CA2888600C - Active compound combinations comprising carboxamide derivatives - Google Patents
Active compound combinations comprising carboxamide derivatives Download PDFInfo
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- CA2888600C CA2888600C CA2888600A CA2888600A CA2888600C CA 2888600 C CA2888600 C CA 2888600C CA 2888600 A CA2888600 A CA 2888600A CA 2888600 A CA2888600 A CA 2888600A CA 2888600 C CA2888600 C CA 2888600C
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 208
- 229940053202 antiepileptics carboxamide derivative Drugs 0.000 title description 2
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- 235000013399 edible fruits Nutrition 0.000 claims description 21
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 claims description 17
- 239000005562 Glyphosate Substances 0.000 claims description 16
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- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 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
- 238000009423 ventilation Methods 0.000 description 1
- 238000009369 viticulture Methods 0.000 description 1
- 239000004552 water soluble powder Substances 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- MBMQEIFVQACCCH-QBODLPLBSA-N zearalenone Chemical compound O=C1O[C@@H](C)CCCC(=O)CCC\C=C\C2=CC(O)=CC(O)=C21 MBMQEIFVQACCCH-QBODLPLBSA-N 0.000 description 1
- 229940023877 zeatin Drugs 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/04—Sulfonic acids; Derivatives thereof
- A01N41/06—Sulfonic acid amides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12356025.2 | 2012-10-19 | ||
| EP12356025 | 2012-10-19 | ||
| US201261730251P | 2012-11-27 | 2012-11-27 | |
| US61/730,251 | 2012-11-27 | ||
| PCT/EP2013/071694 WO2014060502A1 (en) | 2012-10-19 | 2013-10-17 | Active compound combinations comprising carboxamide derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2888600A1 CA2888600A1 (en) | 2014-04-24 |
| CA2888600C true CA2888600C (en) | 2021-08-10 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2888600A Active CA2888600C (en) | 2012-10-19 | 2013-10-17 | Active compound combinations comprising carboxamide derivatives |
Country Status (10)
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| EP (1) | EP2908639A1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP6153619B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN105357968A (cg-RX-API-DMAC7.html) |
| AR (1) | AR093069A1 (cg-RX-API-DMAC7.html) |
| AU (2) | AU2013333916B2 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2888600C (cg-RX-API-DMAC7.html) |
| EA (1) | EA026839B1 (cg-RX-API-DMAC7.html) |
| UA (1) | UA114822C2 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2014060502A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102134565B1 (ko) | 2012-10-19 | 2020-07-16 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 카르복사미드 또는 티오카르복사미드 유도체를 사용한 살진균제에 내성을 가지는 진균에 대항하는 식물의 처리 방법 |
| CN105357967B (zh) * | 2012-10-19 | 2019-02-19 | 拜尔农科股份公司 | 使用羧酰胺衍生物促进植物生长的方法 |
| EA025862B1 (ru) * | 2012-10-19 | 2017-02-28 | Байер Кропсайенс Аг | Способ повышения устойчивости к абиотическому стрессу в растениях с использованием производных карбоксамида или тиокарбоксамида |
| KR102123218B1 (ko) | 2012-10-19 | 2020-06-16 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 카르복사미드 유도체 및 생물학적 제어제를 포함하는 활성 화합물 조합물 |
| WO2016174042A1 (en) | 2015-04-27 | 2016-11-03 | BASF Agro B.V. | Pesticidal compositions |
| AR104687A1 (es) * | 2015-05-19 | 2017-08-09 | Bayer Cropscience Ag | Método para tratar las enfermedades roya del café, mancha negra de los cítricos, sarna de los cítricos y sigatoka negra de la banana |
| WO2017207368A1 (en) | 2016-06-02 | 2017-12-07 | BASF Agro B.V. | Fungicidal compositions |
| WO2018069110A1 (en) | 2016-10-10 | 2018-04-19 | Basf Se | Pesticidal mixtures |
| PL3522714T3 (pl) | 2016-10-10 | 2024-03-04 | Basf Se | Mieszaniny szkodnikobójcze |
| EP3522716A1 (en) | 2016-10-10 | 2019-08-14 | Basf Se | Pesticidal mixtures |
| WO2020007646A1 (en) | 2018-07-02 | 2020-01-09 | Basf Se | Pesticidal mixtures |
| EP3698634A1 (en) | 2019-02-25 | 2020-08-26 | Basf Se | Pesticidal mixtures |
| EP4066643A1 (en) | 2021-03-30 | 2022-10-05 | Basf Se | Pesticidal mixtures |
Family Cites Families (336)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2036008A (en) | 1934-11-07 | 1936-03-31 | White Martin Henry | Plug fuse |
| US2289060A (en) | 1940-03-12 | 1942-07-07 | Merkle Corp | Method of and apparatus for utilizing dry ice |
| DE2417487C2 (de) | 1974-04-10 | 1983-01-20 | Hoechst Ag, 6000 Frankfurt | Benzyl-phenoxyalkancarbonsäuren, deren Derivate und Verfahren zu ihrer Herstellung |
| DE2433067B2 (de) | 1974-07-10 | 1977-11-24 | a- [4-(4" Trifluormethylphenoxy)-phenoxy] -propionsäuren und deren Derivate, Verfahren zu ihrer Herstellung und diese enthaltende herbizide Mittel Hoechst AG, 6000 Frankfurt | Alpha- eckige klammer auf 4-(4' trifluormethylphenoxy)-phenoxy eckige klammer zu -propionsaeuren und deren derivate, verfahren zu ihrer herstellung und diese enthaltende herbizide mittel |
| DE2601548C2 (de) | 1976-01-16 | 1984-01-26 | Hoechst Ag, 6230 Frankfurt | 2-[4-(2'-Chlor-4'-bromphenoxy)-phenoxy]-propionsäure und Derivate sowie diese enthaltende herbizide Mittel |
| DE2640730C2 (de) | 1976-09-10 | 1983-08-25 | Hoechst Ag, 6230 Frankfurt | Benzoxazolyloxy- und Benzothiazolyloxy-phenoxy-Verbindungen und diese enthaltende herbizide Mittel |
| JPS55500010A (cg-RX-API-DMAC7.html) | 1977-12-23 | 1980-01-17 | ||
| DE2961917D1 (en) | 1978-01-18 | 1982-03-11 | Ciba Geigy Ag | Herbicidal active unsaturated esters of 4- (3',5'-dihalogenpyridyl-(2')-oxy)-alpha-phenoxy propionic acids, process for their preparation, herbicidal compositions containing them and their use |
| DE2964580D1 (en) | 1978-03-01 | 1983-03-03 | Ici Plc | Herbicidal pyridine compounds and herbicidal compositions containing them |
| DE2834251A1 (de) | 1978-08-04 | 1980-03-06 | Huels Chemische Werke Ag | Verfahren zur reinigung von tertiaeren aminen |
| US4272417A (en) | 1979-05-22 | 1981-06-09 | Cargill, Incorporated | Stable protective seed coating |
| US4245432A (en) | 1979-07-25 | 1981-01-20 | Eastman Kodak Company | Seed coatings |
| AU591450B2 (en) | 1981-10-16 | 1989-12-07 | E.I. Du Pont De Nemours And Company | Novel phenyl-substituted sulfonamides |
| MA19709A1 (fr) | 1982-02-17 | 1983-10-01 | Ciba Geigy Ag | Application de derives de quinoleine a la protection des plantes cultivees . |
| DE3382743D1 (de) | 1982-05-07 | 1994-05-11 | Ciba Geigy | Verwendung von Chinolinderivaten zum Schützen von Kulturpflanzen. |
| DE3324802A1 (de) | 1983-07-09 | 1985-01-17 | Hoechst Ag, 6230 Frankfurt | Neue n-alkoxy- und n- alkylsulfonylaminosulfonylharnstoffe, und neue (pyrimido) triazino-thiadiazinoxide als vorprodukte |
| US4808750A (en) | 1983-09-01 | 1989-02-28 | The Dow Chemical Company | Fluorophenoxyphenoxypropionates and derivatives thereof |
| US5331107A (en) | 1984-03-06 | 1994-07-19 | Mgi Pharma, Inc. | Herbicide resistance in plants |
| US5304732A (en) | 1984-03-06 | 1994-04-19 | Mgi Pharma, Inc. | Herbicide resistance in plants |
| US4761373A (en) | 1984-03-06 | 1988-08-02 | Molecular Genetics, Inc. | Herbicide resistance in plants |
| DE3525205A1 (de) | 1984-09-11 | 1986-03-20 | Hoechst Ag, 6230 Frankfurt | Pflanzenschuetzende mittel auf basis von 1,2,4-triazolderivaten sowie neue derivate des 1,2,4-triazols |
| EP0191736B1 (de) | 1985-02-14 | 1991-07-17 | Ciba-Geigy Ag | Verwendung von Chinolinderivaten zum Schützen von Kulturpflanzen |
| EP0242236B2 (en) | 1986-03-11 | 1996-08-21 | Plant Genetic Systems N.V. | Plant cells resistant to glutamine synthetase inhibitors, made by genetic engineering |
| AU587539B2 (en) | 1986-06-14 | 1989-08-17 | Ihara Chemical Industry Co. Ltd. | Picolinic acid derivatives and herbicidal compositions |
| US5276268A (en) | 1986-08-23 | 1994-01-04 | Hoechst Aktiengesellschaft | Phosphinothricin-resistance gene, and its use |
| US5273894A (en) | 1986-08-23 | 1993-12-28 | Hoechst Aktiengesellschaft | Phosphinothricin-resistance gene, and its use |
| US5637489A (en) | 1986-08-23 | 1997-06-10 | Hoechst Aktiengesellschaft | Phosphinothricin-resistance gene, and its use |
| US5013659A (en) | 1987-07-27 | 1991-05-07 | E. I. Du Pont De Nemours And Company | Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase |
| US5378824A (en) | 1986-08-26 | 1995-01-03 | E. I. Du Pont De Nemours And Company | Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase |
| US5605011A (en) | 1986-08-26 | 1997-02-25 | E. I. Du Pont De Nemours And Company | Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase |
| DE3633840A1 (de) | 1986-10-04 | 1988-04-14 | Hoechst Ag | Phenylpyrazolcarbonsaeurederivate, ihre herstellung und verwendung als pflanzenwachstumsregulatoren und safener |
| EP0274634A1 (en) | 1986-12-04 | 1988-07-20 | Stauffer Chemical Company | Synergistic herbicide compositions and method of application |
| US4808430A (en) | 1987-02-27 | 1989-02-28 | Yazaki Corporation | Method of applying gel coating to plant seeds |
| US5638637A (en) | 1987-12-31 | 1997-06-17 | Pioneer Hi-Bred International, Inc. | Production of improved rapeseed exhibiting an enhanced oleic acid content |
| DE122008000064I2 (de) | 1988-01-06 | 2011-06-16 | Chemtura Corp N D Ges D Staates Delaware | Herbizide Heterozyklisch-alkylen-Chinoxalinyloxyphenoxy Propansäureester. |
| DE3808896A1 (de) | 1988-03-17 | 1989-09-28 | Hoechst Ag | Pflanzenschuetzende mittel auf basis von pyrazolcarbonsaeurederivaten |
| GB8810120D0 (en) | 1988-04-28 | 1988-06-02 | Plant Genetic Systems Nv | Transgenic nuclear male sterile plants |
| DE3817192A1 (de) | 1988-05-20 | 1989-11-30 | Hoechst Ag | 1,2,4-triazolderivate enthaltende pflanzenschuetzende mittel sowie neue derivate des 1,2,4-triazols |
| US5084082A (en) | 1988-09-22 | 1992-01-28 | E. I. Du Pont De Nemours And Company | Soybean plants with dominant selectable trait for herbicide resistance |
| US6013861A (en) | 1989-05-26 | 2000-01-11 | Zeneca Limited | Plants and processes for obtaining them |
| EP1090999B1 (en) | 1989-08-10 | 2011-01-19 | Bayer BioScience N.V. | Plant with modified flowers |
| DE3939010A1 (de) | 1989-11-25 | 1991-05-29 | Hoechst Ag | Isoxazoline, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschuetzende mittel |
| DE3939503A1 (de) | 1989-11-30 | 1991-06-06 | Hoechst Ag | Neue pyrazoline zum schutz von kulturpflanzen gegenueber herbiziden |
| DE4000503A1 (de) | 1990-01-10 | 1991-07-11 | Hoechst Ag | Pyridylsulfonylharnstoffe als herbizide und pflanzenwachstumsregulatoren |
| US5739082A (en) | 1990-02-02 | 1998-04-14 | Hoechst Schering Agrevo Gmbh | Method of improving the yield of herbicide-resistant crop plants |
| US5908810A (en) | 1990-02-02 | 1999-06-01 | Hoechst Schering Agrevo Gmbh | Method of improving the growth of crop plants which are resistant to glutamine synthetase inhibitors |
| AU7463791A (en) | 1990-03-14 | 1991-10-10 | James L. Ahle | Herbicidal compositions of aroylated 1,3-dicarbonyl or 1,3,5-tricarbonyl cyclohexane herbicides and an antidote system therefor |
| AU639319B2 (en) | 1990-04-04 | 1993-07-22 | Pioneer Hi-Bred International, Inc. | Production of improved rapeseed exhibiting a reduced saturated fatty acid content |
| US5198599A (en) | 1990-06-05 | 1993-03-30 | Idaho Resarch Foundation, Inc. | Sulfonylurea herbicide resistance in plants |
| ES2173077T3 (es) | 1990-06-25 | 2002-10-16 | Monsanto Technology Llc | Plantas que toleran glifosato. |
| US6395966B1 (en) | 1990-08-09 | 2002-05-28 | Dekalb Genetics Corp. | Fertile transgenic maize plants containing a gene encoding the pat protein |
| JPH04103574A (ja) | 1990-08-22 | 1992-04-06 | Kumiai Chem Ind Co Ltd | ピリミジン誘導体及び除草剤 |
| FR2667078B1 (fr) | 1990-09-21 | 1994-09-16 | Agronomique Inst Nat Rech | Sequence d'adn conferant une sterilite male cytoplasmique, genome mitochondrial, mitochondrie et plante contenant cette sequence, et procede de preparation d'hybrides. |
| EP0492366B1 (de) | 1990-12-21 | 1997-03-26 | Hoechst Schering AgrEvo GmbH | Neue 5-Chlorchinolin-8-oxyalkancarbonsäurederivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Antidots von Herbiziden |
| ZA92970B (en) | 1991-02-12 | 1992-10-28 | Hoechst Ag | Arylsulfonylureas,processes for their preparation,and their use as herbicides and growth regulators |
| DE4104782B4 (de) | 1991-02-13 | 2006-05-11 | Bayer Cropscience Gmbh | Neue Plasmide, enthaltend DNA-Sequenzen, die Veränderungen der Karbohydratkonzentration und Karbohydratzusammensetzung in Pflanzen hervorrufen, sowie Pflanzen und Pflanzenzellen enthaltend dieses Plasmide |
| US5731180A (en) | 1991-07-31 | 1998-03-24 | American Cyanamid Company | Imidazolinone resistant AHAS mutants |
| US6270828B1 (en) | 1993-11-12 | 2001-08-07 | Cargrill Incorporated | Canola variety producing a seed with reduced glucosinolates and linolenic acid yielding an oil with low sulfur, improved sensory characteristics and increased oxidative stability |
| TW259690B (cg-RX-API-DMAC7.html) | 1992-08-01 | 1995-10-11 | Hoechst Ag | |
| DE4227061A1 (de) | 1992-08-12 | 1994-02-17 | Inst Genbiologische Forschung | DNA-Sequenzen, die in der Pflanze die Bildung von Polyfructanen (Lävanen) hervorrufen, Plasmide enthaltend diese Sequenzen sowie Verfahren zur Herstellung transgener Pflanzen |
| GB9218185D0 (en) | 1992-08-26 | 1992-10-14 | Ici Plc | Novel plants and processes for obtaining them |
| WO1994009144A1 (en) | 1992-10-14 | 1994-04-28 | Zeneca Limited | Novel plants and processes for obtaining them |
| GB9223454D0 (en) | 1992-11-09 | 1992-12-23 | Ici Plc | Novel plants and processes for obtaining them |
| US5407897A (en) | 1993-03-03 | 1995-04-18 | American Cyanamid Company | Method for safening herbicides in crops using substituted benzopyran and tetrahydronaphthalene compounds |
| SK283509B6 (sk) | 1993-03-25 | 2003-08-05 | Novartis Ag | Pesticídne proteíny, kmene, ktoré ich obsahujú, nukleotidové sekvencie, ktoré ich kódujú, a rastliny nimi transformované |
| WO1994024849A1 (en) | 1993-04-27 | 1994-11-10 | Cargill, Incorporated | Non-hydrogenated canola oil for food applications |
| WO1995004826A1 (en) | 1993-08-09 | 1995-02-16 | Institut Für Genbiologische Forschung Berlin Gmbh | Debranching enzymes and dna sequences coding them, suitable for changing the degree of branching of amylopectin starch in plants |
| DE4330960C2 (de) | 1993-09-09 | 2002-06-20 | Aventis Cropscience Gmbh | Kombination von DNA-Sequenzen, die in Pflanzenzellen und Pflanzen die Bildung hochgradig amylosehaltiger Stärke ermöglichen, Verfahren zur Herstellung dieser Pflanzen und die daraus erhaltbare modifizierte Stärke |
| DE4331448A1 (de) | 1993-09-16 | 1995-03-23 | Hoechst Schering Agrevo Gmbh | Substituierte Isoxazoline, Verfahren zu deren Herstellung, diese enthaltende Mittel und deren Verwendung als Safener |
| EP0675198A4 (en) | 1993-10-01 | 1996-01-10 | Mitsubishi Chem Ind | Gene that identifies sterile plant cytoplasm and process for preparing hybrid plant by using the same. |
| AU692791B2 (en) | 1993-10-12 | 1998-06-18 | Agrigenetics, Inc. | Brassica napus variety AG019 |
| HUT75075A (en) | 1993-11-09 | 1997-04-28 | Du Pont | Transgenic fructan accumulating crops and methods for their production |
| CA2186399C (en) | 1994-03-25 | 2001-09-04 | David Cooke | Method for producing altered starch from potato plants |
| KR100352532B1 (ko) | 1994-05-18 | 2004-02-18 | 플란테크 비오테크놀로지 게엠베하, 포르슝 운트 엔트비클룽 | 식물,진균류및미생물에서선형알파-1,4글루칸의형성을용이하게할수있는효소를코딩하는dna서열 |
| US5824790A (en) | 1994-06-21 | 1998-10-20 | Zeneca Limited | Modification of starch synthesis in plants |
| CN1156951A (zh) | 1994-06-21 | 1997-08-13 | 曾尼卡有限公司 | 新的植物及其制备方法 |
| NL1000064C1 (nl) | 1994-07-08 | 1996-01-08 | Stichting Scheikundig Onderzoe | Produktie van oligosacchariden in transgene planten. |
| DE4441408A1 (de) | 1994-11-10 | 1996-05-15 | Inst Genbiologische Forschung | DNA-Sequenzen aus Solanum tuberosum kodierend Enzyme, die an der Stärkesynthese beteiligt sind, Plasmide, Bakterien, Pflanzenzellen und transgene Pflanzen enhaltend diese Sequenzen |
| DE4447387A1 (de) | 1994-12-22 | 1996-06-27 | Inst Genbiologische Forschung | Debranching-Enzyme aus Pflanzen und DNA-Sequenzen kodierend diese Enzyme |
| AU4634396A (en) | 1995-01-06 | 1996-07-24 | Centrum Voor Plantenveredelings- En Reproduktieonderzoek (Cpro - Dlo) | Dna sequences encoding carbohydrate polymer synthesizing enzymes and method for producing transgenic plants |
| CN1071757C (zh) | 1995-02-24 | 2001-09-26 | 巴斯福股份公司 | 吡唑基苯甲酰基衍生物 |
| DE19509695A1 (de) | 1995-03-08 | 1996-09-12 | Inst Genbiologische Forschung | Verfahren zur Herstellung einer modifizieren Stärke in Pflanzen, sowie die aus den Pflanzen isolierbare modifizierte Stärke |
| JP4469422B2 (ja) | 1995-04-20 | 2010-05-26 | アメリカン シアナミド コンパニー | 構造に基づきデザインされた除草剤耐性生産物 |
| US5853973A (en) | 1995-04-20 | 1998-12-29 | American Cyanamid Company | Structure based designed herbicide resistant products |
| DE69637153T8 (de) | 1995-05-05 | 2008-07-24 | National Starch And Chemical Investment Holding Corporation, New Castle | Verbesserungen in oder in bezug auf pflanzenstärkeverbindungen |
| FR2734842B1 (fr) | 1995-06-02 | 1998-02-27 | Rhone Poulenc Agrochimie | Sequence adn d'un gene de l'hydroxy-phenyl pyruvate dioxygenase et obtention de plantes contenant un gene de l'hydroxy-phenyl pyruvate dioxygenase, tolerantes a certains herbicides |
| US6284479B1 (en) | 1995-06-07 | 2001-09-04 | Pioneer Hi-Bred International, Inc. | Substitutes for modified starch and latexes in paper manufacture |
| US5712107A (en) | 1995-06-07 | 1998-01-27 | Pioneer Hi-Bred International, Inc. | Substitutes for modified starch and latexes in paper manufacture |
| GB9513881D0 (en) | 1995-07-07 | 1995-09-06 | Zeneca Ltd | Improved plants |
| FR2736926B1 (fr) | 1995-07-19 | 1997-08-22 | Rhone Poulenc Agrochimie | 5-enol pyruvylshikimate-3-phosphate synthase mutee, gene codant pour cette proteine et plantes transformees contenant ce gene |
| DK1435205T3 (da) | 1995-09-19 | 2010-03-29 | Bayer Bioscience Gmbh | Fremgangsmåde til fremstilling af en modificeret stivelse |
| GB9524938D0 (en) | 1995-12-06 | 1996-02-07 | Zeneca Ltd | Modification of starch synthesis in plants |
| DE19601365A1 (de) | 1996-01-16 | 1997-07-17 | Planttec Biotechnologie Gmbh | Nucleinsäuremoleküle aus Pflanzen codierend Enzyme, die an der Stärkesynthese beteiligt sind |
| DE19608918A1 (de) | 1996-03-07 | 1997-09-11 | Planttec Biotechnologie Gmbh | Nucleinsäuremoleküle, die neue Debranching-Enzyme aus Mais codieren |
| US5773704A (en) | 1996-04-29 | 1998-06-30 | Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College | Herbicide resistant rice |
| DE19618125A1 (de) | 1996-05-06 | 1997-11-13 | Planttec Biotechnologie Gmbh | Nucleinsäuremoleküle, die neue Debranching-Enzyme aus Kartoffel codieren |
| DE19619918A1 (de) | 1996-05-17 | 1997-11-20 | Planttec Biotechnologie Gmbh | Nucleinsäuremoleküle codierend lösliche Stärkesynthasen aus Mais |
| CZ389098A3 (cs) | 1996-05-29 | 1999-02-17 | Hoechst Schering Agrevo Gmbh | Molekuly nukleové kyseliny kódující enzymy z pšenice účastnící se syntézy škrobu |
| WO1997047806A1 (en) | 1996-06-12 | 1997-12-18 | Pioneer Hi-Bred International, Inc. | Substitutes for modified starch in paper manufacture |
| AU729286B2 (en) | 1996-06-12 | 2001-02-01 | Pioneer Hi-Bred International, Inc. | Substitutes for modified starch in paper manufacture |
| JP2000512349A (ja) | 1996-06-12 | 2000-09-19 | パイオニア ハイ―ブレッド インターナショナル，インコーポレイテッド | 製紙における改変澱粉の代用品 |
| US5876739A (en) | 1996-06-13 | 1999-03-02 | Novartis Ag | Insecticidal seed coating |
| AUPO069996A0 (en) | 1996-06-27 | 1996-07-18 | Australian National University, The | Manipulation of plant cellulose |
| US5850026A (en) | 1996-07-03 | 1998-12-15 | Cargill, Incorporated | Canola oil having increased oleic acid and decreased linolenic acid content |
| US5773702A (en) | 1996-07-17 | 1998-06-30 | Board Of Trustees Operating Michigan State University | Imidazolinone herbicide resistant sugar beet plants |
| GB9623095D0 (en) | 1996-11-05 | 1997-01-08 | Nat Starch Chem Invest | Improvements in or relating to starch content of plants |
| US6232529B1 (en) | 1996-11-20 | 2001-05-15 | Pioneer Hi-Bred International, Inc. | Methods of producing high-oil seed by modification of starch levels |
| DE19653176A1 (de) | 1996-12-19 | 1998-06-25 | Planttec Biotechnologie Gmbh | Neue Nucleinsäuremoleküle aus Mais und ihre Verwendung zur Herstellung einer modifizierten Stärke |
| CA2193938A1 (en) | 1996-12-24 | 1998-06-24 | David G. Charne | Oilseed brassica containing an improved fertility restorer gene for ogura cytoplasmic male sterility |
| US5981840A (en) | 1997-01-24 | 1999-11-09 | Pioneer Hi-Bred International, Inc. | Methods for agrobacterium-mediated transformation |
| DE19708774A1 (de) | 1997-03-04 | 1998-09-17 | Max Planck Gesellschaft | Nucleinsäuremoleküle codierend Enzyme die Fructosylpolymeraseaktivität besitzen |
| DE19709775A1 (de) | 1997-03-10 | 1998-09-17 | Planttec Biotechnologie Gmbh | Nucleinsäuremoleküle codierend Stärkephosphorylase aus Mais |
| CA2888685C (en) | 1997-04-03 | 2017-05-09 | T. Michael Spencer | Glyphosate resistant maize lines |
| GB9718863D0 (en) | 1997-09-06 | 1997-11-12 | Nat Starch Chem Invest | Improvements in or relating to stability of plant starches |
| DE19749122A1 (de) | 1997-11-06 | 1999-06-10 | Max Planck Gesellschaft | Nucleinsäuremoleküle codierend Enzyme, die Fructosyltransferaseaktivität besitzen |
| FR2770854B1 (fr) | 1997-11-07 | 2001-11-30 | Rhone Poulenc Agrochimie | Sequence adn d'un gene de l'hydroxy-phenyl pyruvate dioxygenase et obtention de plantes contenant un tel gene, tolerantes aux herbicides |
| FR2772789B1 (fr) | 1997-12-24 | 2000-11-24 | Rhone Poulenc Agrochimie | Procede de preparation enzymatique d'homogentisate |
| US20020016262A1 (en) | 1998-03-02 | 2002-02-07 | Idemitsu Kosan Co., Ltd. | Pyrazole derivatives and herbicides containing the same |
| EP1068333A1 (en) | 1998-04-09 | 2001-01-17 | E.I. Du Pont De Nemours And Company | Starch r1 phosphorylation protein homologs |
| DE19820608A1 (de) | 1998-05-08 | 1999-11-11 | Hoechst Schering Agrevo Gmbh | Nucleinsäuremoleküle codierend Enzyme aus Weizen, die an der Stärkesynthese beteiligt sind |
| DE19820607A1 (de) | 1998-05-08 | 1999-11-11 | Hoechst Schering Agrevo Gmbh | Nucleinsäuremoleküle codierend Enzyme aus Weizen, die an der Stärkesynthese beteiligt sind |
| DK1077955T3 (da) | 1998-05-11 | 2007-10-08 | Basf Ag | Fremgangsmåde til fremstilling af isoxazolin-3-yl-acylbenzen |
| DE59913709D1 (de) | 1998-05-13 | 2006-09-07 | Bayer Bioscience Gmbh | Transgene pflanzen mit veränderter aktivität eines plastidären adp/atp - translokators |
| DE19821614A1 (de) | 1998-05-14 | 1999-11-18 | Hoechst Schering Agrevo Gmbh | Sulfonylharnstoff-tolerante Zuckerrübenmutanten |
| DK1092033T3 (da) | 1998-06-15 | 2009-05-18 | Brunob Ii Bv | Forbedringer af eller vedrörende planter og planteprodukter |
| US6693185B2 (en) | 1998-07-17 | 2004-02-17 | Bayer Bioscience N.V. | Methods and means to modulate programmed cell death in eukaryotic cells |
| DE19836098A1 (de) | 1998-07-31 | 2000-02-03 | Hoechst Schering Agrevo Gmbh | Pflanzen, die eine modifizierte Stärke synthetisieren, Verfahren zur Herstellung der Pflanzen, ihre Verwendung sowie die modifizierte Stärke |
| DE19836099A1 (de) | 1998-07-31 | 2000-02-03 | Hoechst Schering Agrevo Gmbh | Nukleinsäuremoleküle kodierend für eine ß-Amylase, Pflanzen, die eine modifizierte Stärke synthetisieren, Verfahren zur Herstellung der Pflanzen, ihre Verwendung sowie die modifizierte Stärke |
| DE19836097A1 (de) | 1998-07-31 | 2000-02-03 | Hoechst Schering Agrevo Gmbh | Nukleinsäuremoleküle kodierend für eine alpha-Glukosidase, Pflanzen, die eine modifizierte Stärke synthetisieren, Verfahren zur Herstellung der Pflanzen, ihre Verwendung sowie die modifizierte Stärke |
| EP1108040A2 (en) | 1998-08-25 | 2001-06-20 | Pioneer Hi-Bred International, Inc. | Plant glutamine: fructose-6-phosphate amidotransferase nucleic acids |
| JP2002524080A (ja) | 1998-09-02 | 2002-08-06 | プランテック バイオテクノロジー ゲーエムベーハー | アミロスクラーゼをコードする核酸分子 |
| DE19924342A1 (de) | 1999-05-27 | 2000-11-30 | Planttec Biotechnologie Gmbh | Genetisch modifizierte Pflanzenzellen und Pflanzen mit erhöhter Aktivität eines Amylosucraseproteins und eines Verzweigungsenzyms |
| PL347223A1 (en) | 1998-10-09 | 2002-03-25 | Planttec Biotechnologie Gmbh | Nucleic acid molecules which code a branching enzyme from bacteria of the genus neisseria, and a method for producing α-1,6-branched α-1,4-glucans |
| AU1336200A (en) | 1998-11-03 | 2000-05-22 | Aventis Cropscience N.V. | Glufosinate tolerant rice |
| US6333449B1 (en) | 1998-11-03 | 2001-12-25 | Plant Genetic Systems, N.V. | Glufosinate tolerant rice |
| EP1131452B1 (en) | 1998-11-09 | 2014-01-22 | Bayer CropScience Aktiengesellschaft | Nucleic acid molecules from rice and their use for the production of modified starch |
| US6503904B2 (en) | 1998-11-16 | 2003-01-07 | Syngenta Crop Protection, Inc. | Pesticidal composition for seed treatment |
| US6531648B1 (en) | 1998-12-17 | 2003-03-11 | Syngenta Participations Ag | Grain processing method and transgenic plants useful therein |
| DE19905069A1 (de) | 1999-02-08 | 2000-08-10 | Planttec Biotechnologie Gmbh | Nucleinsäuremoleküle codierend Alternansucrase |
| US6323392B1 (en) | 1999-03-01 | 2001-11-27 | Pioneer Hi-Bred International, Inc. | Formation of brassica napus F1 hybrid seeds which exhibit a highly elevated oleic acid content and a reduced linolenic acid content in the endogenously formed oil of the seeds |
| IL146064A0 (en) | 1999-04-29 | 2002-07-25 | Marlow Foods Ltd | Herbicide resistant plants |
| CN1359423A (zh) | 1999-04-29 | 2002-07-17 | 辛甄塔有限公司 | 抗除草剂植物 |
| DE19926771A1 (de) | 1999-06-11 | 2000-12-14 | Aventis Cropscience Gmbh | Nukleinsäuremoleküle aus Weizen, transgene Pflanzenzellen und Pflanzen und deren Verwendung für die Herstellung modifizierter Stärke |
| DE19937348A1 (de) | 1999-08-11 | 2001-02-22 | Aventis Cropscience Gmbh | Nukleinsäuremoleküle aus Pflanzen codierend Enzyme, die an der Stärkesynthese beteiligt sind |
| DE19937643A1 (de) | 1999-08-12 | 2001-02-22 | Aventis Cropscience Gmbh | Transgene Zellen und Pflanzen mit veränderter Aktivität des GBSSI- und des BE-Proteins |
| AU7647000A (en) | 1999-08-20 | 2001-03-19 | Basf Plant Science Gmbh | Increasing the polysaccharide content in plants |
| US6423886B1 (en) | 1999-09-02 | 2002-07-23 | Pioneer Hi-Bred International, Inc. | Starch synthase polynucleotides and their use in the production of new starches |
| US6472588B1 (en) | 1999-09-10 | 2002-10-29 | Texas Tech University | Transgenic cotton plants with altered fiber characteristics transformed with a sucrose phosphate synthase nucleic acid |
| GB9921830D0 (en) | 1999-09-15 | 1999-11-17 | Nat Starch Chem Invest | Plants having reduced activity in two or more starch-modifying enzymes |
| AR025996A1 (es) | 1999-10-07 | 2002-12-26 | Valigen Us Inc | Plantas no transgenicas resistentes a los herbicidas. |
| US6509516B1 (en) | 1999-10-29 | 2003-01-21 | Plant Genetic Systems N.V. | Male-sterile brassica plants and methods for producing same |
| US6506963B1 (en) | 1999-12-08 | 2003-01-14 | Plant Genetic Systems, N.V. | Hybrid winter oilseed rape and methods for producing same |
| US6395485B1 (en) | 2000-01-11 | 2002-05-28 | Aventis Cropscience N.V. | Methods and kits for identifying elite event GAT-ZM1 in biological samples |
| CA2401093A1 (en) | 2000-03-09 | 2001-09-13 | Monsanto Technology Llc | Methods for making plants tolerant to glyphosate and compositions thereof |
| US6822146B2 (en) | 2000-03-09 | 2004-11-23 | E. I. Du Pont De Nemours And Company | Sulfonylurea-tolerant sunflower line M7 |
| HU228171B1 (en) | 2000-03-31 | 2013-01-28 | Bayer Cropscience Ag | Benzoylpyrazole derivatives and their use as herbicides |
| US6768044B1 (en) | 2000-05-10 | 2004-07-27 | Bayer Cropscience Sa | Chimeric hydroxyl-phenyl pyruvate dioxygenase, DNA sequence and method for obtaining plants containing such a gene, with herbicide tolerance |
| GT200100103A (es) | 2000-06-09 | 2002-02-21 | Nuevos herbicidas | |
| BRPI0100752B1 (pt) | 2000-06-22 | 2015-10-13 | Monsanto Co | moléculas e pares de moléculas de dna, processos para detectar molécula de dna e para criar um traço tolerante a glifosato em plantas de milho, bem como kit de detecção de dna |
| WO2002015695A2 (en) | 2000-08-25 | 2002-02-28 | Basf Aktiengesellschaft | Synergistic combination of a dihydrobenzothiophene herbicide and a photosystem ii inhibitor |
| US6713259B2 (en) | 2000-09-13 | 2004-03-30 | Monsanto Technology Llc | Corn event MON810 and compositions and methods for detection thereof |
| JP2004528808A (ja) | 2000-09-29 | 2004-09-24 | シンジェンタ リミテッド | 除草剤抵抗性植物 |
| US6660690B2 (en) | 2000-10-06 | 2003-12-09 | Monsanto Technology, L.L.C. | Seed treatment with combinations of insecticides |
| US6734340B2 (en) | 2000-10-23 | 2004-05-11 | Bayer Cropscience Gmbh | Monocotyledon plant cells and plants which synthesise modified starch |
| US6740488B2 (en) | 2000-10-25 | 2004-05-25 | Monsanto Technology Llc | Cotton event PV-GHGT07(1445) compositions and methods for detection thereof |
| ATE509110T1 (de) | 2000-10-30 | 2011-05-15 | Monsanto Technology Llc | Canola event pv-bngt(rt73), zusammensetzungen und verfahren zum nachweis davon |
| UA86918C2 (ru) | 2000-10-30 | 2009-06-10 | Вердиа, Инк. | Изолированный или рекомбинантный полинуклеотид, кодирующий полипептид, имеющий активность глифосат-n-ацетилтрансферазы (gat) |
| FR2815969B1 (fr) | 2000-10-30 | 2004-12-10 | Aventis Cropscience Sa | Plantes tolerantes aux herbicides par contournement de voie metabolique |
| WO2002044407A2 (en) | 2000-11-30 | 2002-06-06 | Ses Europe N.V. | Glyphosate resistant transgenic sugar beet characterised by a specific transgene insertion (t227-1), methods and primers for the detection of said insertion |
| WO2002046387A2 (en) | 2000-12-07 | 2002-06-13 | Syngenta Limited | Plant derived hydroxy phenyl pyruvate dioxygenases (hppd) resistant against triketone herbicides and transgenic plants containing these dioxygenases |
| CN1326996C (zh) | 2000-12-08 | 2007-07-18 | 联邦科学及工业研究组织 | 蔗糖合酶的基因表达在植物组织中的修饰及其用途 |
| US20020134012A1 (en) | 2001-03-21 | 2002-09-26 | Monsanto Technology, L.L.C. | Method of controlling the release of agricultural active ingredients from treated plant seeds |
| WO2002079410A2 (en) | 2001-03-30 | 2002-10-10 | Basf Plant Science Gmbh | Glucan chain length domains |
| EG26529A (en) | 2001-06-11 | 2014-01-27 | مونسانتو تكنولوجى ل ل سى | Prefixes for detection of DNA molecule in cotton plant MON15985 which gives resistance to damage caused by insect of squamous lepidoptera |
| DE60226508D1 (de) | 2001-06-12 | 2008-06-19 | Bayer Cropscience Gmbh | Transgene pflanzen die stärke mit hohem amylosegehalt herstellen |
| US6818807B2 (en) | 2001-08-06 | 2004-11-16 | Bayer Bioscience N.V. | Herbicide tolerant cotton plants having event EE-GH1 |
| WO2003013226A2 (en) | 2001-08-09 | 2003-02-20 | Cibus Genetics | Non-transgenic herbicide resistant plants |
| JP2005508166A (ja) | 2001-10-17 | 2005-03-31 | ビーエーエスエフ プラント サイエンス， ゲーエムベーハー | デンプン |
| AU2002361696A1 (en) | 2001-12-17 | 2003-06-30 | Syngenta Participations Ag | Novel corn event |
| DE10208132A1 (de) | 2002-02-26 | 2003-09-11 | Planttec Biotechnologie Gmbh | Verfahren zur Herstellung von Maispflanzen mit erhöhtem Blattstärkegehalt und deren Verwendung zur Herstellung von Maissilage |
| WO2003092360A2 (en) | 2002-04-30 | 2003-11-13 | Verdia, Inc. | Novel glyphosate-n-acetyltransferase (gat) genes |
| AU2003254099A1 (en) | 2002-07-29 | 2004-02-16 | Monsanto Technology, Llc | Corn event pv-zmir13 (mon863) plants and compositions and methods for detection thereof |
| FR2844142B1 (fr) | 2002-09-11 | 2007-08-17 | Bayer Cropscience Sa | Plantes transformees a biosynthese de prenylquinones amelioree |
| US20040142353A1 (en) | 2002-10-29 | 2004-07-22 | Cheung Wing Y. | Compositions and methods for identifying plants having increased tolerance to imidazolinone herbicides |
| GB0225129D0 (en) | 2002-10-29 | 2002-12-11 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
| WO2004053062A2 (en) | 2002-12-05 | 2004-06-24 | Monsanto Technology Llc | Bentgrass event asr-368 and compositions and methods for detection thereof |
| US20040110443A1 (en) | 2002-12-05 | 2004-06-10 | Pelham Matthew C. | Abrasive webs and methods of making the same |
| WO2004056999A1 (en) | 2002-12-19 | 2004-07-08 | Bayer Cropscience Gmbh | Plant cells and plants which synthesize a starch with an increased final viscosity |
| CN103088017B (zh) | 2003-02-12 | 2016-04-13 | 孟山都技术有限公司 | 棉花事件mon 88913及其组合物和检测方法 |
| US7335816B2 (en) | 2003-02-28 | 2008-02-26 | Kws Saat Ag | Glyphosate tolerant sugar beet |
| RS53441B (sr) | 2003-02-20 | 2014-12-31 | Kws Saat Ag | Glifozatno tolerantna šećerna repa |
| AU2004217810A1 (en) | 2003-03-07 | 2004-09-16 | Basf Plant Science Gmbh | Enhanced amylose production in plants |
| MXPA05010823A (es) | 2003-04-09 | 2005-12-05 | Bayer Bioscience Nv | Metodos y medios para incrementar la tolerancia de plantas a condiciones de fatiga. |
| SG155063A1 (en) | 2003-04-29 | 2009-09-30 | Pioneer Hi Bred Int | Novel glyphosate-n-acetyltransferase (gat) genes |
| DK1620571T3 (en) | 2003-05-02 | 2015-10-05 | Dow Agrosciences Llc | MAJS TD1507 and methods for detecting it |
| US20060282917A1 (en) | 2003-05-22 | 2006-12-14 | Syngenta Participations Ag | Modified starch, uses, methods for production thereof |
| AU2004243416B2 (en) | 2003-05-28 | 2009-06-11 | Basf Se | Wheat plants having increased tolerance to imidazolinone herbicides |
| EP1493328A1 (en) | 2003-07-04 | 2005-01-05 | Institut National De La Recherche Agronomique | Method of producing double low restorer lines of brassica napus having a good agronomic value |
| JP4816082B2 (ja) | 2003-07-31 | 2011-11-16 | 東洋紡績株式会社 | ヒアルロン酸生産植物 |
| EP1692285B1 (en) | 2003-08-15 | 2012-04-11 | Commonwealth Scientific and Industrial Research Organisation | Methods and means for altering fiber characteristics in fiber-producing plants |
| MXPA06002155A (es) | 2003-08-29 | 2007-01-25 | Inst Nac De Technologia Agrope | Plantas de arroz que tienen una tolerancia incrementada a los herbicidas de imidazolinona. |
| WO2005030941A1 (en) | 2003-09-30 | 2005-04-07 | Bayer Cropscience Gmbh | Plants with increased activity of a class 3 branching enzyme |
| ATE491784T1 (de) | 2003-09-30 | 2011-01-15 | Bayer Cropscience Ag | Pflanzen mit reduzierter aktivität eines klasse-3-verzweigungsenzyms |
| BRPI0416472A (pt) | 2003-12-01 | 2007-03-06 | Syngenta Participations Ag | plantas de algodão resistentes a insetos e métodos de detecção das mesmas |
| WO2005054480A2 (en) | 2003-12-01 | 2005-06-16 | Syngenta Participations Ag | Insect resistant cotton plants and methods of detecting the same |
| US7157281B2 (en) | 2003-12-11 | 2007-01-02 | Monsanto Technology Llc | High lysine maize compositions and event LY038 maize plants |
| HUE025703T2 (en) | 2003-12-15 | 2016-04-28 | Monsanto Technology Llc | MON88017 corn plant and compositions, and a method for detecting them |
| AR048026A1 (es) | 2004-03-05 | 2006-03-22 | Bayer Cropscience Gmbh | Procedimientos para la identificacion de proteinas con actividad enzimatica fosforiladora de almidon |
| ATE541042T1 (de) | 2004-03-05 | 2012-01-15 | Bayer Cropscience Ag | Pflanzen mit reduzierter aktivität des stärkephosphorylierenden enzyms phosphoglucan- wasser-dikinase |
| AR048024A1 (es) | 2004-03-05 | 2006-03-22 | Bayer Cropscience Gmbh | Plantas con actividad aumentada de distintas enzimas fosforilantes del almidon |
| AR048025A1 (es) | 2004-03-05 | 2006-03-22 | Bayer Cropscience Gmbh | Plantas con actividad aumentada de una enzima fosforilante del almidon |
| US7432082B2 (en) | 2004-03-22 | 2008-10-07 | Basf Ag | Methods and compositions for analyzing AHASL genes |
| NZ549466A (en) | 2004-03-25 | 2010-06-25 | Syngenta Participations Ag | Corn Event MIR604 |
| EP1737964A1 (en) | 2004-03-26 | 2007-01-03 | Dow AgroSciences LLC | Cry1f and cry1ac transgenic cotton lines and event-specific identification thereof |
| CA2570298A1 (en) | 2004-06-16 | 2006-01-19 | Basf Plant Science Gmbh | Polynucleotides encoding mature ahasl proteins for creating imidazolinone-tolerant plants |
| DE102004029763A1 (de) | 2004-06-21 | 2006-01-05 | Bayer Cropscience Gmbh | Pflanzen, die Amylopektin-Stärke mit neuen Eigenschaften herstellen |
| TR200700491T2 (tr) | 2004-07-30 | 2007-04-24 | Basf Agrochemical Products B.V. | Herbisitlere dayanıklı ayçiçeği bitkileri, herbisitlere dayanıklı asetohidroksiasit sintaz geniş altünite proteinlerini kodlayan polinükleotidler |
| US20070250946A1 (en) | 2004-08-04 | 2007-10-25 | Robert Ascenzi | Monocot Ahass Sequences and Methods of Use |
| EP1786908B1 (en) | 2004-08-18 | 2010-03-03 | Bayer CropScience AG | Plants with increased plastidic activity of r3 starch-phosphorylating enzyme |
| CA2578187C (en) | 2004-08-26 | 2015-08-04 | Dhara Vegetable Oil And Foods Company Limited | A novel cytoplasmic male sterility system for brassica species and its use for hybrid seed production in indian oilseed mustard brassica juncea |
| PT1805312E (pt) | 2004-09-23 | 2009-09-28 | Bayer Cropscience Ag | Processos e meios para produzir hialurano |
| US7323556B2 (en) | 2004-09-29 | 2008-01-29 | Pioneer Hi-Bred International, Inc. | Corn event DAS-59122-7 and methods for detection thereof |
| US8053636B2 (en) | 2004-10-29 | 2011-11-08 | Bayer Bioscience N.V. | Stress tolerant cotton plants |
| AR051690A1 (es) | 2004-12-01 | 2007-01-31 | Basf Agrochemical Products Bv | Mutacion implicada en el aumento de la tolerancia a los herbicidas imidazolinona en las plantas |
| EP1672075A1 (en) | 2004-12-17 | 2006-06-21 | Bayer CropScience GmbH | Transformed plant expressing a dextransucrase and synthesizing a modified starch |
| EP1679374A1 (en) | 2005-01-10 | 2006-07-12 | Bayer CropScience GmbH | Transformed plant expressing a mutansucrase and synthesizing a modified starch |
| CA2599381C (en) | 2005-03-16 | 2013-10-22 | Syngenta Participations Ag | Corn event 3272 and methods for detection thereof |
| JP2006304779A (ja) | 2005-03-30 | 2006-11-09 | Toyobo Co Ltd | ヘキソサミン高生産植物 |
| EP1707632A1 (de) | 2005-04-01 | 2006-10-04 | Bayer CropScience GmbH | Phosphorylierte waxy-Kartoffelstärke |
| CA2603944C (en) | 2005-04-08 | 2015-06-23 | Bayer Bioscience N.V. | Elite event a2704-12 comprising the integration of the phosphinothricin acetyltransferase (pat) gene into soybeans, and methods and kits for identifying such event in biological samples |
| EP1710315A1 (de) | 2005-04-08 | 2006-10-11 | Bayer CropScience GmbH | Hoch Phosphat Stärke |
| US8017756B2 (en) | 2005-04-11 | 2011-09-13 | Bayer Bioscience N.V. | Elite event A5547-127 and methods and kits for identifying such event in biological samples |
| PT1885176T (pt) | 2005-05-27 | 2016-11-28 | Monsanto Technology Llc | Evento mon89788 de soja e métodos para a sua deteção |
| US8759306B2 (en) | 2005-05-31 | 2014-06-24 | Devgen N.V. | RNAi for the control of insects and arachnids |
| US20100024077A1 (en) | 2005-06-02 | 2010-01-28 | Syngenta Participations Ag | Ce44-69d insecticidal cotton |
| WO2006128572A1 (en) | 2005-06-02 | 2006-12-07 | Syngenta Participations Ag | Ce46-02a insecticidal cotton |
| WO2006128568A2 (en) | 2005-06-02 | 2006-12-07 | Syngenta Participations Ag | T342-142, insecticidal transgenic cotton expressing cry1ab |
| CN101184847B (zh) | 2005-06-02 | 2015-02-25 | 先正达参股股份有限公司 | 表达cry1ab的杀昆虫转基因棉ce43-67b |
| WO2006128569A2 (en) | 2005-06-02 | 2006-12-07 | Syngenta Participations Ag | 1143-14a, insecticidal transgenic cotton expressing cry1ab |
| WO2006128570A1 (en) | 2005-06-02 | 2006-12-07 | Syngenta Participations Ag | 1143-51b insecticidal cotton |
| DE502006008090D1 (de) * | 2005-06-09 | 2010-11-25 | Bayer Cropscience Ag | Wirkstoffkombinationen |
| EP2110437A1 (en) | 2005-06-15 | 2009-10-21 | Bayer BioScience N.V. | Methods for increasing the resistance of plants to hypoxic conditions |
| BRPI0613153A2 (pt) | 2005-06-24 | 2010-12-21 | Bayer Bioscience Nv | métodos para alterar a reatividade de paredes celulares de plantas |
| AR054174A1 (es) | 2005-07-22 | 2007-06-06 | Bayer Cropscience Gmbh | Sobreexpresion de sintasa de almidon en vegetales |
| MX2008001839A (es) | 2005-08-08 | 2008-04-09 | Bayer Bioscience Nv | Plantas de algodon con tolerancia a herbicidas y metodos para identificar las mismas. |
| EP1931791B1 (en) | 2005-08-24 | 2012-02-08 | Pioneer-Hi-Bred International, Inc. | Methods and compositions for the expression of a polynucleotide of interest |
| CN102766652B (zh) | 2005-08-31 | 2015-07-29 | 孟山都技术有限公司 | 编码杀虫蛋白的核苷酸序列 |
| US7943819B2 (en) | 2005-09-16 | 2011-05-17 | Monsanto Technology Llc | Methods for genetic control of insect infestations in plants and compositions thereof |
| CA2622660C (en) | 2005-09-16 | 2017-11-07 | Devgen Nv | Transgenic plant-based methods for plant pests using rnai |
| JP2009509557A (ja) | 2005-10-05 | 2009-03-12 | バイエル・クロップサイエンス・アーゲー | 改善されたヒアルロン酸産生方法および手段 |
| US20080250533A1 (en) | 2005-10-05 | 2008-10-09 | Claus Frohberg | Plants With an Increased Production of Hyaluronan II |
| JP2009509555A (ja) | 2005-10-05 | 2009-03-12 | バイエル・クロップサイエンス・アーゲー | ヒアルロン酸の産生が増大した植物ｉｉ |
| WO2011066360A1 (en) | 2009-11-24 | 2011-06-03 | Dow Agrosciences Llc | Detection of aad-12 soybean event 416 |
| US20090298787A1 (en) | 2006-01-12 | 2009-12-03 | Devgen N.V. | Dsrna as Insect Control Agent |
| EP1971688B1 (en) | 2006-01-12 | 2012-03-14 | Devgen NV | Dsrna as insect control agent |
| AR056882A1 (es) | 2006-02-01 | 2007-10-31 | Bayer Cropscience Sa | Derivados del fungicida n- cicloalquil- bencil- amida |
| EP1989313B1 (en) | 2006-02-10 | 2016-01-13 | Maharashtra Hybrid Seeds Company Limited (MAHYCO) | Transgenic brinjal (solanum melongena) expressing the cryiac gene |
| US20070214515A1 (en) | 2006-03-09 | 2007-09-13 | E.I.Du Pont De Nemours And Company | Polynucleotide encoding a maize herbicide resistance gene and methods for use |
| PL1999141T3 (pl) | 2006-03-21 | 2011-10-31 | Bayer Cropscience Nv | Nowe geny kodujące białka owadobójcze |
| CA2646476A1 (en) | 2006-03-21 | 2007-09-27 | Bayer Bioscience N.V. | Stress resistant plants |
| UA98770C2 (ru) | 2006-05-26 | 2012-06-25 | Монсанто Текнолоджи, Ллс | Растение кукурузы и семена, которые соответствуют трансгенному случаю mon89034, и способы его обнаружения и применения |
| BRPI0712392B1 (pt) | 2006-06-03 | 2017-09-12 | Syngenta Participations Ag | A nucleic acid moleculum of the mirror maize event, kit and methods for the detection of the same, amplicon, biological sample and extract derived from plants of the reference event, methods for production of a lepidopter pest resistant corn plant understanding the event mir162 and hybrid corn seeds, as well as insecticide protein, nucleic acid molecule, chemical gene, recombinant vector, and procasitic transgenic host cell |
| US7951995B2 (en) | 2006-06-28 | 2011-05-31 | Pioneer Hi-Bred International, Inc. | Soybean event 3560.4.3.5 and compositions and methods for the identification and detection thereof |
| US20080064032A1 (en) | 2006-09-13 | 2008-03-13 | Syngenta Participations Ag | Polynucleotides and uses thereof |
| US7928296B2 (en) | 2006-10-30 | 2011-04-19 | Pioneer Hi-Bred International, Inc. | Maize event DP-098140-6 and compositions and methods for the identification and/or detection thereof |
| US7897846B2 (en) | 2006-10-30 | 2011-03-01 | Pioneer Hi-Bred Int'l, Inc. | Maize event DP-098140-6 and compositions and methods for the identification and/or detection thereof |
| EP2078089B1 (en) | 2006-10-31 | 2016-05-04 | E. I. du Pont de Nemours and Company | Soybean event dp-305423-1 and compositions and methods for the identification and/or detection thereof |
| WO2008114282A2 (en) | 2007-03-19 | 2008-09-25 | Maharashtra Hybrid Seeds Company Limited | Transgenic rice (oryza sativa) comprising pe-7 event and method of detection thereof |
| EP2132320B1 (en) | 2007-04-05 | 2013-08-14 | Bayer CropScience NV | Insect resistant cotton plants and methods for identifying same |
| WO2008150473A2 (en) | 2007-05-30 | 2008-12-11 | Syngenta Participations Ag | Cytochrome p450 genes conferring herbicide resistance |
| US8309818B2 (en) | 2007-06-11 | 2012-11-13 | Bayer Cropscience B.V. | Insect resistant cotton plants and methods for identifying same |
| AU2008281772B2 (en) | 2007-07-31 | 2013-05-30 | Bayer Intellectual Property Gmbh | Fungicidal N-cycloalkyl-benzyl-thiocarboxamides or N-cycloalkyl-benzyl-N' -substituted-amidine derivatives |
| BR122017018105B1 (pt) | 2007-11-15 | 2024-01-23 | Monsanto Technology Llc | Molécula de dna genômico de soja transgênica |
| US9475849B2 (en) | 2007-11-28 | 2016-10-25 | Bayer Cropscience N.V. | Brassica plant comprising a mutant INDEHISCENT allele |
| US8273535B2 (en) | 2008-02-08 | 2012-09-25 | Dow Agrosciences, Llc | Methods for detection of corn event DAS-59132 |
| CN104805115A (zh) | 2008-02-14 | 2015-07-29 | 先锋国际良种公司 | Spt事件侧翼的植物基因组dna及用于鉴定spt事件的方法 |
| EP3260543A1 (en) | 2008-02-15 | 2017-12-27 | Monsanto Technology LLC | Soybean plant and seed corresponding to transgenic event mon87769 and methods for detection thereof |
| BRPI0908267B8 (pt) | 2008-02-29 | 2019-02-05 | Monsanto Technology Llc | método de produção de uma planta de milho tolerante a seca |
| CA2950653C (en) | 2008-04-14 | 2021-01-05 | Bayer Cropscience Nv | New mutated hydroxyphenylpyruvate dioxygenase, dna sequence and isolation of plants which are tolerant to hppd inhibitor herbicides |
| WO2009140769A1 (en) | 2008-05-22 | 2009-11-26 | Merck Frosst Canada Ltd. | 3, 4 - substituted piperidine derivatives as renin inhibitors |
| EP2143797A1 (de) | 2008-07-10 | 2010-01-13 | Bayer CropScience AG | Weizenstärke sowie Weizenmehle und Lebensmittel enthaltend diese Weizenstärke/Weizenmehle |
| EA029333B1 (ru) | 2008-07-17 | 2018-03-30 | Байер Кропсайенс Н.В. | Растение brassica, содержащее мутантный аллель indehiscent |
| BRPI0911744A2 (pt) | 2008-08-01 | 2015-08-18 | Bayer Bioscience Nv | "método para aumentar a produção de biomassa e/ou a produção de sementes e/ou a fixação de carbono em plantas de arroz, planta de arroz, transgênico, semente de arroz, grão de arroz, farinha e produto alimentício" |
| WO2010024976A1 (en) | 2008-08-29 | 2010-03-04 | Monsanto Technology Llc | Soybean plant and seed corresponding to transgenic event mon87754 and methods for detection thereof |
| BRPI0920827A2 (pt) | 2008-09-29 | 2015-08-18 | Monsanto Technology Llc | Evento transgênico da soja mon87705 e métodos para detecção do mesmo |
| MX346319B (es) | 2008-12-16 | 2017-03-15 | Syngenta Participations Ag | Evento 5307 del maiz. |
| UA106061C2 (uk) | 2008-12-19 | 2014-07-25 | Сінгента Партісіпейшнс Аг | Трансгенний варіант цукрового буряку gm rz13 |
| MX355477B (es) | 2009-01-07 | 2018-04-19 | Basf Agrochemical Products Bv | Soja de evento 127 y metodos relacionados con la misma. |
| AR075573A1 (es) * | 2009-02-11 | 2011-04-20 | Basf Se | Dimethomorph como protector de plaguicidas con efectos fitotoxicos |
| JP5762400B2 (ja) | 2009-03-30 | 2015-08-12 | モンサント テクノロジー エルエルシー | イネ遺伝子組換え事象１７０５３およびその使用方法 |
| JP5769698B2 (ja) | 2009-03-30 | 2015-08-26 | モンサント テクノロジー エルエルシー | 遺伝子組換えイネ事象１７３１４およびその使用方法 |
| CA2759276A1 (en) | 2009-04-22 | 2010-10-28 | Bayer Bioscience N.V. | Production of multi-antennary n-glycan structures in plants |
| EP2251331A1 (en) | 2009-05-15 | 2010-11-17 | Bayer CropScience AG | Fungicide pyrazole carboxamides derivatives |
| AR076839A1 (es) * | 2009-05-15 | 2011-07-13 | Bayer Cropscience Ag | Derivados fungicidas de pirazol carboxamidas |
| CA2765287C (en) | 2009-06-15 | 2018-12-11 | Bayer Bioscience N.V. | Nicotiana benthamiana plants deficient in xylosyltransferase activity |
| EP2449108A1 (en) | 2009-07-01 | 2012-05-09 | Bayer BioScience N.V. | Methods and means for obtaining plants with enhanced glyphosate tolerance |
| MX2012000202A (es) | 2009-07-02 | 2012-02-28 | Athenix Corp | Gen plaguicida axmi-205 y metodos para su uso. |
| EA035563B1 (ru) | 2009-07-31 | 2020-07-08 | Басф Агрикалчерал Солюшнс Сид Юс Ллк | Молекула рекомбинантной нуклеиновой кислоты, кодирующей полипептид с пестицидной активностью против чешуекрылых, жесткокрылых или нематодных вредителей, ее получение и применение |
| AU2010284284B2 (en) | 2009-08-19 | 2015-09-17 | Corteva Agriscience Llc | AAD-1 event DAS-40278-9, related transgenic corn lines, and event-specific identification thereof |
| CN102596984A (zh) | 2009-09-17 | 2012-07-18 | 孟山都技术公司 | 大豆转基因事件mon 87708及其使用方法 |
| PL2501804T3 (pl) | 2009-11-20 | 2016-11-30 | Rośliny Brassica zawierające zmutowane allele FAD3 | |
| MX358629B (es) | 2009-11-23 | 2018-08-28 | Monsanto Technology Llc | Evento transgenico de maiz mon 87427 y la escala de desarrollo relativo. |
| NZ600375A (en) | 2009-11-23 | 2014-10-31 | Bayer Cropscience Nv | Herbicide tolerant soybean plants and methods for identifying same |
| CN102711444B (zh) | 2009-11-24 | 2015-08-12 | 陶氏益农公司 | Aad-12事件416、相关的转基因大豆系及其事件特异性鉴定 |
| US8581046B2 (en) | 2010-11-24 | 2013-11-12 | Pioneer Hi-Bred International, Inc. | Brassica gat event DP-073496-4 and compositions and methods for the identification and/or detection thereof |
| WO2011084632A1 (en) | 2009-12-17 | 2011-07-14 | Pioneer Hi-Bred International, Inc. | Maize event dp-032316-8 and methods for detection thereof |
| HUE045002T2 (hu) | 2009-12-17 | 2019-11-28 | Pioneer Hi Bred Int | DP-004114-3 kukoricaesemény és ennek detektálási módszerei |
| US20110154525A1 (en) | 2009-12-17 | 2011-06-23 | Pioneer Hi-Bred International, Inc. | Maize event DP-040416-8 and methods for detection thereof |
| WO2011075595A1 (en) | 2009-12-17 | 2011-06-23 | Pioneer Hi-Bred International, Inc. | Maize event dp-043a47-3 and methods for detection thereof |
| US20120255051A1 (en) | 2009-12-22 | 2012-10-04 | Rene Ruiter | Herbicide tolerant plants |
| MX2012007360A (es) | 2009-12-23 | 2012-11-06 | Bayer Ip Gmbh | Plantas tolerantes a herbicidas inhibidores de las hppd. |
| EA201290559A1 (ru) | 2009-12-23 | 2013-01-30 | Байер Интеллектуэль Проперти Гмбх | Растения, устойчивые к гербицидам - ингибиторам hppd |
| MX2012007358A (es) | 2009-12-23 | 2012-11-06 | Bayer Ip Gmbh | Plantas tolerantes a herbicidas inhibidores de las hppd. |
| UY33139A (es) | 2009-12-23 | 2011-07-29 | Bayer Cropscience Ag | Plantas tolerantes a herbicidas inhibidores de las hppd |
| EP2516635B1 (en) | 2009-12-23 | 2017-11-15 | Bayer Intellectual Property GmbH | Plants tolerant to hppd inhibitor herbicides |
| EP2529019B1 (en) | 2010-01-25 | 2014-10-01 | Bayer CropScience NV | Methods for manufacturing plant cell walls comprising chitin |
| CA2788238C (en) | 2010-02-04 | 2019-09-03 | Fritz Kreuzaler | A method for increasing photosynthetic carbon fixation using glycolate dehydrogenase multi-subunit fusion protein |
| BR112012020921A2 (pt) | 2010-02-18 | 2015-09-08 | Athenix Corp | genes de delta-endotoxina axmi218, axmi219, axmi220, axmi226, axmi227, axmi228, axmi229, axmi230 e axmi231 e métodos para sua utilização |
| HUE035576T2 (en) | 2010-02-18 | 2018-05-28 | Athenix Corp | AXMI221Z, AXMI222Z, AXMI223Z, AXMI224Z, and AXMI225Z delta-endotoxin genes and methods of their application |
| US20110218107A1 (en) | 2010-03-02 | 2011-09-08 | Bayer Cropscience Ag | Use of Propineb for Physiological Curative Treatment Under Zinc Deficiency |
| KR101941297B1 (ko) | 2010-06-04 | 2019-01-22 | 몬산토 테크놀로지 엘엘씨 | 유전자 이식 브라씨카의 사건 mon 88302 및 이것의 사용방법 |
| BR112013005431A2 (pt) | 2010-09-08 | 2016-06-07 | Dow Agrosciences Llc | "evento 1606 de aad-12 e linhagens de soja transgênica relacionadas". |
| KR20130119438A (ko) | 2010-10-12 | 2013-10-31 | 몬산토 테크놀로지 엘엘씨 | 유전자도입 이벤트 mon87712에 상응하는 대두 식물과 종자, 그리고 이들의 검출을 위한 방법 |
| BR112013010278B1 (pt) | 2010-10-27 | 2020-12-29 | Ceres, Inc | método para produzir uma planta, método para modular a composição de biomassa em uma planta, ácido nucleico isolado e método para alterar a composição de biomassa em uma planta |
| WO2012071039A1 (en) | 2010-11-24 | 2012-05-31 | Pioner Hi-Bred International, Inc. | Brassica gat event dp-061061-7 and compositions and methods for the identification and/or detection thereof |
| WO2012075426A1 (en) | 2010-12-03 | 2012-06-07 | Dow Agrosciences Llc | Stacked herbicide tolerance event 8264.44.06.1, related transgenic soybean lines, and detection thereof |
| CA2820706C (en) | 2010-12-03 | 2018-05-22 | Ms Technologies, Llc | Optimized expression of glyphosate resistance encoding nucleic acid molecules in plant cells |
| WO2012075429A1 (en) | 2010-12-03 | 2012-06-07 | Dow Agrosciences Llc | Stacked herbicide tolerance event 8291.45.36.2, related transgenic soybean lines, and detection thereof |
| TWI667347B (zh) | 2010-12-15 | 2019-08-01 | 瑞士商先正達合夥公司 | 大豆品種ｓｙｈｔ０ｈ２及偵測其之組合物及方法 |
| CN103282377B (zh) | 2010-12-28 | 2015-03-04 | 丰田自动车株式会社 | 成熟叶特异性启动子 |
| HUE026725T2 (en) * | 2011-04-22 | 2016-06-28 | Bayer Ip Gmbh | Active compositions comprising a fungicidal carboxamide derivative and an insecticidal or acaricidal or nematicidal active compound |
| ES2714714T3 (es) * | 2011-04-22 | 2019-05-29 | Bayer Cropscience Ag | Composiciones de compuestos activos que comprenden un derivado de (tio)carboximida y un compuesto fungicida |
| KR102123218B1 (ko) | 2012-10-19 | 2020-06-16 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 카르복사미드 유도체 및 생물학적 제어제를 포함하는 활성 화합물 조합물 |
| CN105357967B (zh) | 2012-10-19 | 2019-02-19 | 拜尔农科股份公司 | 使用羧酰胺衍生物促进植物生长的方法 |
| KR102134565B1 (ko) | 2012-10-19 | 2020-07-16 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 카르복사미드 또는 티오카르복사미드 유도체를 사용한 살진균제에 내성을 가지는 진균에 대항하는 식물의 처리 방법 |
| EA025862B1 (ru) | 2012-10-19 | 2017-02-28 | Байер Кропсайенс Аг | Способ повышения устойчивости к абиотическому стрессу в растениях с использованием производных карбоксамида или тиокарбоксамида |
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2013
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- 2013-10-17 EP EP13777076.4A patent/EP2908639A1/en not_active Withdrawn
- 2013-10-17 CA CA2888600A patent/CA2888600C/en active Active
- 2013-10-17 CN CN201380054677.7A patent/CN105357968A/zh active Pending
- 2013-10-17 UA UAA201504671A patent/UA114822C2/uk unknown
- 2013-10-17 WO PCT/EP2013/071694 patent/WO2014060502A1/en not_active Ceased
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| CN105357968A (zh) | 2016-02-24 |
| EP2908639A1 (en) | 2015-08-26 |
| EA201590771A1 (ru) | 2015-08-31 |
| AR093069A1 (es) | 2015-05-13 |
| WO2014060502A1 (en) | 2014-04-24 |
| AU2017213448A1 (en) | 2017-08-24 |
| AU2013333916B2 (en) | 2017-05-25 |
| EA026839B1 (ru) | 2017-05-31 |
| AU2017213448B2 (en) | 2018-10-04 |
| US9801374B2 (en) | 2017-10-31 |
| JP6153619B2 (ja) | 2017-06-28 |
| UA114822C2 (uk) | 2017-08-10 |
| CA2888600A1 (en) | 2014-04-24 |
| JP2015536313A (ja) | 2015-12-21 |
| AU2013333916A1 (en) | 2015-06-04 |
| US20150245610A1 (en) | 2015-09-03 |
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