UA72746C2 - Herbicidal combination and a weed control method - Google Patents
Herbicidal combination and a weed control method Download PDFInfo
- Publication number
- UA72746C2 UA72746C2 UA2001042577A UA2001042577A UA72746C2 UA 72746 C2 UA72746 C2 UA 72746C2 UA 2001042577 A UA2001042577 A UA 2001042577A UA 2001042577 A UA2001042577 A UA 2001042577A UA 72746 C2 UA72746 C2 UA 72746C2
- Authority
- UA
- Ukraine
- Prior art keywords
- carbon atoms
- group
- methyl
- substituted
- alkyl
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title abstract description 36
- 241000196324 Embryophyta Species 0.000 title description 116
- 238000000034 method Methods 0.000 title description 19
- 150000001875 compounds Chemical class 0.000 abstract description 103
- -1 phenoxy methyl group Chemical group 0.000 abstract description 81
- 239000013543 active substance Substances 0.000 abstract description 74
- 239000004009 herbicide Substances 0.000 abstract description 52
- 239000002689 soil Substances 0.000 abstract description 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 19
- 230000002195 synergetic effect Effects 0.000 abstract description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract description 9
- QQOWHRYOXYEMTL-UHFFFAOYSA-N triazin-4-amine Chemical compound N=C1C=CN=NN1 QQOWHRYOXYEMTL-UHFFFAOYSA-N 0.000 abstract description 8
- 239000003666 Amidosulfuron Substances 0.000 abstract description 4
- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 abstract description 4
- CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052801 chlorine Inorganic materials 0.000 abstract description 3
- 229910052731 fluorine Inorganic materials 0.000 abstract description 3
- 125000001153 fluoro group Chemical group F* 0.000 abstract description 3
- BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 abstract description 3
- BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 abstract description 3
- 150000003254 radicals Chemical class 0.000 abstract description 2
- PQKBPHSEKWERTG-UHFFFAOYSA-N Fenoxaprop ethyl Chemical group C1=CC(OC(C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 PQKBPHSEKWERTG-UHFFFAOYSA-N 0.000 abstract 1
- 125000004244 benzofuran-2-yl group Chemical group [H]C1=C(*)OC2=C([H])C([H])=C([H])C([H])=C12 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 description 212
- 125000000217 alkyl group Chemical group 0.000 description 70
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 56
- 239000001257 hydrogen Substances 0.000 description 46
- 229910052739 hydrogen Inorganic materials 0.000 description 46
- 229910052736 halogen Inorganic materials 0.000 description 44
- 150000002367 halogens Chemical class 0.000 description 43
- 150000003839 salts Chemical class 0.000 description 43
- 239000003814 drug Substances 0.000 description 41
- 229940079593 drug Drugs 0.000 description 41
- 239000000203 mixture Substances 0.000 description 39
- 125000005842 heteroatom Chemical group 0.000 description 37
- 229910052757 nitrogen Inorganic materials 0.000 description 37
- 125000000753 cycloalkyl group Chemical group 0.000 description 36
- 229910052760 oxygen Inorganic materials 0.000 description 36
- 239000001301 oxygen Substances 0.000 description 36
- 150000002148 esters Chemical class 0.000 description 35
- 125000000623 heterocyclic group Chemical group 0.000 description 34
- 229910052717 sulfur Inorganic materials 0.000 description 33
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 32
- 230000000694 effects Effects 0.000 description 32
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 30
- 239000011593 sulfur Substances 0.000 description 30
- 150000002431 hydrogen Chemical class 0.000 description 28
- 125000003545 alkoxy group Chemical group 0.000 description 24
- 229910052799 carbon Inorganic materials 0.000 description 22
- 238000011156 evaluation Methods 0.000 description 21
- 238000012360 testing method Methods 0.000 description 20
- 230000006378 damage Effects 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 17
- 125000004429 atom Chemical group 0.000 description 17
- 241000209094 Oryza Species 0.000 description 15
- 241000209140 Triticum Species 0.000 description 15
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- 239000002253 acid Substances 0.000 description 15
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- 235000007164 Oryza sativa Nutrition 0.000 description 14
- 235000009566 rice Nutrition 0.000 description 14
- 125000006413 ring segment Chemical group 0.000 description 14
- 125000003282 alkyl amino group Chemical group 0.000 description 13
- 125000004414 alkyl thio group Chemical group 0.000 description 13
- 125000000304 alkynyl group Chemical group 0.000 description 13
- 239000008187 granular material Substances 0.000 description 13
- 125000001188 haloalkyl group Chemical group 0.000 description 13
- 239000000126 substance Substances 0.000 description 13
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- 235000002017 Zea mays subsp mays Nutrition 0.000 description 12
- 125000003342 alkenyl group Chemical group 0.000 description 12
- 125000004093 cyano group Chemical group *C#N 0.000 description 12
- 125000004494 ethyl ester group Chemical group 0.000 description 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 12
- 125000003118 aryl group Chemical group 0.000 description 11
- 241000209504 Poaceae Species 0.000 description 10
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 10
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 10
- ICJSJAJWTWPSBD-UHFFFAOYSA-N cloquintocet Chemical compound C1=CN=C2C(OCC(=O)O)=CC=C(Cl)C2=C1 ICJSJAJWTWPSBD-UHFFFAOYSA-N 0.000 description 10
- 125000004122 cyclic group Chemical group 0.000 description 10
- 125000005844 heterocyclyloxy group Chemical group 0.000 description 10
- 239000005711 Benzoic acid Substances 0.000 description 9
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 9
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- 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 description 9
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- 239000004215 Carbon black (E152) Substances 0.000 description 8
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 8
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 8
- 239000011575 calcium Substances 0.000 description 8
- 235000005822 corn Nutrition 0.000 description 8
- 150000002430 hydrocarbons Chemical group 0.000 description 8
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 8
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- 238000012545 processing Methods 0.000 description 8
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- 240000005979 Hordeum vulgare Species 0.000 description 7
- 235000007340 Hordeum vulgare Nutrition 0.000 description 7
- 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 7
- 239000000839 emulsion Substances 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 125000005843 halogen group Chemical group 0.000 description 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- 229910052708 sodium Inorganic materials 0.000 description 7
- 159000000000 sodium salts Chemical class 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 125000001424 substituent group Chemical group 0.000 description 7
- 230000000007 visual effect Effects 0.000 description 7
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 6
- 125000002252 acyl group Chemical group 0.000 description 6
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 6
- 150000001721 carbon Chemical group 0.000 description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 6
- 125000004663 dialkyl amino group Chemical group 0.000 description 6
- 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 5
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- 125000002015 acyclic group Chemical group 0.000 description 4
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- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 description 1
- ABOOPXYCKNFDNJ-SNVBAGLBSA-N quizalofop-P Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-SNVBAGLBSA-N 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000005017 substituted alkenyl group Chemical group 0.000 description 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 description 1
- 125000000565 sulfonamide group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
- 125000005329 tetralinyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- UXHMGTYELGTNSJ-UHFFFAOYSA-N triazole-1-carboxamide Chemical compound NC(=O)N1C=CN=N1 UXHMGTYELGTNSJ-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
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000008096 xylene Substances 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/06—Nitrogen directly attached to an aromatic 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)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19842894A DE19842894A1 (de) | 1998-09-18 | 1998-09-18 | Synergistische Wirkstoffkombinationen zur Bekämpfung von Schadpflanzen in Nutzpflanzenkulturen |
| PCT/EP1999/006937 WO2000016627A1 (de) | 1998-09-18 | 1999-09-20 | Synergistische wirkstoffkombinationen zur bekämpfung von schadpflanzen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA72746C2 true UA72746C2 (en) | 2005-04-15 |
Family
ID=7881466
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2001042577A UA72746C2 (en) | 1998-09-18 | 1999-09-20 | Herbicidal combination and a weed control method |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US20040171489A1 (ru) |
| EP (1) | EP1113720B1 (ru) |
| JP (1) | JP4733269B2 (ru) |
| KR (1) | KR100676018B1 (ru) |
| CN (1) | CN1243477C (ru) |
| AT (1) | ATE315336T1 (ru) |
| AU (1) | AU772607B2 (ru) |
| BG (1) | BG65251B1 (ru) |
| BR (2) | BRPI9914496B1 (ru) |
| CA (1) | CA2344394A1 (ru) |
| CZ (1) | CZ303507B6 (ru) |
| DE (2) | DE19842894A1 (ru) |
| ES (1) | ES2257099T3 (ru) |
| HR (1) | HRP20010193B1 (ru) |
| HU (1) | HU229822B1 (ru) |
| ID (1) | ID29884A (ru) |
| IL (2) | IL142032A0 (ru) |
| NZ (1) | NZ510192A (ru) |
| PL (1) | PL200240B1 (ru) |
| PT (1) | PT1113720E (ru) |
| RU (1) | RU2261598C9 (ru) |
| SK (1) | SK287091B6 (ru) |
| TR (1) | TR200100781T2 (ru) |
| UA (1) | UA72746C2 (ru) |
| WO (1) | WO2000016627A1 (ru) |
| ZA (1) | ZA200102106B (ru) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19960684A1 (de) * | 1999-12-15 | 2001-06-21 | Aventis Cropscience Gmbh | Kombinationen von herbiziden Alkylazinen und Safenern |
| GB0022932D0 (en) | 2000-09-18 | 2000-11-01 | Aventis Cropscience Sa | New herbicidal composition |
| GB0022835D0 (en) | 2000-09-18 | 2000-11-01 | Aventis Cropscience Sa | New herbicidal composition |
| GB0022833D0 (en) | 2000-09-18 | 2000-11-01 | Aventis Cropscience Sa | New herbicidal composition |
| DE10117505A1 (de) * | 2001-04-07 | 2002-10-10 | Bayer Cropscience Gmbh | Synergistische Wirkstoffkombinationen zur Bekämpfung von Schadpflanzen |
| DE10209430A1 (de) | 2002-03-05 | 2003-09-18 | Bayer Cropscience Gmbh | Herbizid-Kombination mit acylierten Aminophenylsulfonylharnstoffen |
| DE10209468A1 (de) * | 2002-03-05 | 2003-09-18 | Bayer Cropscience Gmbh | Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen |
| DE102004034571A1 (de) | 2004-07-17 | 2006-02-23 | Bayer Cropscience Gmbh | Herbizide Mittel |
| EP1790227A1 (de) | 2005-11-25 | 2007-05-30 | Bayer CropScience AG | Wässrige Suspensionskonzentrate aus 2,4-Diamino-s-triazinherbiziden |
| RU2308833C2 (ru) * | 2005-12-19 | 2007-10-27 | Государственное научное учреждение Нижне-Волжский научно-исследовательский институт сельского хозяйства РАСХН (ГНУ НВ НИИСХ) | Средство, способ его получения и способ борьбы с трудноискоренимым карантинным сорняком горчаком ползучим с использованием средства |
| EP1854355A1 (de) * | 2006-03-15 | 2007-11-14 | Bayer CropScience AG | Wässrige Suspensionskonzentrate |
| EP1958509A1 (de) * | 2007-02-19 | 2008-08-20 | Bayer CropScience AG | Herbizid-Kombination |
| US20090215625A1 (en) * | 2008-01-07 | 2009-08-27 | Auburn University | Combinations of Herbicides and Safeners |
| CA2714560A1 (en) * | 2008-02-12 | 2009-08-20 | Arysta Lifescience North America, Llc | Method of controlling unwanted vegetation |
| EP2092825A1 (de) * | 2008-02-21 | 2009-08-26 | Bayer CropScience Aktiengesellschaft | Herbizid-Kombinationen enthaltend ein Herbizid der Klasse der Diamino-s-triazine |
| PT2555615E (pt) * | 2010-02-19 | 2014-05-29 | Dow Agrosciences Llc | Composição herbicida/fungicida sinérgica contendo ácido 4-amino-3-cloro-6-(4-cloro-2-fluoro-3-metoxifenil)- -piridina-2-carboxílico e um fungicida |
| KR20130091729A (ko) | 2010-07-20 | 2013-08-19 | 베스타론 코포레이션 | 살충제 트라이아진 및 피리미딘 |
| CN101926349A (zh) * | 2010-09-13 | 2010-12-29 | 尹小根 | 一组含有酰嘧磺隆与莠去津的除草组合物 |
| US8916183B2 (en) * | 2012-02-02 | 2014-12-23 | Dow Agrosciences, Llc. | Pesticidal compositions and processes related thereto |
| US8916499B2 (en) * | 2012-07-24 | 2014-12-23 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and a protoporphyrinogen oxidase inhibitor |
| CN102986706B (zh) * | 2012-12-20 | 2014-02-26 | 联保作物科技有限公司 | 一种水稻田除草组合物 |
| CA2941360A1 (en) * | 2014-04-23 | 2015-10-29 | Basf Se | Herbicidal combination comprising azines |
| JP2018514536A (ja) | 2015-04-27 | 2018-06-07 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | グルホシネートおよびインダジフラムを含む除草剤組み合わせ |
| US10912301B2 (en) | 2015-05-11 | 2021-02-09 | Basf Se | Herbicide combinations comprising L-glufosinate and indaziflam |
| CA3130265A1 (en) | 2019-02-19 | 2020-08-27 | Gowan Company, L.L.C. | Stable liquid compositions and methods of using the same |
| JP7620649B2 (ja) | 2020-06-10 | 2025-01-23 | アリゴス セラピューティクス インコーポレイテッド | コロナウイルス、ピコルナウイルス及びノロウイルス感染を治療するための抗ウイルス化合物 |
| CA3224494A1 (en) | 2021-07-09 | 2023-01-12 | Koen Vandyck | Anti-viral compounds |
| US12065428B2 (en) | 2021-09-17 | 2024-08-20 | Aligos Therapeutics, Inc. | Anti-viral compounds |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0477403A (ja) * | 1990-07-20 | 1992-03-11 | Idemitsu Kosan Co Ltd | 除草剤組成物 |
| JPH0489409A (ja) * | 1990-08-01 | 1992-03-23 | Idemitsu Kosan Co Ltd | 除草剤組成物 |
| JPH0495003A (ja) * | 1990-08-13 | 1992-03-27 | Idemitsu Kosan Co Ltd | 除草剤組成物 |
| JPH0495004A (ja) * | 1990-08-13 | 1992-03-27 | Idemitsu Kosan Co Ltd | 除草剤組成物 |
| JP2908853B2 (ja) * | 1990-08-15 | 1999-06-21 | 出光興産株式会社 | 除草剤組成物 |
| EP0557308B2 (de) * | 1990-11-13 | 2001-03-28 | Aventis CropScience GmbH | Synergistische herbizide mittel |
| DE4223465A1 (de) * | 1992-07-16 | 1994-01-20 | Bayer Ag | Herbizide Mittel auf Basis von Heteroaryloxyacetamiden |
| JPH07267805A (ja) * | 1994-03-28 | 1995-10-17 | Idemitsu Kosan Co Ltd | 芝生用除草剤組成物 |
| JPH07267804A (ja) * | 1994-03-28 | 1995-10-17 | Idemitsu Kosan Co Ltd | 除草剤組成物 |
| JPH08198712A (ja) * | 1995-01-26 | 1996-08-06 | Idemitsu Kosan Co Ltd | 除草剤組成物 |
| DE19531084A1 (de) * | 1995-08-24 | 1997-02-27 | Hoechst Schering Agrevo Gmbh | 2,4-Diamino-1,3,5-triazine, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| DE19607450A1 (de) * | 1996-02-28 | 1997-09-04 | Hoechst Schering Agrevo Gmbh | 2-Amino-4-bicycloamino-1,3,5-triazine, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| WO1997035481A1 (en) * | 1996-03-22 | 1997-10-02 | Idemitsu Kosan Co., Ltd. | Herbicidal composition |
| DE19641693A1 (de) * | 1996-10-10 | 1998-04-16 | Bayer Ag | Substituierte 2-Amino-4-alkylamino-1,3,5-triazine |
| DE19641691A1 (de) * | 1996-10-10 | 1998-04-16 | Bayer Ag | Substituierte 2-Amino-4-alkylamino-1,3,5-triazine |
| DE19641694A1 (de) * | 1996-10-10 | 1998-04-16 | Bayer Ag | Substituierte 2,4-Diamino-1,3,5-triazine |
| DE19641692A1 (de) * | 1996-10-10 | 1998-04-23 | Bayer Ag | Substituierte 2,4-Diamino-1,3,5-triazine |
| DE19704922A1 (de) * | 1997-02-10 | 1998-08-13 | Hoechst Schering Agrevo Gmbh | 2,4-Diamino-1,3,5-triazine, ihre Herstellung und Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| DE19711825A1 (de) * | 1997-03-21 | 1998-09-24 | Bayer Ag | Substituierte 2,4-Diamino-1,3,5-triazine |
| DE19744232A1 (de) * | 1997-10-07 | 1999-04-08 | Bayer Ag | Substituierte 2,4-Diamino-1,3,5-triazine |
| DE19744711A1 (de) * | 1997-10-10 | 1999-04-15 | Bayer Ag | Substituierte 2,4-Diamino-1,3,5-triazine |
| DE19802236A1 (de) * | 1998-01-22 | 1999-07-29 | Bayer Ag | Substituierte Aminoalkylidenaminotriazine |
| HUP0102663A3 (en) * | 1998-06-16 | 2002-03-28 | Aventis Cropscience Gmbh | Herbicidal 2,4-diamino-1,3,5-triazines, intermediates, preparation and use thereof |
| DE19828519A1 (de) * | 1998-06-26 | 1999-12-30 | Hoechst Schering Agrevo Gmbh | Substituierte 2,4-Diamino-1,3,5-triazine, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
-
1998
- 1998-09-18 DE DE19842894A patent/DE19842894A1/de not_active Withdrawn
-
1999
- 1999-09-20 SK SK377-2001A patent/SK287091B6/sk not_active IP Right Cessation
- 1999-09-20 BR BRPI9914496A patent/BRPI9914496B1/pt active IP Right Grant
- 1999-09-20 NZ NZ510192A patent/NZ510192A/en not_active IP Right Cessation
- 1999-09-20 DE DE59913050T patent/DE59913050D1/de not_active Expired - Lifetime
- 1999-09-20 AT AT99969311T patent/ATE315336T1/de not_active IP Right Cessation
- 1999-09-20 CA CA002344394A patent/CA2344394A1/en not_active Abandoned
- 1999-09-20 JP JP2000573598A patent/JP4733269B2/ja not_active Expired - Lifetime
- 1999-09-20 UA UA2001042577A patent/UA72746C2/uk unknown
- 1999-09-20 HR HR20010193A patent/HRP20010193B1/xx not_active IP Right Cessation
- 1999-09-20 ES ES99969311T patent/ES2257099T3/es not_active Expired - Lifetime
- 1999-09-20 AU AU59796/99A patent/AU772607B2/en not_active Expired
- 1999-09-20 EP EP99969311A patent/EP1113720B1/de not_active Expired - Lifetime
- 1999-09-20 HU HU0104269A patent/HU229822B1/hu unknown
- 1999-09-20 PT PT99969311T patent/PT1113720E/pt unknown
- 1999-09-20 PL PL346878A patent/PL200240B1/pl unknown
- 1999-09-20 KR KR1020017003489A patent/KR100676018B1/ko not_active Expired - Lifetime
- 1999-09-20 ID IDW20010614A patent/ID29884A/id unknown
- 1999-09-20 CZ CZ20010986A patent/CZ303507B6/cs not_active IP Right Cessation
- 1999-09-20 WO PCT/EP1999/006937 patent/WO2000016627A1/de not_active Ceased
- 1999-09-20 IL IL14203299A patent/IL142032A0/xx active IP Right Grant
- 1999-09-20 RU RU2001107142/04A patent/RU2261598C9/ru active
- 1999-09-20 TR TR2001/00781T patent/TR200100781T2/xx unknown
- 1999-09-20 CN CNB99811054XA patent/CN1243477C/zh not_active Expired - Lifetime
- 1999-09-20 BR BRPI9917835-4A patent/BR9917835B1/pt active IP Right Grant
-
2001
- 2001-03-09 BG BG105324A patent/BG65251B1/bg unknown
- 2001-03-14 ZA ZA200102106A patent/ZA200102106B/en unknown
- 2001-03-15 IL IL142032A patent/IL142032A/en not_active IP Right Cessation
-
2003
- 2003-12-12 US US10/734,792 patent/US20040171489A1/en not_active Abandoned
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