EA026839B1 - Комбинации активных соединений, содержащие карбоксамидные соединения - Google Patents
Комбинации активных соединений, содержащие карбоксамидные соединения Download PDFInfo
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- EA026839B1 EA026839B1 EA201590771A EA201590771A EA026839B1 EA 026839 B1 EA026839 B1 EA 026839B1 EA 201590771 A EA201590771 A EA 201590771A EA 201590771 A EA201590771 A EA 201590771A EA 026839 B1 EA026839 B1 EA 026839B1
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- plants
- fluoro
- methyl
- cyclopropyl
- compound
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- MBMQEIFVQACCCH-UHFFFAOYSA-N trans-Zearalenon Natural products O=C1OC(C)CCCC(=O)CCCC=CC2=CC(O)=CC(O)=C21 MBMQEIFVQACCCH-UHFFFAOYSA-N 0.000 description 1
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- LINOMUASTDIRTM-UHFFFAOYSA-N vomitoxin hydrate Natural products OCC12C(O)C(=O)C(C)=CC1OC1C(O)CC2(C)C11CO1 LINOMUASTDIRTM-UHFFFAOYSA-N 0.000 description 1
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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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12356025 | 2012-10-19 | ||
| US201261730251P | 2012-11-27 | 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 |
|---|---|
| EA201590771A1 EA201590771A1 (ru) | 2015-08-31 |
| EA026839B1 true EA026839B1 (ru) | 2017-05-31 |
Family
ID=47216180
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201590771A EA026839B1 (ru) | 2012-10-19 | 2013-10-17 | Комбинации активных соединений, содержащие карбоксамидные соединения |
Country Status (10)
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| EP (1) | EP2908639A1 (enExample) |
| JP (1) | JP6153619B2 (enExample) |
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| AR (1) | AR093069A1 (enExample) |
| AU (2) | AU2013333916B2 (enExample) |
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| EA (1) | EA026839B1 (enExample) |
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Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA114528C2 (uk) | 2012-10-19 | 2017-06-26 | Байєр Кропсайнс Аг | Комбінації активних сполук, що містять карбоксамідні похідні та засіб біологічної боротьби |
| AU2013333847B2 (en) | 2012-10-19 | 2017-04-20 | Bayer Cropscience Ag | Method for treating plants against fungi resistant to fungicides using carboxamide or thiocarboxamide derivatives |
| AU2013333845B2 (en) * | 2012-10-19 | 2017-06-08 | Bayer Cropscience Ag | Method of plant growth promotion using carboxamide derivatives |
| MX381528B (es) * | 2012-10-19 | 2025-03-12 | Bayer Cropscience Ag | Método para mejorar la tolerancia al estrés abiótico en plantas usando derivados de carboxamida o tiocarboxamida. |
| 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 |
| US20190307127A1 (en) | 2016-10-10 | 2019-10-10 | Basf Se | Pesticidal Mixtures |
| WO2018069109A1 (en) | 2016-10-10 | 2018-04-19 | Basf Se | Pesticidal mixtures |
| WO2018069110A1 (en) | 2016-10-10 | 2018-04-19 | 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 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010092119A1 (en) * | 2009-02-11 | 2010-08-19 | Basf Se | Dimethomorph as safener for pesticides with phytotoxic effects |
| EP2251331A1 (en) * | 2009-05-15 | 2010-11-17 | Bayer CropScience AG | Fungicide pyrazole carboxamides derivatives |
| WO2010130767A2 (en) * | 2009-05-15 | 2010-11-18 | Bayer Cropscience Ag | Fungicide pyrazole carboxamides derivatives |
| WO2011107443A1 (en) * | 2010-03-02 | 2011-09-09 | Bayer Cropscience Ag | Use of propineb for physiological curative treatment under zinc deficiency |
| WO2012143127A1 (en) * | 2011-04-22 | 2012-10-26 | Bayer Cropsciences Ag | Active compound combinations comprising a (thio)carboxamide derivative and a fungicidal compound |
| WO2012143125A1 (en) * | 2011-04-22 | 2012-10-26 | Bayer Cropscience Ag | Active compound combinations comprising a (thio)carboxamide derivative and an insecticidal or acaricidal or nematicidal active compound |
Family Cites Families (330)
| 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 |
| WO1979000427A1 (en) | 1977-12-23 | 1979-07-12 | Ici Ltd | Herbicidal pyridine derivative |
| EP0003114B1 (de) | 1978-01-18 | 1982-01-27 | Ciba-Geigy Ag | Herbizid wirksame ungesättigte Ester von 4-(3',5'-Dihalogenpyridyl -(2')-oxy)-alpha-phenoxypropionsäuren, Verfahren zu ihrer Herstellung sowie sie enthaltende herbizide Mittel und deren Verwendung |
| EP0003890B2 (en) | 1978-03-01 | 1990-04-04 | Imperial Chemical Industries 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 |
| DK456982A (da) | 1981-10-16 | 1983-04-17 | Du Pont | Phenyl-substituerede sulfonamider |
| MA19709A1 (fr) | 1982-02-17 | 1983-10-01 | Ciba Geigy Ag | Application de derives de quinoleine a la protection des plantes cultivees . |
| ATE103902T1 (de) | 1982-05-07 | 1994-04-15 | Ciba Geigy Ag | Verwendung von chinolinderivaten zum schuetzen 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 |
| ES2018274T5 (es) | 1986-03-11 | 1996-12-16 | Plant Genetic Systems Nv | Celulas vegetales resistentes a los inhibidores de glutamina sintetasa, preparadas por ingenieria genetica. |
| EP0249707B1 (en) | 1986-06-14 | 1992-03-11 | Kumiai 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| ES2058314T3 (es) | 1988-01-06 | 1994-11-01 | Uniroyal Chem Co Inc | Herbicidas de quinoxaliniloxifenoxipropanoato de heterociclo-alquileno. |
| 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 |
| EP0412911B1 (en) | 1989-08-10 | 2001-07-18 | Aventis CropScience N.V. | Plants 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 |
| WO1991013548A1 (en) | 1990-03-14 | 1991-09-19 | Ahle James L | Herbicidal compositions of aroylated 1,3-dicarbonyl or 1,3,5-tricarbonyl cyclohexane herbicides and an antidote system therefor |
| DK0476093T3 (da) | 1990-04-04 | 1997-06-02 | Pioneer Hi Bred Int | Fremstilling af forbedret rapsfrø, der udviser et reduceret indhold af mættet fedtsyre |
| US5198599A (en) | 1990-06-05 | 1993-03-30 | Idaho Resarch Foundation, Inc. | Sulfonylurea herbicide resistance in plants |
| WO1992000377A1 (en) | 1990-06-25 | 1992-01-09 | Monsanto Company | Glyphosate tolerant plants |
| 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 (enExample) | 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 |
| EP0664835B1 (en) | 1992-10-14 | 2004-05-19 | Syngenta 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 |
| EP1471145A2 (en) | 1993-03-25 | 2004-10-27 | Syngenta Participations AG | Pesticipal proteins and strains |
| 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 |
| CA2150667C (en) | 1993-10-01 | 2007-01-09 | Mari Iwabuchi | A gene which determines cytoplasmic sterility and a method of producing hybrid plants using said gene |
| AU692791B2 (en) | 1993-10-12 | 1998-06-18 | Agrigenetics, Inc. | Brassica napus variety AG019 |
| EP0728213B2 (en) | 1993-11-09 | 2008-12-10 | E.I. Du Pont De Nemours And Company | Transgenic fructan accumulating crops and methods for their production |
| AU688006B2 (en) | 1994-03-25 | 1998-03-05 | Brunob Ii B.V. | Method for producing altered starch from potato plants |
| RU2201963C2 (ru) | 1994-05-18 | 2003-04-10 | Плант Тек Биотехнологи Гмбх Форшунг Унд Энтвиклунг | ПОСЛЕДОВАТЕЛЬНОСТЬ ДНК (ВАРИАНТЫ), РЕКОМБИНАНТНАЯ ДНК, ПРОТЕИН, СПОСОБ ПОЛУЧЕНИЯ ПРОТЕИНА, СПОСОБ ПОЛУЧЕНИЯ МИКРООРГАНИЗМОВ, СПОСОБ ПОЛУЧЕНИЯ КЛЕТОК ГРИБА, СПОСОБ ПОЛУЧЕНИЯ ЛИНЕЙНЫХ α-1,4-ГЛЮКАНОВ И/ИЛИ ФРУКТОЗЫ И СПОСОБ ПОЛУЧЕНИЯ ЛИНЕЙНЫХ α-1,4-ГЛЮКАНОВ И/ИЛИ ФРУКТОЗЫ IN VITRO |
| US5824790A (en) | 1994-06-21 | 1998-10-20 | Zeneca Limited | Modification of starch synthesis in plants |
| AU706849B2 (en) | 1994-06-21 | 1999-06-24 | Cerestar Usa, Inc. | Novel plants and processes for obtaining them |
| 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 |
| AU710172B2 (en) | 1995-02-24 | 1999-09-16 | Basf Aktiengesellschaft | Pyrazolylbenzoyl derivatives |
| 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 |
| US6825342B1 (en) | 1995-05-05 | 2004-11-30 | National Starch And Chemical Investment Holding Corporation | Plant starch composition |
| 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 |
| US5712107A (en) | 1995-06-07 | 1998-01-27 | Pioneer Hi-Bred International, Inc. | Substitutes for modified starch and latexes in paper manufacture |
| US6284479B1 (en) | 1995-06-07 | 2001-09-04 | 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 |
| DE59611362D1 (de) | 1995-09-19 | 2006-08-17 | Bayer Bioscience Gmbh | Pflanzen, die eine modifizierte stärke synthetisieren, verfahren zu ihrer herstellung sowie modifizierte stärke |
| 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 |
| CN1257978C (zh) | 1996-05-29 | 2006-05-31 | 赫彻斯特-舍林农业发展有限公司 | 编码小麦中参与淀粉合成的酶的核酸分子 |
| JP2000512348A (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 |
| ATE211198T1 (de) | 1996-06-12 | 2002-01-15 | Pioneer Hi Bred Int | Ersatzmaterial für modifizierte stärke in der papierherstellung |
| WO1997047806A1 (en) | 1996-06-12 | 1997-12-18 | Pioneer Hi-Bred International, Inc. | Substitutes for modified starch in paper manufacture |
| 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 |
| WO1998044140A1 (en) | 1997-04-03 | 1998-10-08 | Dekalb Genetics Corporation | 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 |
| DE19820607A1 (de) | 1998-05-08 | 1999-11-11 | Hoechst Schering Agrevo Gmbh | Nucleinsäuremoleküle codierend Enzyme aus Weizen, die an der Stärkesynthese beteiligt sind |
| DE19820608A1 (de) | 1998-05-08 | 1999-11-11 | Hoechst Schering Agrevo Gmbh | Nucleinsäuremoleküle codierend Enzyme aus Weizen, die an der Stärkesynthese beteiligt sind |
| PT1852424E (pt) | 1998-05-11 | 2012-05-07 | Basf Se | Processo para a preparação de isoxazolino-3-ilacilbenzenos |
| WO1999058654A2 (de) | 1998-05-13 | 1999-11-18 | Planttec Biotechnologie Gmbh Forschung & Entwicklung | 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 |
| WO1999066050A1 (en) | 1998-06-15 | 1999-12-23 | National Starch And Chemical Investment Holding Corporation | Improvements in or relating to plants and plant products |
| 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 |
| 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 |
| 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 |
| WO2000011192A2 (en) | 1998-08-25 | 2000-03-02 | Pioneer Hi-Bred International, Inc. | Plant glutamine: fructose-6-phosphate amidotransferase nucleic acids |
| AU9535798A (en) | 1998-09-02 | 2000-03-27 | Planttec Biotechnologie Gmbh | Nucleic acid molecules encoding an amylosucrase |
| DK1117802T3 (da) | 1998-10-09 | 2010-05-25 | Bayer Bioscience Gmbh | Nukleinsyremolekyler, der koder for et forgreningsenzym fra bakterier af slægten Neisseria samt fremgangsmåde til fremstilling af alfa-1,6-forgrenede alfa-1,4-glucaner |
| DE19924342A1 (de) | 1999-05-27 | 2000-11-30 | Planttec Biotechnologie Gmbh | Genetisch modifizierte Pflanzenzellen und Pflanzen mit erhöhter Aktivität eines Amylosucraseproteins und eines Verzweigungsenzyms |
| US6333449B1 (en) | 1998-11-03 | 2001-12-25 | Plant Genetic Systems, N.V. | Glufosinate tolerant rice |
| AU1336200A (en) | 1998-11-03 | 2000-05-22 | Aventis Cropscience 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 |
| CA2365590A1 (en) | 1999-04-29 | 2000-11-09 | Zeneca Limited | Herbicide resistant plants |
| WO2000066747A1 (en) | 1999-04-29 | 2000-11-09 | Syngenta Limited | Herbicide resistant plants |
| 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 |
| DE60111613T2 (de) | 2000-03-09 | 2006-05-18 | Monsanto Technology Llc. | Verfahren zum herstellen von glyphosat-toleranten pflanzen |
| US6822146B2 (en) | 2000-03-09 | 2004-11-23 | E. I. Du Pont De Nemours And Company | Sulfonylurea-tolerant sunflower line M7 |
| AU8729901A (en) | 2000-03-31 | 2001-10-15 | Aventis Cropscience Gmbh | Benzoylpyrazols 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 | |
| BR122013026754B1 (pt) | 2000-06-22 | 2018-02-27 | Monsanto Company | Molécula de dna e processos para produzir uma planta de milho tolerante à aplicação do herbicida glifosato |
| AU2001295504A1 (en) | 2000-08-25 | 2002-03-04 | Basf Aktiengesellschaft | A herbicidal synergistic combination of a dihydrobenzothiophene compound 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 |
| WO2002026995A1 (en) | 2000-09-29 | 2002-04-04 | Syngenta Limited | Herbicide resistant plants |
| 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 |
| WO2002034946A2 (en) | 2000-10-25 | 2002-05-02 | Monsanto Technology Llc | Cotton event pv-ghgt07(1445) and compositions and methods for detection thereof |
| WO2005012515A2 (en) | 2003-04-29 | 2005-02-10 | Pioneer Hi-Bred International, Inc. | Novel glyphosate-n-acetyltransferase (gat) genes |
| US7306909B2 (en) | 2000-10-30 | 2007-12-11 | Monsanto Technology Llc | Canola event pv-bngt04(rt73) and compositions and methods for detection thereof |
| CA2425956C (en) | 2000-10-30 | 2014-12-23 | Maxygen, Inc. | Novel glyphosate n-acetyltransferase (gat) genes |
| 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 |
| EP1341903B1 (en) | 2000-12-07 | 2012-12-26 | Syngenta Limited | Plant derived hydroxy phenyl pyruvate dioxygneases (hppd) resistant against triketone herbicides and transgenic plants containing these dioxygenases |
| EP1349446B1 (en) | 2000-12-08 | 2013-01-23 | Commonwealth Scientific And Industrial Research Organisation | Modification of sucrose synthase gene expression in plant tissue and uses therefor |
| 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 |
| AU2002338233A1 (en) | 2001-03-30 | 2002-10-15 | 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 |
| PT1483390E (pt) | 2001-06-12 | 2008-07-07 | Bayer Cropscience Ag | Plantas transgénicas que sintetizam amido rico em amilose |
| US6818807B2 (en) | 2001-08-06 | 2004-11-16 | Bayer Bioscience N.V. | Herbicide tolerant cotton plants having event EE-GH1 |
| US20030084473A1 (en) | 2001-08-09 | 2003-05-01 | Valigen | Non-transgenic herbicide resistant plants |
| BRPI0213423A2 (pt) | 2001-10-17 | 2017-05-02 | Basf Plant Science Gmbh | amido e método para produção do mesmo |
| AR037856A1 (es) | 2001-12-17 | 2004-12-09 | Syngenta Participations Ag | Evento de maiz |
| 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 |
| US7705216B2 (en) | 2002-07-29 | 2010-04-27 | 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 |
| GB0225129D0 (en) | 2002-10-29 | 2002-12-11 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
| EP1558767A2 (en) | 2002-10-29 | 2005-08-03 | BASF Plant Science GmbH | Compositions and methods for identifying plants having increased tolerance to imidazolinone herbicides |
| US20040110443A1 (en) | 2002-12-05 | 2004-06-10 | Pelham Matthew C. | Abrasive webs and methods of making the same |
| WO2004053062A2 (en) | 2002-12-05 | 2004-06-24 | Monsanto Technology Llc | Bentgrass event asr-368 and compositions and methods for detection thereof |
| PT1578973E (pt) | 2002-12-19 | 2008-10-16 | Bayer Cropscience Ag | Células de plantas e plantas que sintetizam um amido com uma melhor viscosidade final |
| AU2004211592B2 (en) | 2003-02-12 | 2008-04-10 | Monsanto Technology Llc | Cotton event MON 88913 and compositions and methods for detection thereof |
| US7335816B2 (en) | 2003-02-28 | 2008-02-26 | Kws Saat Ag | Glyphosate tolerant sugar beet |
| CA2502981C (en) | 2003-02-20 | 2012-09-11 | Kws Saat Ag | Transgenic glyphosate tolerant sugar beet event h7-1 |
| CN1777677A (zh) | 2003-03-07 | 2006-05-24 | 巴斯福植物科学有限公司 | 增强植物中直链淀粉产量 |
| JP4960699B2 (ja) | 2003-04-09 | 2012-06-27 | バイエル・バイオサイエンス・エヌ・ヴェー | ストレス条件に対する植物の耐性を増加させるための方法及び手段 |
| MXPA05011795A (es) | 2003-05-02 | 2006-02-17 | Dow Agrosciences Llc | Evidencia de maiz tc1507 y metodos para deteccion del mismo. |
| WO2005002359A2 (en) | 2003-05-22 | 2005-01-13 | Syngenta Participations Ag | Modified starch, uses, methods for production thereof |
| CA2527115C (en) | 2003-05-28 | 2019-08-13 | Basf Aktiengesellschaft | 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 |
| ES2354696T3 (es) | 2003-07-31 | 2011-03-17 | Toyo Boseki Kabushiki Kaisha | Planta que produce ácido hialurónico. |
| CN100575490C (zh) | 2003-08-15 | 2009-12-30 | 联邦科学与工业研究组织 | 改变产纤维植物中纤维特征的方法和手段 |
| ES2743420T3 (es) | 2003-08-29 | 2020-02-19 | Instituto Nac De Tecnologia Agropecuaria | Plantas de arroz que tienen tolerancia incrementada frente a herbicidas de imidazolinona |
| EP1687417B9 (en) | 2003-09-30 | 2011-03-30 | Bayer CropScience AG | Plants with reduced activity of a class 3 branching enzyme |
| WO2005030941A1 (en) | 2003-09-30 | 2005-04-07 | Bayer Cropscience Gmbh | Plants with increased activity of a class 3 branching enzyme |
| WO2005054480A2 (en) | 2003-12-01 | 2005-06-16 | Syngenta Participations Ag | Insect resistant cotton plants and methods of detecting the same |
| BRPI0416472A (pt) | 2003-12-01 | 2007-03-06 | Syngenta Participations Ag | plantas de algodão resistentes a insetos e métodos de detecção das mesmas |
| US7157281B2 (en) | 2003-12-11 | 2007-01-02 | Monsanto Technology Llc | High lysine maize compositions and event LY038 maize plants |
| HRP20150814T1 (xx) | 2003-12-15 | 2015-08-28 | Monsanto Technology, Llc | Biljka kukuruza mon88017 te sastavi i postupci za njezino otkrivanje |
| EP1725666B1 (en) | 2004-03-05 | 2012-01-11 | Bayer CropScience AG | Plants with reduced activity of the starch phosphorylating enzyme phosphoglucan, water 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 |
| AR048026A1 (es) | 2004-03-05 | 2006-03-22 | Bayer Cropscience Gmbh | Procedimientos para la identificacion de proteinas con actividad enzimatica fosforiladora de almidon |
| US7432082B2 (en) | 2004-03-22 | 2008-10-07 | Basf Ag | Methods and compositions for analyzing AHASL genes |
| CA2559481C (en) | 2004-03-25 | 2014-04-08 | Henry-York Steiner | Corn event mir604 |
| AU2004318788B2 (en) | 2004-03-26 | 2011-12-22 | Corteva Agriscience Llc | Cry1F and Cry1Ac transgenic cotton lines and event-specific identification thereof |
| EP1766030A2 (en) | 2004-06-16 | 2007-03-28 | 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 |
| EP1776457A1 (en) | 2004-07-30 | 2007-04-25 | BASF Agrochemical Products, B.V. | Herbicide-resistant sunflower plants, polynucleotides encoding herbicide-resistant acetohydroxy acid synthase large subunit proteins, and methods of use |
| CN101035900A (zh) | 2004-08-04 | 2007-09-12 | 巴斯福植物科学有限公司 | 单子叶植物ahass序列和使用方法 |
| DK1786908T3 (da) | 2004-08-18 | 2010-06-07 | Bayer Cropscience Ag | Planter med forøget plastidisk aktivitet af stivelsesphosphorylerende R3-enzym |
| 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 |
| CA2588243C (en) | 2004-09-29 | 2013-06-11 | Pioneer Hi-Bred International, Inc. | Corn event das-59122-7 and methods for detection thereof |
| CN101090971B (zh) | 2004-10-29 | 2013-01-02 | 拜尔作物科学公司 | 耐受胁迫的棉花植物 |
| 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 |
| PT1868426T (pt) | 2005-03-16 | 2018-05-08 | Syngenta Participations Ag | Evento de milho 3272 e métodos para a sua deteção |
| 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 |
| EP1710315A1 (de) | 2005-04-08 | 2006-10-11 | Bayer CropScience GmbH | Hoch Phosphat Stärke |
| CN101151373B (zh) | 2005-04-08 | 2016-02-24 | 拜尔作物科学公司 | 原种事件a2704-12以及用于鉴定生物样品中此事件的方法和试剂盒 |
| PT1871901E (pt) | 2005-04-11 | 2011-09-29 | Bayer Bioscience Nv | Acontecimento elite a5547-127 e processos e kits para identificar um tal acontecimento em amostras biológicas |
| 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 |
| EP1917359A2 (en) | 2005-06-02 | 2008-05-07 | Syngeta Participations AG | Ce43-67b, insecticidal transgenic cotton expressing cry1ab |
| WO2006128569A2 (en) | 2005-06-02 | 2006-12-07 | Syngenta Participations Ag | 1143-14a, insecticidal transgenic cotton expressing cry1ab |
| WO2006128568A2 (en) | 2005-06-02 | 2006-12-07 | Syngenta Participations Ag | T342-142, insecticidal transgenic cotton expressing cry1ab |
| WO2006128570A1 (en) | 2005-06-02 | 2006-12-07 | Syngenta Participations Ag | 1143-51b insecticidal cotton |
| WO2006128572A1 (en) | 2005-06-02 | 2006-12-07 | Syngenta Participations Ag | Ce46-02a insecticidal cotton |
| WO2006131230A2 (de) | 2005-06-09 | 2006-12-14 | Bayer Cropscience Ag | Wirkstoffkombinationen |
| MX2007016199A (es) | 2005-06-15 | 2008-03-11 | Bayer Bioscience Nv | Metodos para aumentar la resistencia de plantas a condiciones hipoxicas. |
| KR101409553B1 (ko) | 2005-06-24 | 2014-06-20 | 바이엘 크롭사이언스 엔.브이. | 식물 세포벽의 반응성을 변경하는 방법 |
| 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. |
| AU2006283504B2 (en) | 2005-08-24 | 2011-08-25 | E. I. Du Pont De Nemours And Company | Compositions providing tolerance to multiple herbicides and methods of use thereof |
| WO2007027777A2 (en) | 2005-08-31 | 2007-03-08 | Monsanto Technology Llc | Nucleotide sequences encoding insecticidal proteins |
| ES2557512T3 (es) | 2005-09-16 | 2016-01-26 | Devgen N.V. | Métodos basados en plantas transgénicas para plagas de plantas usando ARNi |
| CN102409050A (zh) | 2005-09-16 | 2012-04-11 | 孟山都技术有限公司 | 用于在植物中遗传控制昆虫侵袭的方法和组合物 |
| CA2624496A1 (en) | 2005-10-05 | 2007-04-12 | Bayer Cropscience Ag | 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 |
| US8106256B2 (en) | 2005-10-05 | 2012-01-31 | Bayer Cropscience Ag | Methods and means for producing hyaluronan |
| WO2011066360A1 (en) | 2009-11-24 | 2011-06-03 | Dow Agrosciences Llc | Detection of aad-12 soybean event 416 |
| JP5474355B2 (ja) | 2006-01-12 | 2014-04-16 | デブジェン エヌブイ | RNAiを利用する植物害虫のための遺伝子組換え植物系方法 |
| EP2374462A3 (en) | 2006-01-12 | 2011-12-14 | deVGen N.V. | Methods for controlling pests using RNAi |
| AR056882A1 (es) | 2006-02-01 | 2007-10-31 | Bayer Cropscience Sa | Derivados del fungicida n- cicloalquil- bencil- amida |
| TR200805941T2 (tr) | 2006-02-10 | 2009-02-23 | Maharashtra Hybrid Seeds Company Limited (Mahyco) | Transgenik brinjal (solanum melongena) içeren EE-1 olgusu |
| 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 |
| US8158856B2 (en) | 2006-03-21 | 2012-04-17 | Bayer Cropscience Nv | Stress resistant plants |
| EP1999141B1 (en) | 2006-03-21 | 2011-06-01 | Bayer BioScience N.V. | Novel genes encoding insecticidal proteins |
| JP5513883B2 (ja) | 2006-05-26 | 2014-06-04 | モンサント テクノロジー エルエルシー | トランスジェニック事象mon89034に対応するトウモロコシ植物および種子ならびにそれらを検出および使用するための方法 |
| KR101327245B1 (ko) | 2006-06-03 | 2013-11-12 | 신젠타 파티서페이션즈 아게 | 옥수수 이벤트 mir162 |
| 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 |
| ES2582552T3 (es) | 2006-10-31 | 2016-09-13 | E. I. Du Pont De Nemours And Company | Acontecimiento de soja DP-305423-1 y composiciones y métodos para su identificación y/o detección |
| 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 |
| ES2432406T3 (es) | 2007-04-05 | 2013-12-03 | Bayer Cropscience Nv | Plantas de algodón resistentes a los insectos y métodos para identificación de las mismas |
| CL2008001592A1 (es) | 2007-05-30 | 2009-03-06 | Syngenta Participations Ag | Celula vegetal que comprende una construccion de acido nucleico que contine una secuencia nucleotidica que codifica un citocromo p450, y metodo para conferir resistencia a un herbicida en la planta basado en la transformacion de la construccion descrita anteriormente. |
| BRPI0813814B1 (pt) | 2007-06-11 | 2018-10-23 | Bayer Bioscience Nv | Método e kit para a identificação de um evento elite em amostras biológicas, par de iniciadores, sonda específica, métodos para a confirmação de pureza de semente, triagem de sementes quanto à presença do evento elite, determinação do estado de zigosidade de uma planta, material de planta ou semente compreendendo o evento elite e detecçãodo evento elite e produção da semente ou planta de algodão |
| BRPI0813044B1 (pt) | 2007-07-31 | 2017-03-21 | Bayer Cropscience Sa | "composto, composição fungicida e método para o controle do fungo fitopatogênico de culturas" |
| WO2009064652A1 (en) | 2007-11-15 | 2009-05-22 | Monsanto Technology Llc | Soybean plant and seed corresponding to transgenic event mon87701 and methods for detection thereof |
| EP2220239B1 (en) | 2007-11-28 | 2015-05-20 | Bayer CropScience NV | 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 |
| CN102119216B (zh) | 2008-02-14 | 2015-05-20 | 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 |
| CN101939437A (zh) | 2008-02-15 | 2011-01-05 | 孟山都技术公司 | 对应于转基因事件mon87769的大豆植物和种子及其检测方法 |
| CN102586236B (zh) | 2008-02-29 | 2014-10-15 | 孟山都技术公司 | 玉米植物事件mon87460以及用于其检测的组合物和方法 |
| CN101998993A (zh) | 2008-04-14 | 2011-03-30 | 拜耳生物科学股份有限公司 | 新的突变羟基苯基丙酮酸双加氧酶,dna序列和耐受hppd抑制剂除草剂的植物分离 |
| US20110152316A1 (en) | 2008-05-22 | 2011-06-23 | Austin Chih-Yu Chen | 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 |
| PL3156488T3 (pl) | 2008-07-17 | 2020-03-31 | BASF Agricultural Solutions Seed US LLC | Roślina Brassica zawierająca zmutowany allel INDEHISCENT |
| US20110268865A1 (en) | 2008-08-01 | 2011-11-03 | Bayer Bio Science N.V. | Method for increasing photosynthetic carbon fixation in rice |
| US9078406B2 (en) | 2008-08-29 | 2015-07-14 | Monsanto Technology Llc | Soybean plant and seed corresponding to transgenic event MON87754 and methods for detection thereof |
| JP5767585B2 (ja) | 2008-09-29 | 2015-08-19 | モンサント テクノロジー エルエルシー | 大豆遺伝子組換え事象mon87705およびその検出方法 |
| ES2635188T3 (es) | 2008-12-16 | 2017-10-02 | Syngenta Participations Ag | Evento de maíz 5307 |
| EA201100945A1 (ru) | 2008-12-19 | 2012-01-30 | Зингента Партисипейшнс Аг | Трансгенный вариант сахарной свеклы gm rz13 |
| CA2748973A1 (en) | 2009-01-07 | 2010-07-15 | Basf Agrochemical Products B.V. | Soybean event 127 and methods related thereto |
| MY176497A (en) | 2009-03-30 | 2020-08-12 | Monsanto Technology Llc | Transgenic rice event 17314 and methods of use thereof |
| US8618359B2 (en) | 2009-03-30 | 2013-12-31 | Monsanto Technology Llc | Rice transgenic event 17053 and methods of use thereof |
| WO2010121818A1 (en) | 2009-04-22 | 2010-10-28 | Bayer Bioscience N.V. | Production of multi-antennary n-glycan structures in plants |
| WO2010145846A1 (en) | 2009-06-15 | 2010-12-23 | Bayer Bioscience N.V. | Nicotiana benthamiana plants deficient in xylosyltransferase activity |
| IN2012DN00427A (enExample) | 2009-07-01 | 2015-05-15 | Bayer Bioscience Nv | |
| UA105046C2 (uk) | 2009-07-02 | 2014-04-10 | Атенікс Корп. | Пестицидний ген axmi-205 та його використання для захисту рослин від комах-шкідників |
| AU2010278843B2 (en) | 2009-07-31 | 2016-05-19 | BASF Agricultural Solutions Seed US LLC | Axmi-192 family of pesticidal genes and methods for their use |
| IN2012DN02294A (enExample) | 2009-08-19 | 2015-08-21 | Dow Agrosciences Llc | |
| EP2478000B1 (en) | 2009-09-17 | 2018-04-11 | Monsanto Technology LLC | Soybean transgenic event mon 87708 and methods of use thereof |
| CN102712911B (zh) | 2009-11-20 | 2016-01-13 | 拜尔作物科学公司 | 包含突变fad3等位基因的芸苔属植物 |
| PT2503873T (pt) | 2009-11-23 | 2017-05-18 | Bayer Cropscience Nv | Plantas de soja tolerantes a herbicida e métodos para identificar as mesmas |
| RU2623176C2 (ru) | 2009-11-23 | 2017-06-22 | Монсанто Текнолоджи Ллс | Трансгенное событие mon 87427 маиса и относительная шкала развития |
| CN104928256A (zh) | 2009-11-24 | 2015-09-23 | 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 |
| WO2011075595A1 (en) | 2009-12-17 | 2011-06-23 | Pioneer Hi-Bred International, Inc. | Maize event dp-043a47-3 and methods for detection thereof |
| US20110154525A1 (en) | 2009-12-17 | 2011-06-23 | Pioneer Hi-Bred International, Inc. | Maize event DP-040416-8 and methods for 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 |
| WO2011084621A1 (en) | 2009-12-17 | 2011-07-14 | Pioneer Hi-Bred International, Inc. | Maize event dp-004114-3 and methods for detection thereof |
| AU2010335573A1 (en) | 2009-12-22 | 2012-06-21 | Bayer Cropscience Nv | Herbicide tolerant plants |
| UY33143A (es) | 2009-12-23 | 2011-07-29 | Bayer Cropscience Ag | Plantas tolerantes a herbicidas inhibidores de las hppd |
| AU2010334808B2 (en) | 2009-12-23 | 2015-07-09 | Bayer Intellectual Property Gmbh | Plants tolerant to HPPD inhibitor herbicides |
| AR079972A1 (es) | 2009-12-23 | 2012-03-07 | Bayer Cropscience Ag | Plantas tolerantes a herbicidas inhibidores de las hppd |
| CA2785211C (en) | 2009-12-23 | 2018-12-11 | Bayer Intellectual Property Gmbh | Plants tolerant to hppd inhibitor herbicides |
| AR080353A1 (es) | 2009-12-23 | 2012-04-04 | Bayer Cropscience Ag | Plantas tolerantes a herbicidas inhibidores de las hppd |
| CN102770544B (zh) | 2010-01-25 | 2015-04-15 | 拜尔作物科学公司 | 制备包含几丁质的植物细胞壁的方法 |
| CA2788238C (en) | 2010-02-04 | 2019-09-03 | Fritz Kreuzaler | A method for increasing photosynthetic carbon fixation using glycolate dehydrogenase multi-subunit fusion protein |
| EP2937419B1 (en) | 2010-02-18 | 2017-08-16 | Athenix Corp. | Axmi221z, axmi222z, axmi223z, axmi224z, and axmi225z delta-endotoxin genes and methods for their use |
| EP2536266A2 (en) | 2010-02-18 | 2012-12-26 | Athenix Corp. | Axmi218, axmi219, axmi220, axmi226, axmi227, axmi228, axmi229, axmi230, and axmi231 delta-endotoxin genes and methods for their use |
| MX2012014066A (es) | 2010-06-04 | 2013-01-24 | Monsanto Technology Llc | Evento de brassica transgenica mon 88302 y metodos para su uso. |
| US8785728B2 (en) | 2010-09-08 | 2014-07-22 | Dow Agrosciences, Llc. | AAD-12 event 1606 and related transgenic soybean lines |
| MX346994B (es) | 2010-10-12 | 2017-04-06 | Monsanto Technology Llc | Planta y semilla de soja correspondiente al evento transgénico mon87712 y métodos para su detección. |
| 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 |
| CA2818918A1 (en) | 2010-11-24 | 2012-05-31 | Pioneer Hi-Bred International, Inc. | Brassica gat event dp-061061-7 and compositions and methods for the identification and/or 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 |
| BR112013015745B1 (pt) | 2010-12-03 | 2021-01-19 | Ms Technologies, Llc | polinucleotídeos referente ao evento de tolerância a herbicida 8291.45.36.2, cassete de expressão, sonda, bem como processos para identificação do evento, determinação da zigosidade, produção de uma planta de soja transgênica e produção de uma proteína em uma célula de planta |
| JP6111200B2 (ja) | 2010-12-03 | 2017-04-05 | ダウ アグロサイエンシィズ エルエルシー | 除草剤耐性イベント8264.44.06.1のスタック、関連するトランスジェニックダイズ系統、およびその検出 |
| 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 |
| BR112013034048B1 (pt) | 2010-12-28 | 2020-11-17 | Toyota Jidosha Kabushiki Kaisha | dna regulador da expressão gênica operacionalmente ligado a uma sequência heteróloga de interesse, e vetor recombinante |
| AU2013333847B2 (en) | 2012-10-19 | 2017-04-20 | Bayer Cropscience Ag | Method for treating plants against fungi resistant to fungicides using carboxamide or thiocarboxamide derivatives |
| AU2013333845B2 (en) | 2012-10-19 | 2017-06-08 | Bayer Cropscience Ag | Method of plant growth promotion using carboxamide derivatives |
| MX381528B (es) | 2012-10-19 | 2025-03-12 | Bayer Cropscience Ag | Método para mejorar la tolerancia al estrés abiótico en plantas usando derivados de carboxamida o tiocarboxamida. |
| UA114528C2 (uk) | 2012-10-19 | 2017-06-26 | Байєр Кропсайнс Аг | Комбінації активних сполук, що містять карбоксамідні похідні та засіб біологічної боротьби |
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-
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- 2017-08-08 AU AU2017213448A patent/AU2017213448B2/en active Active
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010092119A1 (en) * | 2009-02-11 | 2010-08-19 | Basf Se | Dimethomorph as safener for pesticides with phytotoxic effects |
| EP2251331A1 (en) * | 2009-05-15 | 2010-11-17 | Bayer CropScience AG | Fungicide pyrazole carboxamides derivatives |
| WO2010130767A2 (en) * | 2009-05-15 | 2010-11-18 | Bayer Cropscience Ag | Fungicide pyrazole carboxamides derivatives |
| WO2011107443A1 (en) * | 2010-03-02 | 2011-09-09 | Bayer Cropscience Ag | Use of propineb for physiological curative treatment under zinc deficiency |
| WO2012143127A1 (en) * | 2011-04-22 | 2012-10-26 | Bayer Cropsciences Ag | Active compound combinations comprising a (thio)carboxamide derivative and a fungicidal compound |
| WO2012143125A1 (en) * | 2011-04-22 | 2012-10-26 | Bayer Cropscience Ag | Active compound combinations comprising a (thio)carboxamide derivative and an insecticidal or acaricidal or nematicidal active compound |
Non-Patent Citations (1)
| Title |
|---|
| FRANZ J. SCHWINN: "Ergosterol Biosynthesis Inhibitors. An Overview of Their History and Contribution to Medicine and Agriculture", PESTICIDE SCIENCE., ELSEVIER APPLIED SCIENCE PUBLISHER. BARKING., GB, vol. 15, no. 1, 1 February 1984 (1984-02-01), GB, pages 40 - 47, XP002720031, ISSN: 0031-613X, DOI: 10.1002/ps.2780150107 * |
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| AU2017213448A1 (en) | 2017-08-24 |
| AU2013333916A1 (en) | 2015-06-04 |
| JP2015536313A (ja) | 2015-12-21 |
| US20150245610A1 (en) | 2015-09-03 |
| CA2888600A1 (en) | 2014-04-24 |
| CA2888600C (en) | 2021-08-10 |
| EP2908639A1 (en) | 2015-08-26 |
| WO2014060502A1 (en) | 2014-04-24 |
| AR093069A1 (es) | 2015-05-13 |
| US9801374B2 (en) | 2017-10-31 |
| UA114822C2 (uk) | 2017-08-10 |
| EA201590771A1 (ru) | 2015-08-31 |
| AU2017213448B2 (en) | 2018-10-04 |
| JP6153619B2 (ja) | 2017-06-28 |
| AU2013333916B2 (en) | 2017-05-25 |
| CN105357968A (zh) | 2016-02-24 |
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