ES2329592T3 - Combinacion de herbicidas y antidotos. - Google Patents
Combinacion de herbicidas y antidotos. Download PDFInfo
- Publication number
- ES2329592T3 ES2329592T3 ES05716020T ES05716020T ES2329592T3 ES 2329592 T3 ES2329592 T3 ES 2329592T3 ES 05716020 T ES05716020 T ES 05716020T ES 05716020 T ES05716020 T ES 05716020T ES 2329592 T3 ES2329592 T3 ES 2329592T3
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- case
- halogen
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- alkyl
- Prior art date
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- 239000004009 herbicide Substances 0.000 title claims abstract description 71
- 239000000729 antidote Substances 0.000 title claims abstract description 61
- 229940075522 antidotes Drugs 0.000 title claims abstract description 56
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 43
- 150000002367 halogens Chemical class 0.000 claims abstract description 43
- 239000001257 hydrogen Substances 0.000 claims abstract description 41
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 41
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 39
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 37
- 150000001875 compounds Chemical class 0.000 claims abstract description 30
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 25
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract description 19
- 125000003282 alkyl amino group Chemical group 0.000 claims abstract description 18
- 150000003839 salts Chemical class 0.000 claims abstract description 17
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 15
- 125000000304 alkynyl group Chemical group 0.000 claims abstract description 13
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 13
- YNQSILKYZQZHFJ-UHFFFAOYSA-N R-29148 Chemical compound CC1CN(C(=O)C(Cl)Cl)C(C)(C)O1 YNQSILKYZQZHFJ-UHFFFAOYSA-N 0.000 claims abstract description 12
- 125000003118 aryl group Chemical group 0.000 claims abstract description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 11
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 10
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims abstract description 10
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims abstract description 10
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 10
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 claims abstract description 9
- YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 claims abstract description 9
- MKQSWTQPLLCSOB-UHFFFAOYSA-N benzyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound N1=C(Cl)SC(C(=O)OCC=2C=CC=CC=2)=C1C(F)(F)F MKQSWTQPLLCSOB-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000004663 dialkyl amino group Chemical group 0.000 claims abstract description 9
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims abstract description 8
- RFMQOHXWHFHOJF-UHFFFAOYSA-N cyano thiocyanate Chemical compound N#CSC#N RFMQOHXWHFHOJF-UHFFFAOYSA-N 0.000 claims abstract description 8
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 claims abstract description 8
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 8
- COYBRKAVBMYYSF-UHFFFAOYSA-N heptan-2-yl [(5-chloroquinolin-8-yl)oxy]acetate Chemical group C1=CN=C2C(OCC(=O)OC(C)CCCCC)=CC=C(Cl)C2=C1 COYBRKAVBMYYSF-UHFFFAOYSA-N 0.000 claims abstract description 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 7
- DOFZAZXDOSGAJZ-UHFFFAOYSA-N disulfoton Chemical compound CCOP(=S)(OCC)SCCSCC DOFZAZXDOSGAJZ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 4
- JCHMGYRXQDASJE-UHFFFAOYSA-N metcamifen Chemical compound C1=CC(NC(=O)NC)=CC=C1S(=O)(=O)NC(=O)C1=CC=CC=C1OC JCHMGYRXQDASJE-UHFFFAOYSA-N 0.000 claims abstract description 4
- NYDKNJDNBUFWRJ-UHFFFAOYSA-N n-[4-(dimethylcarbamoylamino)phenyl]sulfonyl-2-methoxybenzamide Chemical compound COC1=CC=CC=C1C(=O)NS(=O)(=O)C1=CC=C(NC(=O)N(C)C)C=C1 NYDKNJDNBUFWRJ-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 3
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims abstract description 3
- OAWUUPVZMNKZRY-UHFFFAOYSA-N cyprosulfamide Chemical compound COC1=CC=CC=C1C(=O)NS(=O)(=O)C1=CC=C(C(=O)NC2CC2)C=C1 OAWUUPVZMNKZRY-UHFFFAOYSA-N 0.000 claims abstract 2
- MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical group C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 claims description 161
- 239000000203 mixture Substances 0.000 claims description 39
- 239000013543 active substance Substances 0.000 claims description 33
- 230000002363 herbicidal effect Effects 0.000 claims description 31
- 238000009472 formulation Methods 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 22
- 239000000126 substance Substances 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 17
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- 125000004429 atom Chemical group 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 6
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- 244000038559 crop plants Species 0.000 claims description 6
- 150000008065 acid anhydrides Chemical class 0.000 claims description 5
- 235000013311 vegetables Nutrition 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 abstract description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 89
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- 150000003254 radicals Chemical class 0.000 description 23
- 150000002431 hydrogen Chemical class 0.000 description 21
- 235000010469 Glycine max Nutrition 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 14
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 13
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- 229910052801 chlorine Inorganic materials 0.000 description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 240000008042 Zea mays Species 0.000 description 9
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 9
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 9
- 235000013339 cereals Nutrition 0.000 description 9
- 235000005822 corn Nutrition 0.000 description 9
- 125000000623 heterocyclic group Chemical group 0.000 description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
- 240000007594 Oryza sativa Species 0.000 description 8
- 235000007164 Oryza sativa Nutrition 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 125000001153 fluoro group Chemical group F* 0.000 description 8
- 125000005842 heteroatom Chemical group 0.000 description 8
- 229910052760 oxygen Inorganic materials 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 235000009566 rice Nutrition 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 125000001309 chloro group Chemical group Cl* 0.000 description 7
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 7
- 229910052717 sulfur Inorganic materials 0.000 description 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 7
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- 235000007319 Avena orientalis Nutrition 0.000 description 6
- 240000002791 Brassica napus Species 0.000 description 6
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 244000062793 Sorghum vulgare Species 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
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- 239000008187 granular material Substances 0.000 description 6
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- 125000006413 ring segment Chemical group 0.000 description 5
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- 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 description 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
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- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 3
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical compound CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 1
- 229960003231 thioacetazone Drugs 0.000 description 1
- 150000003566 thiocarboxylic acids Chemical class 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- 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
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
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)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004015140 | 2004-03-27 | ||
| DE102004015140 | 2004-03-27 | ||
| DE102004031345 | 2004-06-30 | ||
| DE102004031345 | 2004-06-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2329592T3 true ES2329592T3 (es) | 2009-11-27 |
Family
ID=34962868
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES05716020T Expired - Lifetime ES2329592T3 (es) | 2004-03-27 | 2005-03-12 | Combinacion de herbicidas y antidotos. |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7563749B2 (https=) |
| EP (1) | EP1732391B1 (https=) |
| JP (1) | JP2007530473A (https=) |
| KR (1) | KR20060131926A (https=) |
| AR (1) | AR050143A1 (https=) |
| AT (1) | ATE442044T1 (https=) |
| AU (1) | AU2005226870B2 (https=) |
| BR (1) | BRPI0509289A (https=) |
| CA (1) | CA2560908A1 (https=) |
| CR (1) | CR8557A (https=) |
| DE (1) | DE502005008105D1 (https=) |
| EA (1) | EA011892B1 (https=) |
| ES (1) | ES2329592T3 (https=) |
| IL (1) | IL178033A0 (https=) |
| PL (1) | PL1732391T3 (https=) |
| PT (1) | PT1732391E (https=) |
| UA (1) | UA84201C2 (https=) |
| WO (1) | WO2005092103A1 (https=) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EA011812B1 (ru) * | 2004-03-27 | 2009-06-30 | Байер Кропсайенс Аг | Комбинация гербицидов |
| EP1728430A1 (de) * | 2005-06-04 | 2006-12-06 | Bayer CropScience GmbH | Herbizide Mittel |
| 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 |
| BR122017006111B8 (pt) | 2006-10-31 | 2022-12-06 | Du Pont | Métodos para controlar ervas daninhas |
| EP2145537A1 (en) * | 2008-07-09 | 2010-01-20 | Bayer CropScience AG | Plant growth regulator |
| AU2010209649B2 (en) * | 2009-02-02 | 2015-01-22 | Basf Se | Herbicidal compositions comprising naptalam |
| EP2255637A1 (en) * | 2009-05-02 | 2010-12-01 | Bayer CropScience AG | Method for weed control in lawn or turf |
| BR112012029397B1 (pt) * | 2010-05-17 | 2018-08-28 | Nufarm Australia Ltd | processo para a preparação de sais de amina sólidos de herbicidas à base de ácido carboxílico aromático substituído |
| CN103237894A (zh) | 2010-08-13 | 2013-08-07 | 先锋国际良种公司 | 包含具有羟基苯丙酮酸双加氧酶(hppd)活性的序列的组合物和方法 |
| 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 |
| WO2012071040A1 (en) | 2010-11-24 | 2012-05-31 | Pioneer Hi-Bred International, Inc. | Brassica gat event dp-073496-4 and compositions and methods for the identification and/or 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 |
| US9247735B2 (en) * | 2011-01-19 | 2016-02-02 | Rotam Agrochem International Company Limited | Crop plant-compatible herbicidal compositions containing herbicides and safeners |
| CA2848622A1 (en) * | 2011-09-16 | 2013-03-21 | Bayer Intellectual Property Gmbh | Use of 5-phenyl- or 5-benzyl-2-isoxazoline-3-carboxylates for improving plant yield |
| WO2013188291A2 (en) | 2012-06-15 | 2013-12-19 | E. I. Du Pont De Nemours And Company | Methods and compositions involving als variants with native substrate preference |
| CA2894213A1 (en) | 2012-12-21 | 2014-06-26 | Pioneer Hi-Bred International, Inc. | Compositions and methods for auxin-analog conjugation |
| WO2014159306A1 (en) | 2013-03-13 | 2014-10-02 | Pioneer Hi-Bred International, Inc. | Glyphosate application for weed control in brassica |
| BR112015023286A2 (pt) | 2013-03-14 | 2018-03-06 | Arzeda Corp | polipeptídeo recombinante com atividade da dicamba descarboxilase, construto de polinucleotídeo, célula, método de produção de uma célula hospedeira compreendendo um polinucleotídeo heterólogo que codifica um polipeptídeo tendo atividade da dicamba descarboxilase, método para descarboxilar dicamba, um derivado de dicamba ou um metabolito de dicamba, método para a detecção de um polipeptideo e método para a detecção da presença de um polinucleotideo que codifica um polipeptideo tendo atividade da dicamba descarboxilase |
| AU2014236154A1 (en) | 2013-03-14 | 2015-09-17 | Pioneer Hi-Bred International, Inc. | Compositions having dicamba decarboxylase activity and methods of use |
| US10329578B2 (en) | 2013-10-18 | 2019-06-25 | Pioneer Hi-Bred International, Inc. | Glyphosate-N-acetyltransferase (GLYAT) sequences and methods of use |
| WO2018029104A1 (de) | 2016-08-11 | 2018-02-15 | Bayer Cropscience Aktiengesellschaft | Substituierte pyrazolinylderivate, verfahren zu deren herstellung und ihre verwendung als herbizide und/oder pflanzenwachstumsregulatoren |
| GB2555462B (en) * | 2016-10-31 | 2021-07-07 | Rotam Agrochem Int Co Ltd | Herbicidal composition comprising mesotrione |
| WO2025015330A2 (en) * | 2023-07-13 | 2025-01-16 | The Board Of Trustees Of The University Of Arkansas | Enhancing tolerance of rice to bleaching herbicides with a fenclorim seed treatment |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4137070A (en) | 1971-04-16 | 1979-01-30 | Stauffer Chemical Company | Herbicide compositions |
| US4021224A (en) | 1971-12-09 | 1977-05-03 | Stauffer Chemical Company | Herbicide compositions |
| US4021229A (en) | 1972-09-05 | 1977-05-03 | Stauffer Chemical Company | Sulfonamide herbicide antidote compositions and method of use |
| 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. |
| MX159669A (es) | 1983-12-12 | 1989-08-02 | Ciba Geigy Ag | Procedimiento para la preparacion de derivados de acilamida |
| US4601745A (en) | 1983-12-12 | 1986-07-22 | Ciba-Geigy Corporation | Composition for the protection of cultivated plants against the phytotoxic action of herbicides |
| 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 |
| DE3633840A1 (de) | 1986-10-04 | 1988-04-14 | Hoechst Ag | Phenylpyrazolcarbonsaeurederivate, ihre herstellung und verwendung als pflanzenwachstumsregulatoren und safener |
| DE3808896A1 (de) | 1988-03-17 | 1989-09-28 | Hoechst Ag | Pflanzenschuetzende mittel auf basis von pyrazolcarbonsaeurederivaten |
| 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 |
| US5215570A (en) | 1988-10-20 | 1993-06-01 | Ciba-Geigy Corporation | Sulfamoylphenylureas |
| ES2054088T3 (es) | 1988-10-20 | 1994-08-01 | Ciba Geigy Ag | Sulfamoilfenilureas. |
| 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 |
| US5700758A (en) | 1989-11-30 | 1997-12-23 | Hoechst Aktiengesellschaft | Pyrazolines for protecting crop plants against herbicides |
| EP0492367B1 (de) | 1990-12-21 | 2000-09-27 | Aventis CropScience GmbH | Mischungen aus Herbiziden und Antidots |
| 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 |
| TW259690B (https=) | 1992-08-01 | 1995-10-11 | Hoechst Ag | |
| DE4323122A1 (de) * | 1993-07-10 | 1995-01-12 | Hoechst Schering Agrevo Gmbh | Mischungen aus Herbiziden und Antidots |
| 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 |
| DE4336875A1 (de) * | 1993-09-27 | 1995-03-30 | Bayer Ag | N-Azinyl-N'-(het)arylsulfonyl-harnstoffe |
| DE19621522A1 (de) | 1996-05-29 | 1997-12-04 | Hoechst Schering Agrevo Gmbh | Neue N-Acylsulfonamide, neue Mischungen aus Herbiziden und Antidots und deren Verwendung |
| DE19742951A1 (de) | 1997-09-29 | 1999-04-15 | Hoechst Schering Agrevo Gmbh | Acylsulfamoylbenzoesäureamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung |
| AR031027A1 (es) | 2000-10-23 | 2003-09-03 | Syngenta Participations Ag | Composiciones agroquimicas |
| BR0206859A (pt) * | 2001-01-31 | 2004-01-13 | Bayer Cropscience Gmbh | Método para proteger colheitas empregando carboxilatos de isoxazolina |
-
2005
- 2005-03-12 BR BRPI0509289-2A patent/BRPI0509289A/pt not_active IP Right Cessation
- 2005-03-12 UA UAA200611344A patent/UA84201C2/ru unknown
- 2005-03-12 WO PCT/EP2005/002672 patent/WO2005092103A1/de not_active Ceased
- 2005-03-12 EA EA200601704A patent/EA011892B1/ru not_active IP Right Cessation
- 2005-03-12 JP JP2007504300A patent/JP2007530473A/ja active Pending
- 2005-03-12 PT PT05716020T patent/PT1732391E/pt unknown
- 2005-03-12 ES ES05716020T patent/ES2329592T3/es not_active Expired - Lifetime
- 2005-03-12 DE DE502005008105T patent/DE502005008105D1/de not_active Expired - Lifetime
- 2005-03-12 KR KR1020067020021A patent/KR20060131926A/ko not_active Ceased
- 2005-03-12 EP EP05716020A patent/EP1732391B1/de not_active Expired - Lifetime
- 2005-03-12 CA CA002560908A patent/CA2560908A1/en not_active Abandoned
- 2005-03-12 AU AU2005226870A patent/AU2005226870B2/en not_active Ceased
- 2005-03-12 AT AT05716020T patent/ATE442044T1/de active
- 2005-03-12 PL PL05716020T patent/PL1732391T3/pl unknown
- 2005-03-23 AR ARP050101172A patent/AR050143A1/es not_active Application Discontinuation
- 2005-03-25 US US11/090,985 patent/US7563749B2/en not_active Expired - Fee Related
-
2006
- 2006-08-11 CR CR8557A patent/CR8557A/es not_active Application Discontinuation
- 2006-09-12 IL IL178033A patent/IL178033A0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PL1732391T3 (pl) | 2010-02-26 |
| AU2005226870A1 (en) | 2005-10-06 |
| IL178033A0 (en) | 2006-12-31 |
| EP1732391A1 (de) | 2006-12-20 |
| UA84201C2 (en) | 2008-09-25 |
| US7563749B2 (en) | 2009-07-21 |
| CR8557A (es) | 2008-02-28 |
| AU2005226870B2 (en) | 2010-06-10 |
| DE502005008105D1 (de) | 2009-10-22 |
| EA011892B1 (ru) | 2009-06-30 |
| PT1732391E (pt) | 2009-11-18 |
| KR20060131926A (ko) | 2006-12-20 |
| BRPI0509289A (pt) | 2007-09-18 |
| EP1732391B1 (de) | 2009-09-09 |
| EA200601704A1 (ru) | 2007-02-27 |
| US20050233904A1 (en) | 2005-10-20 |
| WO2005092103A1 (de) | 2005-10-06 |
| AR050143A1 (es) | 2006-10-04 |
| CA2560908A1 (en) | 2005-10-06 |
| JP2007530473A (ja) | 2007-11-01 |
| ATE442044T1 (de) | 2009-09-15 |
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