ES2737754T3 - 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 - Google Patents
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 Download PDFInfo
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- ES2737754T3 ES2737754T3 ES13726742T ES13726742T ES2737754T3 ES 2737754 T3 ES2737754 T3 ES 2737754T3 ES 13726742 T ES13726742 T ES 13726742T ES 13726742 T ES13726742 T ES 13726742T ES 2737754 T3 ES2737754 T3 ES 2737754T3
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- methyl
- spp
- carboxamide
- fungicide
- plants
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- 239000000203 mixture Substances 0.000 title claims abstract description 141
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 137
- 239000000417 fungicide Substances 0.000 title claims abstract description 137
- 241001646398 Pseudomonas chlororaphis Species 0.000 title claims abstract description 86
- 239000003112 inhibitor Substances 0.000 title claims description 35
- 150000001413 amino acids Chemical class 0.000 title claims description 8
- 230000002407 ATP formation Effects 0.000 title claims description 5
- 230000014616 translation Effects 0.000 title claims description 4
- 230000004260 plant-type cell wall biogenesis Effects 0.000 title description 4
- 244000063299 Bacillus subtilis Species 0.000 claims abstract description 21
- 235000014469 Bacillus subtilis Nutrition 0.000 claims abstract description 21
- 230000002195 synergetic effect Effects 0.000 claims abstract description 16
- 239000005797 Iprovalicarb Substances 0.000 claims abstract description 6
- 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 claims abstract description 6
- 241000238631 Hexapoda Species 0.000 claims description 82
- -1 bentiazole Chemical class 0.000 claims description 46
- 150000001875 compounds Chemical class 0.000 claims description 41
- 238000000034 method Methods 0.000 claims description 37
- 239000000126 substance Substances 0.000 claims description 35
- 230000003032 phytopathogenic effect Effects 0.000 claims description 32
- 239000003795 chemical substances by application Substances 0.000 claims description 30
- 241000244206 Nematoda Species 0.000 claims description 29
- 241000238876 Acari Species 0.000 claims description 24
- 235000013399 edible fruits Nutrition 0.000 claims description 23
- 125000006269 biphenyl-2-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C(*)C([H])=C([H])C([H])=C1[H] 0.000 claims description 21
- 150000003839 salts Chemical class 0.000 claims description 18
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- 239000002270 dispersing agent Substances 0.000 claims description 13
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- 239000002917 insecticide Substances 0.000 claims description 12
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- 230000006378 damage Effects 0.000 claims description 10
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims description 8
- 239000002671 adjuvant Substances 0.000 claims description 8
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- 239000003981 vehicle Substances 0.000 claims description 8
- 230000015572 biosynthetic process Effects 0.000 claims description 7
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 7
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 239000002562 thickening agent Substances 0.000 claims description 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 7
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- 230000009471 action Effects 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 claims description 5
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- 230000007123 defense Effects 0.000 claims description 5
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims description 5
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 claims description 5
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- 238000003786 synthesis reaction Methods 0.000 claims description 4
- 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 claims description 3
- 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 claims description 3
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 3
- 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 claims description 3
- XFOXDUJCOHBXRC-UHFFFAOYSA-N N-Ethyl-N-methyl-4-(trifluoromethyl)-2-(3,4-dimethoxyphenyl)benzamide Chemical compound CCN(C)C(=O)C1=CC=C(C(F)(F)F)C=C1C1=CC=C(OC)C(OC)=C1 XFOXDUJCOHBXRC-UHFFFAOYSA-N 0.000 claims description 3
- 239000005821 Propamocarb Substances 0.000 claims description 3
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- UWQMKVBQKFHLCE-UHFFFAOYSA-N diclomezine Chemical compound C1=C(Cl)C(C)=C(Cl)C=C1C1=NNC(=O)C=C1 UWQMKVBQKFHLCE-UHFFFAOYSA-N 0.000 claims description 3
- IPENDKRRWFURRE-UHFFFAOYSA-N fluoroimide Chemical compound C1=CC(F)=CC=C1N1C(=O)C(Cl)=C(Cl)C1=O IPENDKRRWFURRE-UHFFFAOYSA-N 0.000 claims description 3
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 claims description 3
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 3
- AMSPWOYQQAWRRM-UHFFFAOYSA-N metrafenone Chemical compound COC1=CC=C(Br)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC AMSPWOYQQAWRRM-UHFFFAOYSA-N 0.000 claims description 3
- 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 claims description 3
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- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 claims description 3
- 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 claims description 2
- XDEHMKQLKPZERH-BYPYZUCNSA-N (2s)-2-amino-3-methylbutanamide Chemical compound CC(C)[C@H](N)C(N)=O XDEHMKQLKPZERH-BYPYZUCNSA-N 0.000 claims description 2
- 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 claims description 2
- QEUOHPLVFSQWME-CYVLTUHYSA-N (z)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-morpholin-4-ylprop-2-en-1-one Chemical compound C1=CC(C(C)(C)C)=CC=C1C(\C=1C=C(Cl)N=CC=1)=C\C(=O)N1CCOCC1 QEUOHPLVFSQWME-CYVLTUHYSA-N 0.000 claims description 2
- DUWKZHIPEWZXNC-UHFFFAOYSA-N 1-methyl-3-(trifluoromethyl)-n-[2-[2-(trifluoromethyl)phenyl]phenyl]pyrazole-4-carboxamide Chemical compound FC(F)(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC=CC=C1C(F)(F)F DUWKZHIPEWZXNC-UHFFFAOYSA-N 0.000 claims description 2
- OKRROXQXGNEUSS-UHFFFAOYSA-N 1h-imidazol-1-ium-1-carboxylate Chemical compound OC(=O)N1C=CN=C1 OKRROXQXGNEUSS-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- MQFJRLQNQOJQEI-HXUWFJFHSA-N 2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]-1-[4-[4-[(5r)-5-phenyl-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl]piperidin-1-yl]ethanone Chemical compound CC1=CC(C(F)(F)F)=NN1CC(=O)N1CCC(C=2SC=C(N=2)C=2C[C@@H](ON=2)C=2C=CC=CC=2)CC1 MQFJRLQNQOJQEI-HXUWFJFHSA-N 0.000 claims description 2
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- 229940061334 2-phenylphenol Drugs 0.000 claims description 2
- 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 claims description 2
- TUGLVMDNIRDNER-UHFFFAOYSA-N 3-(difluoromethyl)-1-methyl-n-[2-[4-(trifluoromethyl)phenyl]phenyl]pyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC=C(C(F)(F)F)C=C1 TUGLVMDNIRDNER-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
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- ZALZMUXMSIVXKA-UHFFFAOYSA-N 5-fluoro-2-[(4-fluorophenyl)methoxy]pyrimidin-4-amine Chemical compound C1=C(F)C(N)=NC(OCC=2C=CC(F)=CC=2)=N1 ZALZMUXMSIVXKA-UHFFFAOYSA-N 0.000 claims description 2
- CGRCPZUQMBYVPZ-UHFFFAOYSA-N 5-fluoro-2-[(4-methylphenyl)methoxy]pyrimidin-4-amine Chemical compound C1=CC(C)=CC=C1COC1=NC=C(F)C(N)=N1 CGRCPZUQMBYVPZ-UHFFFAOYSA-N 0.000 claims description 2
- JMBYFCMNFXBELT-UHFFFAOYSA-N 5-methyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound NC1=C(CCCCCCCC)C(C)=NC2=NC=NN21 JMBYFCMNFXBELT-UHFFFAOYSA-N 0.000 claims description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 2
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- 239000005810 Metrafenone Substances 0.000 claims description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 claims description 2
- 239000005847 Triazoxide Substances 0.000 claims description 2
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- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 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 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YNWVFADWVLCOPU-MAUPQMMJSA-N uniconazole P Chemical compound C1=NC=NN1/C([C@@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MAUPQMMJSA-N 0.000 description 1
- 229960004740 voriconazole Drugs 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 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 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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
- A01N63/10—Animals; 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
- 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
- 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
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
-
- 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
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Microbiology (AREA)
- Virology (AREA)
- Biotechnology (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12004160 | 2012-05-30 | ||
| EP12197942 | 2012-12-19 | ||
| PCT/EP2013/061016 WO2013178653A1 (en) | 2012-05-30 | 2013-05-29 | Composition comprising a biological control agent and a fungicide selected from inhibitors of amino acid or protein biosynthesis, inhibitors of atp production and inhibitors of the cell wall synthesis |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2737754T3 true ES2737754T3 (es) | 2020-01-15 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES13726742T Active ES2737754T3 (es) | 2012-05-30 | 2013-05-29 | 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 |
Country Status (17)
| Country | Link |
|---|---|
| US (3) | US9380787B2 (OSRAM) |
| EP (2) | EP2854552B1 (OSRAM) |
| KR (1) | KR20150023474A (OSRAM) |
| CN (2) | CN104507317B (OSRAM) |
| AR (1) | AR091199A1 (OSRAM) |
| BR (1) | BR112014029224A2 (OSRAM) |
| CO (1) | CO7210304A2 (OSRAM) |
| EC (1) | ECSP14029008A (OSRAM) |
| ES (1) | ES2737754T3 (OSRAM) |
| HU (1) | HUE044560T2 (OSRAM) |
| IN (1) | IN2014DN10220A (OSRAM) |
| MX (1) | MX356530B (OSRAM) |
| PH (1) | PH12014502654A1 (OSRAM) |
| PL (1) | PL2854552T3 (OSRAM) |
| PT (1) | PT2854552T (OSRAM) |
| WO (1) | WO2013178653A1 (OSRAM) |
| ZA (1) | ZA201408567B (OSRAM) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CA2874916A1 (en) | 2012-05-30 | 2013-12-05 | Bayer Cropscience Ag | Composition comprising a biological control agent and a fungicide |
| EP3243387A3 (en) | 2012-05-30 | 2017-12-13 | Bayer CropScience Aktiengesellschaft | Compositions comprising a biological control agent and an insecticide |
| BR112014029689A2 (pt) | 2012-05-30 | 2017-06-27 | Bayer Cropscience Ag | composição que compreende um agente de controle biológico e um fungicida |
| IN2014DN09381A (OSRAM) | 2012-05-30 | 2015-07-17 | Bayer Cropscience Ag | |
| CN104735987B (zh) | 2012-05-30 | 2018-12-07 | 拜尔农作物科学股份公司 | 包含生物防治剂和杀真菌剂的组合物 |
| CN107926985B (zh) | 2012-05-30 | 2021-02-02 | 拜尔农作物科学股份公司 | 包含生物防治剂和杀真菌剂的组合物 |
| NZ701664A (en) | 2012-05-30 | 2016-09-30 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
| CN104363758B (zh) | 2012-05-30 | 2017-02-08 | 拜耳作物科学公司 | 包含生物防治剂和杀虫剂的组合物 |
| US9907312B2 (en) | 2012-05-30 | 2018-03-06 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
| NZ701680A (en) | 2012-05-30 | 2016-11-25 | Bayer Cropscience Ag | Compositiions comprising a biological control agent and an insecticide |
| NZ742943A (en) | 2012-05-30 | 2019-04-26 | 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 |
| EP2865265A1 (en) | 2014-02-13 | 2015-04-29 | Bayer CropScience AG | Active compound combinations comprising phenylamidine compounds and biological control agents |
| EP2865267A1 (en) | 2014-02-13 | 2015-04-29 | Bayer CropScience AG | Active compound combinations comprising phenylamidine compounds and biological control agents |
| CN103749542B (zh) * | 2014-02-21 | 2015-06-10 | 江苏省农业科学院 | 解淀粉芽孢杆菌井冈霉素复配生物杀菌剂及其应用 |
| WO2016109424A1 (en) | 2014-12-29 | 2016-07-07 | Fmc Corporation | Microbial compositions and methods of use for benefiting plant growth and treating plant disease |
| JPWO2016194971A1 (ja) * | 2015-06-01 | 2018-03-15 | 石原産業株式会社 | 殺菌剤組成物及び植物病害の防除方法 |
| WO2019108879A1 (en) * | 2017-11-30 | 2019-06-06 | Boragen, Inc. | Combinatorial compositions of benzoxaboroles and biologic agents |
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| CN107926985B (zh) | 2012-05-30 | 2021-02-02 | 拜尔农作物科学股份公司 | 包含生物防治剂和杀真菌剂的组合物 |
| NZ701664A (en) | 2012-05-30 | 2016-09-30 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
| AR091197A1 (es) | 2012-05-30 | 2015-01-21 | Bayer Cropscience Ag | Composicion que comprende un agente de control biologico y un fungicida |
| NZ742943A (en) | 2012-05-30 | 2019-04-26 | 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 |
| NZ701680A (en) | 2012-05-30 | 2016-11-25 | Bayer Cropscience Ag | Compositiions comprising a biological control agent and an insecticide |
| IN2014DN09381A (OSRAM) | 2012-05-30 | 2015-07-17 | Bayer Cropscience Ag | |
| BR112014029689A2 (pt) | 2012-05-30 | 2017-06-27 | Bayer Cropscience Ag | composição que compreende um agente de controle biológico e um fungicida |
| US9907312B2 (en) | 2012-05-30 | 2018-03-06 | Bayer Cropscience Ag | Compositions comprising a biological control agent and an insecticide |
-
2013
- 2013-05-29 KR KR20147036237A patent/KR20150023474A/ko not_active Withdrawn
- 2013-05-29 ES ES13726742T patent/ES2737754T3/es active Active
- 2013-05-29 PL PL13726742T patent/PL2854552T3/pl unknown
- 2013-05-29 CN CN201380040229.1A patent/CN104507317B/zh not_active Expired - Fee Related
- 2013-05-29 CN CN201810339392.2A patent/CN108669088A/zh active Pending
- 2013-05-29 EP EP13726742.3A patent/EP2854552B1/en active Active
- 2013-05-29 PT PT13726742T patent/PT2854552T/pt unknown
- 2013-05-29 IN IN10220DEN2014 patent/IN2014DN10220A/en unknown
- 2013-05-29 AR ARP130101878 patent/AR091199A1/es unknown
- 2013-05-29 WO PCT/EP2013/061016 patent/WO2013178653A1/en not_active Ceased
- 2013-05-29 US US14/404,016 patent/US9380787B2/en active Active
- 2013-05-29 MX MX2014014354A patent/MX356530B/es active IP Right Grant
- 2013-05-29 BR BR112014029224A patent/BR112014029224A2/pt not_active Application Discontinuation
- 2013-05-29 HU HUE13726742 patent/HUE044560T2/hu unknown
- 2013-05-29 EP EP18154590.6A patent/EP3360418A1/en not_active Withdrawn
-
2014
- 2014-06-27 US US14/318,130 patent/US20140309107A1/en not_active Abandoned
- 2014-11-21 ZA ZA2014/08567A patent/ZA201408567B/en unknown
- 2014-11-26 CO CO14260412A patent/CO7210304A2/es unknown
- 2014-11-27 PH PH12014502654A patent/PH12014502654A1/en unknown
- 2014-11-27 EC ECIEPI201429008A patent/ECSP14029008A/es unknown
-
2016
- 2016-06-01 US US15/170,484 patent/US9706777B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| AR091199A1 (es) | 2015-01-21 |
| US9380787B2 (en) | 2016-07-05 |
| ZA201408567B (en) | 2019-03-27 |
| BR112014029224A2 (pt) | 2017-06-27 |
| US20150148229A1 (en) | 2015-05-28 |
| US9706777B2 (en) | 2017-07-18 |
| US20140309107A1 (en) | 2014-10-16 |
| EP2854552B1 (en) | 2019-05-08 |
| PT2854552T (pt) | 2019-07-25 |
| US20160270406A1 (en) | 2016-09-22 |
| HUE044560T2 (hu) | 2019-11-28 |
| ECSP14029008A (es) | 2015-12-31 |
| MX356530B (es) | 2018-06-01 |
| WO2013178653A1 (en) | 2013-12-05 |
| IN2014DN10220A (OSRAM) | 2015-08-07 |
| CN104507317B (zh) | 2019-11-15 |
| PH12014502654A1 (en) | 2015-01-21 |
| CO7210304A2 (es) | 2015-03-09 |
| EP2854552A1 (en) | 2015-04-08 |
| CN104507317A (zh) | 2015-04-08 |
| KR20150023474A (ko) | 2015-03-05 |
| PL2854552T3 (pl) | 2019-11-29 |
| CN108669088A (zh) | 2018-10-19 |
| MX2014014354A (es) | 2015-02-05 |
| EP3360418A1 (en) | 2018-08-15 |
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