylcarbamodithioate;nickel(2+) Chemical compound [Ni+2].CN(C)C([S-])=S.CN(C)C([S-])=S BLCKKNLGFULNRC-UHFFFAOYSA-L 0.000 abstract 1
- MEWYBGBLQURRNP-UHFFFAOYSA-N n-(3-ethyl-3,5,5-trimethylcyclohexyl)-3-formamido-2-hydroxybenzamide Chemical compound C1C(C)(C)CC(CC)(C)CC1NC(=O)C1=CC=CC(NC=O)=C1O MEWYBGBLQURRNP-UHFFFAOYSA-N 0.000 abstract 1
- GCIZLUZYQSYVSS-UHFFFAOYSA-N n-[(5-bromo-3-chloropyridin-2-yl)methyl]-2,4-dichloropyridine-3-carboxamide Chemical compound ClC1=CC=NC(Cl)=C1C(=O)NCC1=NC=C(Br)C=C1Cl GCIZLUZYQSYVSS-UHFFFAOYSA-N 0.000 abstract 1
- HQUIFHINFGFWLJ-UHFFFAOYSA-N n-[(cyclopropylmethoxyamino)-[6-(difluoromethoxy)-2,3-difluorophenyl]methylidene]-2-phenylacetamide Chemical compound FC(F)OC1=CC=C(F)C(F)=C1C(NOCC1CC1)=NC(=O)CC1=CC=CC=C1 HQUIFHINFGFWLJ-UHFFFAOYSA-N 0.000 abstract 1
- MQJVOGWREDEYCK-UHFFFAOYSA-N n-[1-(5-bromo-3-chloropyridin-2-yl)ethyl]-2-fluoro-4-iodopyridine-3-carboxamide Chemical compound N=1C=C(Br)C=C(Cl)C=1C(C)NC(=O)C1=C(F)N=CC=C1I MQJVOGWREDEYCK-UHFFFAOYSA-N 0.000 abstract 1
- OZGNYLLQHRPOBR-DHZHZOJOSA-N naftifine Chemical compound C=1C=CC2=CC=CC=C2C=1CN(C)C\C=C\C1=CC=CC=C1 OZGNYLLQHRPOBR-DHZHZOJOSA-N 0.000 abstract 1
- 229960004313 naftifine Drugs 0.000 abstract 1
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- 239000004311 natamycin Substances 0.000 abstract 1
- NCXMLFZGDNKEPB-FFPOYIOWSA-N natamycin Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C[C@@H](C)OC(=O)/C=C/[C@H]2O[C@@H]2C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 NCXMLFZGDNKEPB-FFPOYIOWSA-N 0.000 abstract 1
- 235000005152 nicotinamide Nutrition 0.000 abstract 1
- 239000011570 nicotinamide Substances 0.000 abstract 1
- 238000001668 nucleic acid synthesis Methods 0.000 abstract 1
- 235000010292 orthophenyl phenol Nutrition 0.000 abstract 1
- 229960000321 oxolinic acid Drugs 0.000 abstract 1
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 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
- NAYYNDKKHOIIOD-UHFFFAOYSA-N phthalamide Chemical compound NC(=O)C1=CC=CC=C1C(N)=O NAYYNDKKHOIIOD-UHFFFAOYSA-N 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
- 230000004260 plant-type cell wall biogenesis Effects 0.000 abstract 1
- JPFWJDMDPLEUBD-ITJAGOAWSA-N polyoxorim Polymers O[C@@H]1[C@H](O)[C@@H]([C@H](NC(=O)[C@H]([C@H](O)[C@@H](O)COC(N)=O)N)C(O)=O)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-ITJAGOAWSA-N 0.000 abstract 1
- 229920001021 polysulfide Polymers 0.000 abstract 1
- 239000005077 polysulfide Substances 0.000 abstract 1
- 150000008117 polysulfides Polymers 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
- WTFXJFJYEJZMFO-UHFFFAOYSA-N propamidine Chemical compound C1=CC(C(=N)N)=CC=C1OCCCOC1=CC=C(C(N)=N)C=C1 WTFXJFJYEJZMFO-UHFFFAOYSA-N 0.000 abstract 1
- 229960003761 propamidine Drugs 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
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 abstract 1
- FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 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
- VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-UHFFFAOYSA-N 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 229960002132 pyrrolnitrin Drugs 0.000 abstract 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 abstract 1
- MRUMAIRJPMUAPZ-UHFFFAOYSA-N quinolin-8-ol;sulfuric acid Chemical compound OS(O)(=O)=O.C1=CN=C2C(O)=CC=CC2=C1 MRUMAIRJPMUAPZ-UHFFFAOYSA-N 0.000 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
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 230000002195 synergetic effect Effects 0.000 abstract 1
- 238000003786 synthesis reaction Methods 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
- 229960002722 terbinafine Drugs 0.000 abstract 1
- DOMXUEMWDBAQBQ-WEVVVXLNSA-N terbinafine Chemical compound C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 DOMXUEMWDBAQBQ-WEVVVXLNSA-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
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 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 group COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-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
- 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
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
- 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 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
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-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
- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/30—Microbial fungi; Substances produced thereby or obtained therefrom
- A01N63/32—Yeast
-
- 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
- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/30—Microbial fungi; Substances produced thereby or obtained therefrom
-
- 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
- A01N43/64—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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Mycology (AREA)
- Biotechnology (AREA)
- Virology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Se proporcionan composiciones que mejoran el vigor general de la planta y el rendimiento de la cosecha combinando cantidades agrícolamente eficaces de al menos un agente de control biologico bien tolerado por el medio ambiente y al menos un fungicida químico. Además las composiciones presentan actividad insecticidas y fungicida sinérgica. Reivindicacion 1: Una composicion que comprende: a) un cultivo biologicamente puro de Metschnikowia fructicola, y b) al menos un fungicida seleccionado de entre: (F1) Inhibidores de la síntesis de ácidos nucleicos, por ejemplo benalaxilo, benalaxilo-M, bupirimato, clozilacon, dimetirimol, etirimol, furalaxil, himexazol, metalaxil, metalaxil-M, ofurace, oxadixil y ácido oxolínico; (F2) Inhibidores de la mitosis y de la division celular, por ejemplo benomilo, clorfenazol, dietofencarb, etaboxam, fuberidazol, pencicuron, tiofanato, tiofanato-metilo y zoxamida; (F3) Inhibidores de la respiracion, por ejemplo diflumetorim como inhibidor de la respiracion en el CI; bixafen, boscalid, carboxina, fenfuram, flutolanil, fluopiram, furametpir, furmeciclox, isopirazam (componente 9R), isopirazam (componente 9S), mepronil, oxicarboxina, pentiopirad, tifluzamida como inhibidor de la respiracion en el CII; amisulbrom, azoxistrobina, ciazofamid, dimoxistrobina, enestroburina, famoxadon, fenamidona fluoxastrobina, quresoxim-metilo, metominoestrobina, orisastrobina, picoxistrobina, piraclostrobina, piribencarb, trifloxistrobina como inhibidor de la respiracion en el CIII; (F4) Compuestos capaces de actuar como desacoplador, como, por ejemplo, binapacril, dinocap, fluazinam y meptildinocap; (F5) Inhibidores de la produccion de ATP, por ejemplo acetato de fentina, cloruro de fentina, hidroxido de fentina y siltiofam; (F6) Inhibidores de la biosíntesis de aminoácidos y/o proteínas, por ejemplo andoprim, blasticidina-S, kasugamicina, clorhidrato de kasugamicina hidrato, mepanipirim y; (F7) Inhibidores de la transduccion de la senal, por ejemplo fenpiclonil y quinoxifen; (F8) Inhibidores de la síntesis de lípidos y de la membrana, por ejemplo bifenilo, clozolinato, edifenfos, etridiazol, iodocarb, iprobenfos, isoprotiolano, procimidona, propamocarb, clorhidrato de propamocarb, pirazofos, tolclofosmetilo y vinclozolina; (F9) Inhibidores de la biosíntesis de ergosterol, por ejemplo aldimorf, azaconazol, bitertanol, bromuconazol, ciproconazol diclobutrazol, difenoconazol, diniconazol diniconazol-M, dodemorf, acetato de dodemorf. epoxiconazol, etaconazol, fenarimol, fenbuconazol, fenhexamid, fenpropidin, fenpropimorf, fluquinconazol, flurprimidol, flusilazol, flutriafol, furconazol, furconazol-cis, hexaconazol, imibenconazol, ipconazol, metconazol, miclobutanil, naftifina, nuarimol, oxpoconazol, paclobutrazol, pefurazoato, penconazol, piperalin, procloraz, propiconazol, protioconazol, piributicarb, pirifenox, quinconazol, simeconazol, espiroxamina, tebuconazol terbinafina, tetraconazol, triadimefon, triadimenol, tridemorf, triflumizol, triforina, triticonazol, uniconazol, viniconazol y voriconazol; (F10) Inhibidores de la síntesis de la pared celular, por ejemplo bentiavalicarb, dimethomorf, flumorf, iprovalicarb, mandipropamid, polioxinas, polioxorim, protiocarb, validamicina A y valifenal; (F11) Inhibidores de la biosíntesis de melanina, por ejemplo carpropamid, diclocimet, fenoxanil, ftalida, piroquilona y triciclazol; (F12) Compuestos capaces de inducir una defensa en el huésped, como, por ejemplo, acibenzolar-S-metilo, probenazol y tiadinilo, (F13) Compuestos capaces de tener una accion en multiples sitios, como por ejemplo, caldo bordelés, captafol, captan, clorotalonil, naftenato de cobre, oxido de cobre, oxicloruro de cobre, preparaciones de cobre tales como hidroxido de cobre, sulfato de cobre, diclofluanid, ditianon, dodina, base sin dodina, ferbam, fluorofolpet, folpet, guazatina, acetato de guazatina, iminoctadina, albesilato de iminoctadina, triacetato de iminoctadina, mancopper, mancozeb, maneb, metiram, metiram cinc, oxina-cobre, propamidina, propineb, azufre y preparaciones de azufre, incluidos polisulfuro de calcio, tiram, tolifluanida, zineb y ziram; (F14) Otros compuestos como, por ejemplo, 2,3-dibutil-6-clorotieno[2,3-d]pirimidin-4(3H)-ona, (2Z)-3-amino-2-ciano-3-fenilprop-2-enoato de etilo, piflufeno N-[2-(1,3-dimetilbutil)fenil]-5-fluoro-1,3-dimetil-1H-pirazol-4-carb-oxamida, N-{2-[1,1'-bi(ciclopropil)-2-il]fenil}-3-(difluorometil)-1-metil-1H-pirazol-4-carboxamida, 3-(difluorometil)-1-metil-N-(3',4',5'-trifluorobifenil-2-il)-1H-pirazol-4-carboxamida, 3-(difluorometil)-N-[4-fluoro-2-(1,1,2,3,3,3-hexafluoropropoxi)fenil]-1-metil-1H-pirazol-4-carboxamida, (2E)-2-(2-{[6-(3-cloro-2-metilfenoxi)-5-fluoropirimidin-4-il]oxi}fenil)-2-(metoxi-imino)-N-metiletanamida, (2E)-2-{2-[({[(2E,3E)-4-(2,6-diclorofenil)but-3-en-2-iliden]amino}oxi)metil]fenil}-2-(metoxi-imino)-N-metiletanamida, 2-cloro-N-(1,1,3-trimetil-2,3-dihidro-1H-inden-4-iI)piridina-3-carboxamida, N-(3-etil-3,5,5-trimetilciclohexil)-3-(formilamino)-2-hidroxibenzamida, 5-metoxi-2-metil-4-(2-{[({[1E)-1-[3-(trifluorometil)fenil]etiliden}amino)oxi]metil}fenil)-2,4-dihidro-3H-1,2,4-triazol-3-ona, (2E)-2-(metoxiimino)-N-metil-2-(2-{[({(1E)-1-[3-(trifIuorometil)fenil]etiliden}amino)oxi]metil}fenil)etanamida, (2E)-2-(metoxi-imino)-N-metil-2-{2-[(E)-({1-[3-(trifluorometil)fenil]etoxi}imino)metil]fenil}etanamida, (2E)-2-{2-[({[(1E)-1-(3-{[(E)-1-fluoro-2-feniletenil]oxi}fenil)etiliden]amino}oxi)metil]fenil}-2-(metoxi-imino)-N-metiletanamida, 1-(4-clorofenil)-2-(1H-1,2,4-triazol-1-iI)cicloheptanol, 1-(2,2-dimetil-2,3-dihidro-1H-inden-1-iI)-1H-imidazol-5-carboxilato de metilo, N-etil-N-metil-N'-{2-metil-5-(trifluorometil)-4-[3-(trimetilsilil)propoxi]fenil}imidoformamida, N'-{5-(difluorometil)-2-metil-4-[3-(trimetilsilil)propoxi]fenil}-N-etil-N-metilimidoformamida, 1H-imidazol-1-carbotioato de O-{1-[(4-metoxifenoxi)metil]-2,2-dimetilpropilo}, N-[2-(4-{[3-(4-clorofenil)prop-2-in-1-il]oxi}-3-metoxifenil)etil]-N2-(metlsulfonil)valinamida, 5-cloro-7-(4-metilpiperidin-1-il)-6-(2,4,6-trifluorofenil)[1,2,4]triazolo{1,5-a]pirimidina, 5-amino-1,3,4-tiadiazol-2-tiol, propamocarb-fosetilo, 1H-imidazol-1-carboxilato de 1-[(4-metoxifenoxi)metil]2,2-dimetilpropilo, 1-metil-N-[2-(1,1,2,2-tetrafluoroetoxi)fenil]-3-(trifluorometil)-1H-pirazol-4-carboxamida, 2,3,5,6-tetracloro-4-(metilsulfonil)piridina, 2-butoxi-6-iodo-3-propil-4H-cromen-4-ona, 2- fenilfenol y sales, 3-(difluorometil)-1-metil-N-[2-(1,1,2,2-tetrafluoroetoxi)fenil]-1H-pirazol-4-carboxamida, 3,4,5-tricloropiridina-2,6-dicarbonitrilo, 3-[5-(4-clorofenil)-2,3-dimetilisoxazolidin-3-iI]piridina, 3-cloro-5-(4-clorofenil)-4-(2,6-difluorofenil)-6-metilpiridazina, 4-(4-clorofenil)-5-(2,6-difluorofenil)-3,6-dimetilpiridazina, quinolin-8-ol, quinolin-8-ol sulfato (2:1) (sal), 5-metil-6-octil-3,7-dihidro[1,2,4]triazolo[1,5-a]pirimidin-7-amina, 5-etil-6-octil-3,7-dihidro[1,2,4]triazolo[1,5-a]pirimidin-7-amina, bentiazol, betoxazina, capsimicina, carvona, quinometionato, cloroneb, cufraneb, ciflufenamid, cimoxanil, ciprosulfamida, dazomet, debacarb, diclorofeno, diclomezina, dicloran, difenzoquat, difenzoquat metilsulfato, difenilamina, ecomato, ferimzona, flumetover, fluopicolida, fluoroimida, flusulfamida, flutianil, fosetil-aluminio, fosetil-calcio, fosetil-sodio, hexaclorobenceno, irumamicina, isotianilo, metasulfocarb, (2E)-2-{2-[({ciclopropil[4-metoxifenil)imino]metil}tio)metil]fenil}-3-metoxiacrilato de metilo, isotiocianato de metilo, metrafenona, (5-bromo-2-metoxi-4-metilpiridin-3-il)(2,3,4-trimetoxi-6-metilfenil)metanona, mildiomicina, tolnifanida N-(4-clorobencil)-3-[3-metoxi-4-(prop-2-in-1-iloxi)fenil]propanamida, N-[(4-clorofenil)(ciano)metil]-3-[3-metoxi-4-(prop-2-in-1-iloxi)fenil]propanamida, N-[(5-bromo-3-cloropiridin-2-il)metil]-2,4-dicloropiridina-3-carboxamida, N-[1-(5-bromo-3-cloropiridin-2-iI)etil]-2,4-dicloropiridina-3-carboxamida, N-[1-(5-bromo-3-cloropiridin-2-il)etil]-2-fluoro-4-iodopiridina-3-carboxamida, N-{(Z)[(ciclopropilmetoxi)imino][6-(difluorometoxi)-2,3-difluorofenil]metil}-2-fenilacetamida, N-{(E)-[(ciclopropilmetoxi)imino][6-(difluorometoxi)-2 3-difluorofenil]metil}-2-fenilacetamida, natamicina, dimetilditiocarbamato de níquel, nitrotal-isopropilo, octilinona, oxamocarb, oxifentiína, pentaclorofenol y sales, ácido fenazin-1-carboxílico, fenotrina, ácido fosforoso y sus sales. propamocarb fosetilato, propanosina-sodio proquinazid, pirrolnitrina, quintozeno, 5-amino-2-(1-metiletil)-4-(2-metilfenil)-3-oxo-2,3-dihidro-1H-pirazol1-carbotioato de S-prop-2-en-1-ilo, tecloftalam tecnazeno, triazoxido, triclamida, 5-cloro-N'-fenil-N'-prop-2-in-1-iltiofen-2-sulfonohidrazida y zarilamid.
Applications Claiming Priority (1)
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| EP09163602A EP2269454A1 (en) | 2009-06-24 | 2009-06-24 | Combinations of fungicidally active yeast and fungicides |
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| ARP100102190A AR077183A1 (es) | 2009-06-24 | 2010-06-22 | Combinaciones de levaduras con actividad fungicida y fungicidas |
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| EP (4) | EP2269454A1 (es) |
| JP (1) | JP5676591B2 (es) |
| KR (2) | KR20170096227A (es) |
| CN (1) | CN102480965B (es) |
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| BR (1) | BRPI1013498A2 (es) |
| CA (1) | CA2766325C (es) |
| CL (1) | CL2011003270A1 (es) |
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| PL (1) | PL2445348T3 (es) |
| PT (1) | PT2445348E (es) |
| TW (1) | TW201105242A (es) |
| WO (1) | WO2010149369A1 (es) |
| ZA (1) | ZA201109367B (es) |
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| DE10347090A1 (de) | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| EP1606999A1 (de) * | 2004-06-18 | 2005-12-21 | Bayer CropScience AG | Saatgutbehandlungsmittel für Soja |
| DE102004049041A1 (de) | 2004-10-08 | 2006-04-13 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| DE102004049761A1 (de) * | 2004-10-12 | 2006-04-13 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| DE102005023835A1 (de) * | 2005-05-24 | 2006-12-07 | Bayer Cropscience Ag | Fungizide Wirkstoffkombination |
| ATE551899T1 (de) * | 2005-09-09 | 2012-04-15 | Bayer Cropscience Ag | Feststoff-formulierung fungizider mischungen |
| EP2070413A1 (en) | 2007-12-11 | 2009-06-17 | Bayer CropScience AG | Active compound combinations |
| AU2010272872B2 (en) * | 2009-07-16 | 2014-08-28 | Bayer Intellectual Property Gmbh | Synergistic active substance combinations containing phenyl triazoles |
| KR20130057994A (ko) | 2010-04-14 | 2013-06-03 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 디티이노-테트라카복사미드 유도체 및 미생물 또는 이소플라본의 살진균성 배합물 |
| PT2597951T (pt) | 2010-07-26 | 2017-01-19 | Bayer Ip Gmbh | Utilização de inibidores de succinato desidrogenase e inibidores de complexo iii da cadeia respiratória para melhorar a razão entre microrganismos prejudiciais e benéficos |
| NZ587490A (en) * | 2010-08-20 | 2013-03-28 | Greentide Ltd | Anti-Microbial Compounds containing compounds with a sugar substituent |
| EP2460407A1 (de) * | 2010-12-01 | 2012-06-06 | Bayer CropScience AG | Wirkstoffkombinationen umfassend Pyridylethylbenzamide und weitere Wirkstoffe |
| CN102258047B (zh) * | 2011-05-25 | 2013-07-10 | 江苏龙灯化学有限公司 | 杀菌剂组合物 |
| US9241493B2 (en) | 2011-06-14 | 2016-01-26 | Bayer Intellectual Property Gmbh | Use of an enaminocarbonyl compound in combination with a biological control agent |
| HRP20181753T1 (hr) * | 2012-05-30 | 2018-12-28 | Bayer Cropscience Ag | Pripravak koji sadrži biološko kontrolno sredstvo i trifloksistrobin |
| CN104222118B (zh) * | 2012-07-11 | 2015-12-30 | 陕西美邦农药有限公司 | 一种杀菌组合物 |
| CN102907435A (zh) * | 2012-10-27 | 2013-02-06 | 刘善勇 | 一种抑制草坪草生长的复配植物生长调节剂 |
| CN103271044B (zh) * | 2013-06-24 | 2015-02-11 | 杭州宇龙化工有限公司 | 一种含有噻酰菌胺与噻呋酰胺的杀菌组合物 |
| CN103636627B (zh) * | 2013-11-19 | 2015-04-01 | 广西田园生化股份有限公司 | 含噻呋酰胺与吗啉类杀菌剂的超低容量液剂 |
| CN103749493B (zh) * | 2014-02-14 | 2016-01-27 | 南京南农农药科技发展有限公司 | 一种含有井冈霉素a和噻呋酰胺的复配杀菌剂的悬浮剂及其制备方法 |
| CN104012579B (zh) * | 2014-06-23 | 2017-01-04 | 联保作物科技有限公司 | 一种杀菌组合物及其应用 |
| CN104285989B (zh) * | 2014-09-10 | 2017-06-23 | 广东中迅农科股份有限公司 | 一种含有吡唑醚菌酯和丙烷脒的农药组合物 |
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| DE19857963A1 (de) * | 1998-12-16 | 2000-06-21 | Bayer Ag | Agrochemische Formulierungen |
| WO2002072777A2 (en) * | 2001-03-14 | 2002-09-19 | State Of Israel-Ministry Of Agriculture Agricultural Research Organization | A novel antagonistic yeast useful in controlling spoilage of agricultural produce, methods of use thereof and compositions containing same |
| DE10228102A1 (de) * | 2002-06-24 | 2004-01-15 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
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| DE10228104A1 (de) * | 2002-06-24 | 2004-01-15 | Bayer Cropscience Ag | Fungizide Wirkstoffkombination |
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| DE102005035300A1 (de) * | 2005-07-28 | 2007-02-01 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| ATE551899T1 (de) * | 2005-09-09 | 2012-04-15 | Bayer Cropscience Ag | Feststoff-formulierung fungizider mischungen |
| EP1982717A1 (de) * | 2007-04-20 | 2008-10-22 | Bayer CropScience AG | Verwendung von Fungiziden zur Behandlung von Fischmykosen |
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| CL2008003422A1 (es) * | 2007-11-29 | 2009-08-07 | Bayer Cropscience Ag | Procedimiento para reducir la contaminacion por aflatoxinas y ocratoxinas que afecten a plantas de cereales, frutos secos, frutas y/o especias y/o material vegetal, mediante el uso de uno o mas compuestos fungicidas seleccionado entre 29 compuestos fungicidas distintos. |
| EP2070414A1 (en) * | 2007-12-11 | 2009-06-17 | Bayer CropScience AG | Active compound combinations |
| EP2105049A1 (en) * | 2008-03-28 | 2009-09-30 | Bayer CropScience AG | Method of plant growth promotion using amide compounds |
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2009
- 2009-06-24 EP EP09163602A patent/EP2269454A1/en not_active Withdrawn
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2010
- 2010-06-22 EP EP17185713.9A patent/EP3266305B1/en active Active
- 2010-06-22 AR ARP100102190A patent/AR077183A1/es unknown
- 2010-06-22 PT PT107276875T patent/PT2445348E/pt unknown
- 2010-06-22 EP EP10727687.5A patent/EP2445348B1/en active Active
- 2010-06-22 KR KR1020177022540A patent/KR20170096227A/ko not_active Ceased
- 2010-06-22 KR KR1020117030874A patent/KR101769537B1/ko active Active
- 2010-06-22 WO PCT/EP2010/003817 patent/WO2010149369A1/en not_active Ceased
- 2010-06-22 AU AU2010265093A patent/AU2010265093A1/en not_active Abandoned
- 2010-06-22 EA EA201290010A patent/EA201290010A1/ru unknown
- 2010-06-22 BR BRPI1013498-0A patent/BRPI1013498A2/pt not_active Application Discontinuation
- 2010-06-22 CN CN201080028040.7A patent/CN102480965B/zh active Active
- 2010-06-22 EP EP13197397.6A patent/EP2737797A1/en not_active Withdrawn
- 2010-06-22 PL PL10727687T patent/PL2445348T3/pl unknown
- 2010-06-22 ES ES10727687.5T patent/ES2519168T3/es active Active
- 2010-06-22 JP JP2012516576A patent/JP5676591B2/ja active Active
- 2010-06-22 MX MX2011013933A patent/MX2011013933A/es active IP Right Grant
- 2010-06-22 CA CA2766325A patent/CA2766325C/en active Active
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- 2010-06-23 TW TW099120350A patent/TW201105242A/zh unknown
- 2010-06-24 US US12/822,261 patent/US20110033433A1/en not_active Abandoned
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- 2011-12-20 ZA ZA2011/09367A patent/ZA201109367B/en unknown
- 2011-12-21 CR CR20110700A patent/CR20110700A/es unknown
- 2011-12-22 CL CL2011003270A patent/CL2011003270A1/es unknown
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2014
- 2014-03-26 US US14/225,843 patent/US20140205580A1/en not_active Abandoned
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| EP2269454A1 (en) | 2011-01-05 |
| EP2445348B1 (en) | 2014-08-20 |
| ZA201109367B (en) | 2013-02-27 |
| BRPI1013498A2 (pt) | 2015-08-25 |
| JP2012530742A (ja) | 2012-12-06 |
| EP2737797A1 (en) | 2014-06-04 |
| JP5676591B2 (ja) | 2015-02-25 |
| CA2766325A1 (en) | 2010-12-29 |
| AU2015213382A1 (en) | 2015-09-03 |
| CR20110700A (es) | 2012-05-10 |
| WO2010149369A1 (en) | 2010-12-29 |
| KR20170096227A (ko) | 2017-08-23 |
| PT2445348E (pt) | 2014-10-29 |
| PL2445348T3 (pl) | 2015-01-30 |
| EP3266305B1 (en) | 2020-01-29 |
| TW201105242A (en) | 2011-02-16 |
| CA2766325C (en) | 2018-07-31 |
| AU2010265093A1 (en) | 2012-01-19 |
| US20140205580A1 (en) | 2014-07-24 |
| EA201290010A1 (ru) | 2012-07-30 |
| CL2011003270A1 (es) | 2012-07-13 |
| EP2445348A1 (en) | 2012-05-02 |
| AU2015213382B2 (en) | 2017-03-02 |
| ES2784427T3 (es) | 2020-09-25 |
| MX2011013933A (es) | 2012-04-30 |
| ES2519168T3 (es) | 2014-11-06 |
| CN102480965A (zh) | 2012-05-30 |
| EP3266305A1 (en) | 2018-01-10 |
| US20110033433A1 (en) | 2011-02-10 |
| KR20120040158A (ko) | 2012-04-26 |
| KR101769537B1 (ko) | 2017-08-18 |
| CN102480965B (zh) | 2014-07-16 |
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