AR076150A1 - Uso de sintetico y biologico fungicidas en combinacion para controlar hongos daninos - Google Patents
Uso de sintetico y biologico fungicidas en combinacion para controlar hongos daninosInfo
- Publication number
- AR076150A1 AR076150A1 ARP100100955A ARP100100955A AR076150A1 AR 076150 A1 AR076150 A1 AR 076150A1 AR P100100955 A ARP100100955 A AR P100100955A AR P100100955 A ARP100100955 A AR P100100955A AR 076150 A1 AR076150 A1 AR 076150A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- phenyl
- chloro
- dimethyl
- amino
- Prior art date
Links
- 239000000417 fungicide Substances 0.000 title abstract 4
- -1 miclobutanyl Chemical compound 0.000 abstract 23
- 241001646398 Pseudomonas chlororaphis Species 0.000 abstract 4
- 238000000034 method Methods 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- 241000196324 Embryophyta Species 0.000 abstract 3
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 241000233866 Fungi Species 0.000 abstract 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 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
- 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
- 150000002148 esters Chemical class 0.000 abstract 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N ethyl acetate Substances CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 2
- 230000000855 fungicidal effect Effects 0.000 abstract 2
- 239000002207 metabolite Substances 0.000 abstract 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 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 2
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 abstract 1
- JQEUPNKUYMHYPW-LLVKDONJSA-N (1r)-n-methyl-1,2,3,4-tetrahydronaphthalen-1-amine Chemical compound C1=CC=C2[C@H](NC)CCCC2=C1 JQEUPNKUYMHYPW-LLVKDONJSA-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
- 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
- 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
- RWXHELMQMYFBOP-UHFFFAOYSA-N 1-[1-(4-cyanophenyl)ethylsulfonyl]butan-2-ylcarbamic acid Chemical compound OC(=O)NC(CC)CS(=O)(=O)C(C)C1=CC=C(C#N)C=C1 RWXHELMQMYFBOP-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
- 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
- VPWGKZJMAGHQMR-UHFFFAOYSA-N 2-[2-[6-(3-chloro-2-methylphenoxy)-5-fluoropyrimidin-4-yl]oxyphenyl]-2-methoxyimino-n-methylacetamide Chemical compound CNC(=O)C(=NOC)C1=CC=CC=C1OC1=NC=NC(OC=2C(=C(Cl)C=CC=2)C)=C1F VPWGKZJMAGHQMR-UHFFFAOYSA-N 0.000 abstract 1
- CACOMUHPQMDEJQ-UHFFFAOYSA-N 2-amino-4-methyl-n-phenyl-1,3-thiazole-5-carboxamide Chemical compound N1=C(N)SC(C(=O)NC=2C=CC=CC=2)=C1C CACOMUHPQMDEJQ-UHFFFAOYSA-N 0.000 abstract 1
- ZRDUSMYWDRPZRM-UHFFFAOYSA-N 2-sec-butyl-4,6-dinitrophenyl 3-methylbut-2-enoate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)C=C(C)C ZRDUSMYWDRPZRM-UHFFFAOYSA-N 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
- 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
- HXKPOEOLTWELSY-UHFFFAOYSA-N 3-(difluoromethyl)-1-methyl-n-[2-[4-(trifluoromethylsulfanyl)phenyl]phenyl]pyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC=C(SC(F)(F)F)C=C1 HXKPOEOLTWELSY-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
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 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
- BOSKZYFDVJDHMQ-UHFFFAOYSA-N 5-amino-4-(2-methylphenyl)-3-oxo-2-propan-2-ylpyrazole-1-carbothioic s-acid Chemical compound O=C1N(C(C)C)N(C(O)=S)C(N)=C1C1=CC=CC=C1C BOSKZYFDVJDHMQ-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
- 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
- GOFJDXZZHFNFLV-UHFFFAOYSA-N 5-fluoro-1,3-dimethyl-N-[2-(4-methylpentan-2-yl)phenyl]pyrazole-4-carboxamide Chemical compound CC(C)CC(C)C1=CC=CC=C1NC(=O)C1=C(F)N(C)N=C1C GOFJDXZZHFNFLV-UHFFFAOYSA-N 0.000 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
- 239000005964 Acibenzolar-S-methyl Substances 0.000 abstract 1
- 239000005730 Azoxystrobin Substances 0.000 abstract 1
- 244000063299 Bacillus subtilis Species 0.000 abstract 1
- 235000014469 Bacillus subtilis Nutrition 0.000 abstract 1
- 241000894006 Bacteria Species 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
- 239000005739 Bordeaux mixture Substances 0.000 abstract 1
- 239000005741 Bromuconazole Substances 0.000 abstract 1
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 abstract 1
- 239000005742 Bupirimate Substances 0.000 abstract 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 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
- 239000005752 Copper oxychloride Substances 0.000 abstract 1
- 239000005756 Cymoxanil 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
- HDWLUGYOLUHEMN-UHFFFAOYSA-N Dinobuton Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)OC(C)C HDWLUGYOLUHEMN-UHFFFAOYSA-N 0.000 abstract 1
- 239000005766 Dodine Substances 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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- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 abstract 1
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- YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical compound [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 abstract 1
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- MKIMSXGUTQTKJU-UHFFFAOYSA-N Propamocarb hydrochloride Chemical compound [Cl-].CCCOC(=O)NCCC[NH+](C)C MKIMSXGUTQTKJU-UHFFFAOYSA-N 0.000 abstract 1
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- 235000010296 thiabendazole Nutrition 0.000 abstract 1
- 229960004546 thiabendazole Drugs 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
- 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
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
-
- 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
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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
-
- 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
- A01N63/20—Bacteria; Substances produced thereby or obtained therefrom
- A01N63/22—Bacillus
-
- 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
- A01N65/00—Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N65/00—Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
- A01N65/08—Magnoliopsida [dicotyledons]
- A01N65/30—Polygonaceae [Buckwheat family], e.g. red-knees or rhubarb
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Mycology (AREA)
- Virology (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Abstract
Uso combinado de fungicidas sintéticos y agentes de control biologico para controlar hongos daninos. Para ser más precisos, un método para controlar hongos daninos, el cual comprende al menos dos bloques de tratamiento, en donde en al menos un bloque de tratamiento las plantas son tratadas con al menos un fungicida sintético y en al menos un bloque de tratamiento las plantas son tratadas con al menos un agente de control biologico, con la condicion de que el ultimo bloque de tratamiento comprende someter las plantas al menos a un tratamiento con al menos un agente de control biologico. Reivindicacion 8: El método de acuerdo con cualquiera de las reivindicaciones precedentes, caracterizado porque el agente de control biologico se selecciona de bacterias no patogenas, metabolitos producidos por ellas; hongos no patogenos, metabolitos producidos por ellos; ácidos de resina y extractos vegetales, especialmente de Reynoutria sachalinensis. Reivindicacion 9: El método de acuerdo con la reivindicacion 8, caracterizado porque la bacteria saprofita es Bacillus subtilis. Reivindicacion 11: El método de acuerdo con cualquiera de las reivindicaciones precedentes, caracterizado porque el fungicida sintético se selecciona de A) azoles, seleccionados del grupo que consiste en 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, triadimefon, triadimenol, triticonazol, uniconazol, 1-(4-cloro-fenil)-2-([1,2,4]triazol-1-il)-cicloheptanol, ciazofamida, imazalilo, pefurazoato, procloraz, triflumizol, benomilo, carbendazim, fuberidazol, tiabendazol, etaboxam, etridiazol, himexazol y 2-(4-cloro-fenil)-N-[4-(3,4-dimetoxi-fenil)-isoxazol-5-il]-2-prop-2-iniloxi-acetamida; B) estrobilurinas, seleccionadas del grupo que consiste en azoxistrobina, dimoxistrobina, enestroburina, fluoxastrobina, cresoxim-metilo, metominostrobina, orisastrobina, picoxistrobina, piraclostrobina, piribencarb, trifloxistrobina, 2-(2-(6-(3-cloro-2-metil-fenoxi)-5-fluoro-pirimidin-4-iloxi)-fenil)-2-metoxiimino-N-metil-acetamida, éster metílico del ácido 3-metoxi-2-(2-(N-(4-metoxi-fenil)-ciclopropan-carboximidoil-sulfanilmetil)-fenil)-acrílico, (2-cloro-5-[1-(3-metilbenciloxiimino)-etil]bencil)carbamato de metilo y 2-(2-(3-(2,6-diclorofenil)-1-metil-allilideneaminooximetil)-fenil)-2-metoxiimino-N-metil-acetamida; C) carboxamidas, seleccionadas del grupo que consiste en benalaxilo, benalaxil-M, benodanilo, bixafeno, boscalida, carboxina, fenfuram, fenhexamida, flutolanilo, furametpir, isopirazam, isotianilo, kiralaxilo, mepronilo, metalaxilo, metalaxilo-M (mefenoxam), ofurace, oxadixilo, oxicarboxina, pentiopirad, sedaxano, tecloftalam, tifluzamida, tiadinilo, 2-amino-4-metil-tiazol-5-carboxanilida, 2-cloro-N-(1,3-trimetil-indan-4-il)-nicotinamida, N-(3',4',5'-trifluorobifenil-2-il)-3-difluorometil-1-metil-1H-pirazol-4-carboxamida, N-(4'-trifluorometiltiobifenil-2-il)-3-difluorometil-1-metil-1H-pirazol-4-carboxamida, N-(2-(1,3-dimetil-butil)-fenil)-1,3-dimetil-5-fluoro-1H-pirazol-4-carboxamida y N-(2-(1,3,3-trimetil-butil)-fenil)-1,3-dimetil-5-fluoro-1H-pirazol-4- carboxamida, dimetomorf, flumorf, pirimorf, flumetover, fluopicolida, fluopiram, zoxamida, N-(3-Etil-3,5,5-trimetil-ciclohexil)-3-formiIamino-2-hidroxi-benzamida, carpropamida, diciclomet, mandiproamida, oxitetraciclina, siltiofarm y amida del ácido N-(6-metoxi-piridin-3-il)-ciclopropancarboxílico, D) compuestos heterocíclicos seleccionados del grupo que consiste en fluazinam, pirifenox, 3-[5-(4-cloro-fenil)-2,3-dimetil-isoxazolidin-3-iI]-piridina, 3-[5-(4-metil-fenil)-2,3-dimetil-isoxazolidin-3-il]-piridina, 2,3,5,6-tetra-cloro-4-metansulfonil-piridina, 3,4,5-tricloropiridin-2,6-di-carbonitrilo, N-(1-(5-bromo-3-cloro-piridin-2-il)-etil)-2,4-dicloro-nicotinamida, N-[(5-bromo-3-cloro-piridin-2-il)-metil]-2,4-dicloro-nicotinamida, bupirimate, ciprodinilo, diflumetorim, fenarimol, ferimzona, mepanipirim, nitrapirina, nuarimol, pirimetanilo, triforina, fenpiclonilo, fludioxonilo, aldimorf, dodemorf, acetato de dodemorf, fenpropimorf, tridemorf, fenpropidina, fluoroimida, iprodiona, procimidona, vinclozolina, famoxadona, fenamidona, flutianilo, octilinona, probenazol, éster S-alílico del ácido 5-amino-2-isopropil-3-oxo-4-orto-tolil-2,3-dihidro-pirazol-1-carbotioico, acibenzolar-S-metilo, amisulbromo, anilazina, blasticidina-S, captafol, captano, quinometionato, dazomet, debacarb, diclomezina, difenzoquat, metilsulfato de difenzoquat, fenoxanilo, folpet, ácido oxolínico, piperalina, proquinazida, piroquilona, quinoxifeno, triazoxida, triciclazol, 2- butoxi-6-yodo-3-propilcromen-4-ona, 5-cloro-1-(4,6-dimetoxi-pirimidin-2-il)-2-metil-1H-benzoimidazol, 5-cloro-7-(4-metilpiperidin-1-il)-6-(2,4,6-trifluorofenil)-[1,2,4]triazolo[1,5-a]pirimidina y 5-etil-6-octil-[1,2,4]triazolo[1,5-a]pirimidin-7-ilamina; E) carbamatos, seleccionados del grupo que consiste en ferbam, mancozeb, maneb, metam, metasulfocarb, metiram, propineb, tiram, zineb, ziram, bentiavalicarb, dietofencarb, iprovalicarb, propamocarb, clorhidrato de propamocarb, valifenal y éster (4-fluorofenílico) del ácido N-(1-(1-(4-ciano-fenil)etanesulfonil)-but-2-il) carbámico; y F) otros compuestos activos, seleccionados del grupo que consiste en guanidinas: guanidina, dodina, base libre de dodina, guazatina, acetato de guazatina, iminoctadina, triacetato de iminoctadina, tris(albesilato) de iminoctadina; derivados de nitrofenilo: binapacrilo, dinobuton, dinocap, nitrtal-isopropilo, tecnazeno, compuestos organometálicos: sales de fentina, tales como acetato de fentina, cloruro de fentina o hidroxido de fentina; compuestos heterociclilo que contienen azufre: ditianona, isoprotiolano; compuestos de organofosforo: edifenfos, fosetilo, fosetil-aluminio, iprobenfos, ácido fosforoso y sus sales, pirazofos, tolclofos-metilo; compuestos de organocloro: clorotalonilo, diclofluanida, diclorofeno, flusulfamida, hexaclorobenceno, pencicurona, pentaclorfenol y sus sales, ftalida, quintoceno, tiofanato-metilo, tolilfluanida, N-(4-cloro-2-nitro-fenil)-N-etil-4-metil-bencensulfonamida; sustancias activas inorgánicas: mezcla de Bordeaux, acetato de cobre, hidroxido de cobre, oxicloruro de cobre, sulfato de cobre básico, azufre; otros: bifenilo, bronopol, ciflufenamida, cimoxanilo, difenilamina, metrafenona, mildiomicina, oxina-cobre, prohexadiona-calcio, espiroxamina, tolilfluanida, 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)-2,5-dimetil-fenil)-N-etil-N-metilformamidina, N'-(2-metil-5-trifluorometil-4-(3-trimetilsilanil-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}-tiazol-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}-tiazol-4-carboxílico, éster 6-ter-butil-8-fluoro-2,3-dimetil-quinolin-4-ílico de ácido acético y éster 6-ter-butil-8-fluoro-2,3-dimetil-quinoIin-4-ílico de ácido metoxi-acético; y sus mezclas.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09156360 | 2009-03-26 | ||
| EP09169871 | 2009-09-09 |
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|---|---|
| AR076150A1 true AR076150A1 (es) | 2011-05-18 |
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| Application Number | Title | Priority Date | Filing Date |
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| ARP100100955A AR076150A1 (es) | 2009-03-26 | 2010-03-25 | Uso de sintetico y biologico fungicidas en combinacion para controlar hongos daninos |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US20120003199A1 (es) |
| EP (1) | EP2410840A2 (es) |
| JP (1) | JP5920983B2 (es) |
| KR (1) | KR101737138B1 (es) |
| CN (2) | CN102361551B (es) |
| AR (1) | AR076150A1 (es) |
| AU (2) | AU2010227493A1 (es) |
| BR (1) | BRPI1006415B1 (es) |
| CA (1) | CA2753150C (es) |
| CL (1) | CL2011002376A1 (es) |
| CR (1) | CR20110460A (es) |
| EA (1) | EA019044B1 (es) |
| EC (1) | ECSP11011349A (es) |
| IL (1) | IL214765A0 (es) |
| MX (2) | MX2011009295A (es) |
| NZ (1) | NZ594887A (es) |
| PE (1) | PE20120536A1 (es) |
| WO (1) | WO2010108973A2 (es) |
| ZA (1) | ZA201107754B (es) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20150066600A (ko) | 2007-09-20 | 2015-06-16 | 바스프 에스이 | 살진균성 균주 및 활성 화합물을 포함하는 조합물 |
| AR077432A1 (es) * | 2009-07-30 | 2011-08-24 | Marrone Bio Innovations | Combinaciones de inhibidor de patogenos de planta y metodos de uso |
| EP2460407A1 (de) | 2010-12-01 | 2012-06-06 | Bayer CropScience AG | Wirkstoffkombinationen umfassend Pyridylethylbenzamide und weitere Wirkstoffe |
| EP2462807A1 (en) * | 2010-12-08 | 2012-06-13 | Basf Se | Pesticidal mixtures comprising pyraclostrobin |
| ES2864092T3 (es) | 2011-01-28 | 2021-10-13 | Deepak Pranjivandas Shah | Composición plaguicida que comprende azufre, un fungicida y un excipiente agroquímico |
| CN102172239A (zh) * | 2011-03-25 | 2011-09-07 | 陕西先农生物科技有限公司 | 粉唑醇·戊唑醇杀菌组合物 |
| KR20140053026A (ko) | 2011-05-24 | 2014-05-07 | 바이엘 크롭사이언스 엘피 | 폴리엔 살진균제와 비-리보솜 펩티드의 상승작용적 조합물 및 관련된 사용 방법 |
| BR112014018511A8 (pt) * | 2012-01-27 | 2017-07-11 | Gfs Corp Aus Pty Ltd | Método de produção de biotensoativos |
| JP5916098B2 (ja) * | 2012-02-27 | 2016-05-11 | 関西電力株式会社 | 植物病害防除資材及び植物病害防除方法 |
| CN109169661B (zh) | 2012-05-30 | 2021-09-21 | 拜耳作物科学股份公司 | 包括生物防治剂和杀昆虫剂的组合物 |
| ES2703754T3 (es) * | 2012-05-30 | 2019-03-12 | Bayer Cropscience Ag | Composición que comprende un agente de control biológico y un fungicida seleccionado de metalaxilo y metalaxil-M |
| ES2737754T3 (es) * | 2012-05-30 | 2020-01-15 | Bayer Cropscience Ag | Composición que comprende un agente de control biológico y un fungicida seleccionado de inhibidores de la biosíntesis de aminoácidos o proteínas, inhibidores de producción de ATP e inhibidores de la síntesis de la pared celular |
| AU2013269660B2 (en) | 2012-05-30 | 2016-07-07 | Bayer Cropscience Ag | Compositiions comprising a biological control agent and an insecticide |
| NZ725994A (en) * | 2012-05-30 | 2018-07-27 | Bayer Cropscience Ag | Composition comprising a biological control agent and a fungicide selected from inhibitors of the ergosterol biosynthesis |
| WO2013178651A1 (en) * | 2012-05-30 | 2013-12-05 | Bayer Cropscience Ag | Composition comprising a biological control agent and a fungicide selected from inhibitors of the mitosis and cell division or compounds having a multi-site action |
| US9386773B2 (en) * | 2012-05-30 | 2016-07-12 | Bayer Cropscience Ag | Compositions comprising a biological control agent and a fungicide from the group consisting of inhibitors of the respiratory chain at complex I or II |
| CN107996613B (zh) * | 2012-05-30 | 2021-10-22 | 拜尔农作物科学股份公司 | 包括生物防治剂和杀虫剂的组合物 |
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| KR20150066600A (ko) * | 2007-09-20 | 2015-06-16 | 바스프 에스이 | 살진균성 균주 및 활성 화합물을 포함하는 조합물 |
-
2010
- 2010-03-25 BR BRPI1006415-0A patent/BRPI1006415B1/pt active IP Right Grant
- 2010-03-25 PE PE2011001716A patent/PE20120536A1/es not_active Application Discontinuation
- 2010-03-25 CA CA2753150A patent/CA2753150C/en active Active
- 2010-03-25 CN CN201080012614.1A patent/CN102361551B/zh active Active
- 2010-03-25 EA EA201101333A patent/EA019044B1/ru not_active IP Right Cessation
- 2010-03-25 NZ NZ594887A patent/NZ594887A/xx unknown
- 2010-03-25 MX MX2011009295A patent/MX2011009295A/es active IP Right Grant
- 2010-03-25 CN CN201510039303.9A patent/CN104719344B/zh active Active
- 2010-03-25 WO PCT/EP2010/053867 patent/WO2010108973A2/en not_active Ceased
- 2010-03-25 US US13/259,541 patent/US20120003199A1/en not_active Abandoned
- 2010-03-25 EP EP10710047A patent/EP2410840A2/en not_active Ceased
- 2010-03-25 MX MX2014005780A patent/MX349773B/es unknown
- 2010-03-25 AR ARP100100955A patent/AR076150A1/es active IP Right Grant
- 2010-03-25 JP JP2012501304A patent/JP5920983B2/ja active Active
- 2010-03-25 KR KR1020117025154A patent/KR101737138B1/ko active Active
- 2010-03-25 AU AU2010227493A patent/AU2010227493A1/en not_active Abandoned
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2011
- 2011-08-21 IL IL214765A patent/IL214765A0/en unknown
- 2011-08-25 CR CR20110460A patent/CR20110460A/es unknown
- 2011-09-23 EC EC2011011349A patent/ECSP11011349A/es unknown
- 2011-09-26 CL CL2011002376A patent/CL2011002376A1/es unknown
- 2011-10-24 ZA ZA2011/07754A patent/ZA201107754B/en unknown
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2014
- 2014-04-01 US US14/242,133 patent/US20140212401A1/en not_active Abandoned
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2016
- 2016-03-29 AU AU2016201930A patent/AU2016201930A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20120003199A1 (en) | 2012-01-05 |
| WO2010108973A3 (en) | 2011-04-21 |
| CR20110460A (es) | 2011-10-24 |
| BRPI1006415A2 (pt) | 2015-08-25 |
| CN102361551B (zh) | 2015-09-16 |
| MX2011009295A (es) | 2011-09-27 |
| US20140212401A1 (en) | 2014-07-31 |
| AU2010227493A1 (en) | 2011-10-20 |
| ZA201107754B (en) | 2014-12-23 |
| JP5920983B2 (ja) | 2016-05-24 |
| KR20110132461A (ko) | 2011-12-07 |
| CA2753150A1 (en) | 2010-09-30 |
| CA2753150C (en) | 2017-04-18 |
| ECSP11011349A (es) | 2011-10-31 |
| CN102361551A (zh) | 2012-02-22 |
| CN104719344A (zh) | 2015-06-24 |
| NZ594887A (en) | 2013-11-29 |
| WO2010108973A2 (en) | 2010-09-30 |
| JP2012521390A (ja) | 2012-09-13 |
| EP2410840A2 (en) | 2012-02-01 |
| IL214765A0 (en) | 2011-11-30 |
| EA019044B1 (ru) | 2013-12-30 |
| MX349773B (es) | 2017-08-10 |
| PE20120536A1 (es) | 2012-05-05 |
| AU2016201930A1 (en) | 2016-04-21 |
| EA201101333A1 (ru) | 2012-05-30 |
| CL2011002376A1 (es) | 2012-02-17 |
| KR101737138B1 (ko) | 2017-05-17 |
| CN104719344B (zh) | 2018-11-13 |
| BRPI1006415B1 (pt) | 2018-01-23 |
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