UA72490C2 - Фунгицидная смесь и способ борьбы с фитопатогенными грибами - Google Patents
Фунгицидная смесь и способ борьбы с фитопатогенными грибами Download PDFInfo
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- UA72490C2 UA72490C2 UA2001075221A UA2001075221A UA72490C2 UA 72490 C2 UA72490 C2 UA 72490C2 UA 2001075221 A UA2001075221 A UA 2001075221A UA 2001075221 A UA2001075221 A UA 2001075221A UA 72490 C2 UA72490 C2 UA 72490C2
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- compounds
- compound
- halogen
- fungicidal mixture
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- 239000000203 mixture Substances 0.000 title claims abstract description 47
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 15
- 241000233866 Fungi Species 0.000 title claims description 15
- 230000003032 phytopathogenic effect Effects 0.000 title claims description 14
- 238000000034 method Methods 0.000 title claims description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 58
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 13
- 150000002367 halogens Chemical class 0.000 claims abstract description 13
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 8
- 239000001257 hydrogen Substances 0.000 claims abstract description 8
- 125000003118 aryl group Chemical group 0.000 claims abstract description 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 6
- 150000003839 salts Chemical class 0.000 claims abstract description 6
- 125000004104 aryloxy group Chemical group 0.000 claims abstract description 3
- 150000004657 carbamic acid derivatives Chemical class 0.000 claims abstract 2
- 239000013543 active substance Substances 0.000 claims description 22
- -1 surfaces Substances 0.000 claims description 16
- 239000007787 solid Substances 0.000 claims description 6
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- 239000005778 Fenpropimorph Substances 0.000 claims description 5
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- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 claims description 3
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- 125000001424 substituent group Chemical group 0.000 claims description 3
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- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- 239000007788 liquid Substances 0.000 claims 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
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- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical class N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 235000021015 bananas Nutrition 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical group 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 235000016213 coffee Nutrition 0.000 description 1
- 235000013353 coffee beverage Nutrition 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 description 1
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 description 1
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229940071870 hydroiodic acid Drugs 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 238000001182 laser chemical vapour deposition Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000004672 propanoic acids Chemical class 0.000 description 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000000080 wetting agent 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
- 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
-
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
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)
- Pretreatment Of Seeds And Plants (AREA)
- Quinoline Compounds (AREA)
Abstract
Изобретение касается фунгицидной смеси, содержащей в качестве активных компонентов а) соединение формулы I ,(I) его N-оксид или одну из ее солей, причем заместители имеют такое значение: R1, R2, R3, R4 независимо один от другого означают водород, гидрокси, нитро, галоген, С1-C4алкил, С1-C4галогеналкил, С1-C4алкокси, С1-C4галогеналкокси, С1-C4алкилтио, С1-C4галогеналкилтио; R5, R6, R7 независимо один от другого означают: водород, гидрокси, циано, нитро, галоген, С1-C7алкил, С1-C7галогеналкил, С1-C7алкокси, С1-C7галогеналкокси, С1-C7алкилтио, С1-C7галогеналкилтио, С1-C7гидроксиалкил, С2-С4ацил, арил, арилокси, причем остатки с арилом в свою очередь могут иметь от одной до трех групп, выбранных из группы, куда входят: циано, нитро, галоген, С1-C4алкил, С1-C4галогеналкил, С1-C4алкокси, С1-C4галогеналкокси, С1-C4алкилтио и С1-C4галогеналкилтио, и б) карбаматы формулы II ,(II) где Τ означает СН или Ν, n имеет значение 0, 1 или 2 и R означает галоген, С1-C4алкил или С1-C4галогеналкил, причем остатки R могут быть различными, если n равно 2, в синергетичнo эффективном количестве.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19859250 | 1998-12-22 | ||
| PCT/EP1999/009812 WO2000036921A1 (de) | 1998-12-22 | 1999-12-11 | Fungizide mischung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA72490C2 true UA72490C2 (ru) | 2005-03-15 |
Family
ID=7892105
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2001075221A UA72490C2 (ru) | 1998-12-22 | 1999-11-12 | Фунгицидная смесь и способ борьбы с фитопатогенными грибами |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US6541500B1 (ru) |
| EP (1) | EP1139758B1 (ru) |
| JP (1) | JP4570785B2 (ru) |
| KR (1) | KR100692507B1 (ru) |
| CN (1) | CN1293809C (ru) |
| AR (1) | AR021992A1 (ru) |
| AT (1) | ATE238665T1 (ru) |
| AU (1) | AU769532B2 (ru) |
| BR (1) | BR9916453B1 (ru) |
| CA (1) | CA2355711C (ru) |
| CO (1) | CO5221028A1 (ru) |
| CZ (1) | CZ301438B6 (ru) |
| DE (1) | DE59905365D1 (ru) |
| DK (1) | DK1139758T3 (ru) |
| EA (1) | EA004293B1 (ru) |
| ES (1) | ES2198982T3 (ru) |
| HU (1) | HU229238B1 (ru) |
| IL (2) | IL143448A0 (ru) |
| NZ (1) | NZ512934A (ru) |
| PL (1) | PL198429B1 (ru) |
| PT (1) | PT1139758E (ru) |
| SK (1) | SK284861B6 (ru) |
| TW (1) | TW529909B (ru) |
| UA (1) | UA72490C2 (ru) |
| WO (1) | WO2000036921A1 (ru) |
| ZA (1) | ZA200105979B (ru) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA72490C2 (ru) * | 1998-12-22 | 2005-03-15 | Басф Акцієнгезелльшафт | Фунгицидная смесь и способ борьбы с фитопатогенными грибами |
| DE10144991A1 (de) * | 2001-09-12 | 2003-03-27 | Basf Ag | Fungizide Mischungen |
| NZ586470A (en) * | 2002-03-07 | 2011-11-25 | Basf Se | Fungicidal mixture comprising 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione (prothioconazole) and triticonazole |
| CN100348105C (zh) * | 2003-10-01 | 2007-11-14 | 巴斯福股份公司 | 杀真菌剂混合物 |
| US7338967B2 (en) * | 2004-09-10 | 2008-03-04 | Syngenta Limited | Substituted isoxazoles as fungicides |
| JP2011201857A (ja) * | 2010-03-03 | 2011-10-13 | Sumitomo Chemical Co Ltd | 植物病害防除組成物及び植物病害防除方法 |
| AU2015202125B2 (en) * | 2010-03-03 | 2015-12-03 | Sumitomo Chemical Company, Limited | Plant disease controlling composition and method for controlling plant disease |
| WO2011123943A1 (en) | 2010-04-09 | 2011-10-13 | Mount Sinai Hospital | Methods for treating disorders of the gastrointestinal tract using a glp-1 agonist |
| CN103444743B (zh) * | 2012-06-02 | 2016-12-07 | 陕西韦尔奇作物保护有限公司 | 一种含苯氧喹啉与甲氧基丙烯酸酯类的杀菌组合物 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL89029A (en) * | 1988-01-29 | 1993-01-31 | Lilly Co Eli | Fungicidal quinoline and cinnoline derivatives, compositions containing them, and fungicidal methods of using them |
| ATE172360T1 (de) * | 1994-07-21 | 1998-11-15 | Basf Ag | Verfahren zur bekämpfung von schadpilzen |
| DE4444911A1 (de) | 1994-12-16 | 1996-06-27 | Basf Ag | Fungizide Mischung |
| KR100432453B1 (ko) * | 1996-04-26 | 2005-01-15 | 바스프 악티엔게젤샤프트 | 살진균제 혼합물 |
| NZ332076A (en) * | 1996-04-26 | 2000-02-28 | Basf Ag | Fungicide mixture containing a carbamate derivative and an oxime ether derivative or triazole derivative |
| DE19710760A1 (de) * | 1997-03-14 | 1998-09-17 | Basf Ag | Fungizide Mischung |
| UA68353C2 (ru) * | 1997-06-04 | 2004-08-16 | Басф Акцієнгезелльшафт | Фунгицидная смесь, способ борьбы с фитопатогенными грибами и фунгицидные средства |
| PT1130963E (pt) * | 1998-11-20 | 2005-06-30 | Bayer Cropscience Ag | Combinacoes de substancias activas fungicidas |
| UA72490C2 (ru) * | 1998-12-22 | 2005-03-15 | Басф Акцієнгезелльшафт | Фунгицидная смесь и способ борьбы с фитопатогенными грибами |
-
1999
- 1999-11-12 UA UA2001075221A patent/UA72490C2/ru unknown
- 1999-12-08 TW TW088121485A patent/TW529909B/zh not_active IP Right Cessation
- 1999-12-11 EP EP99963499A patent/EP1139758B1/de not_active Expired - Lifetime
- 1999-12-11 WO PCT/EP1999/009812 patent/WO2000036921A1/de active IP Right Grant
- 1999-12-11 KR KR1020017007918A patent/KR100692507B1/ko not_active IP Right Cessation
- 1999-12-11 JP JP2000589043A patent/JP4570785B2/ja not_active Expired - Fee Related
- 1999-12-11 IL IL14344899A patent/IL143448A0/xx active IP Right Grant
- 1999-12-11 ES ES99963499T patent/ES2198982T3/es not_active Expired - Lifetime
- 1999-12-11 US US09/868,724 patent/US6541500B1/en not_active Expired - Lifetime
- 1999-12-11 DE DE59905365T patent/DE59905365D1/de not_active Expired - Lifetime
- 1999-12-11 PT PT99963499T patent/PT1139758E/pt unknown
- 1999-12-11 AU AU19775/00A patent/AU769532B2/en not_active Expired
- 1999-12-11 CN CNB998149497A patent/CN1293809C/zh not_active Expired - Fee Related
- 1999-12-11 SK SK883-2001A patent/SK284861B6/sk not_active IP Right Cessation
- 1999-12-11 NZ NZ512934A patent/NZ512934A/xx not_active IP Right Cessation
- 1999-12-11 HU HU0104751A patent/HU229238B1/hu not_active IP Right Cessation
- 1999-12-11 PL PL348506A patent/PL198429B1/pl unknown
- 1999-12-11 AT AT99963499T patent/ATE238665T1/de active
- 1999-12-11 CA CA002355711A patent/CA2355711C/en not_active Expired - Fee Related
- 1999-12-11 BR BRPI9916453-1A patent/BR9916453B1/pt not_active IP Right Cessation
- 1999-12-11 DK DK99963499T patent/DK1139758T3/da active
- 1999-12-11 EA EA200100644A patent/EA004293B1/ru not_active IP Right Cessation
- 1999-12-11 CZ CZ20012197A patent/CZ301438B6/cs not_active IP Right Cessation
- 1999-12-16 CO CO99078832A patent/CO5221028A1/es active IP Right Grant
- 1999-12-22 AR ARP990106683A patent/AR021992A1/es active IP Right Grant
-
2001
- 2001-05-30 IL IL143448A patent/IL143448A/en not_active IP Right Cessation
- 2001-07-20 ZA ZA200105979A patent/ZA200105979B/en unknown
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