CA2551148C - Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the methionine biosynthesis - Google Patents
Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the methionine biosynthesis Download PDFInfo
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- CA2551148C CA2551148C CA2551148A CA2551148A CA2551148C CA 2551148 C CA2551148 C CA 2551148C CA 2551148 A CA2551148 A CA 2551148A CA 2551148 A CA2551148 A CA 2551148A CA 2551148 C CA2551148 C CA 2551148C
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- trifluoromethyl
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- 239000000203 mixture Substances 0.000 title claims abstract description 70
- 150000001875 compounds Chemical class 0.000 title claims abstract description 28
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 17
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 title claims abstract description 10
- 230000015572 biosynthetic process Effects 0.000 title claims abstract description 10
- 230000002401 inhibitory effect Effects 0.000 title claims abstract description 10
- 229930182817 methionine Natural products 0.000 title claims abstract description 10
- 238000000034 method Methods 0.000 claims abstract description 14
- 241000233866 Fungi Species 0.000 claims abstract description 8
- 230000003032 phytopathogenic effect Effects 0.000 claims abstract description 6
- -1 amino, phenoxy Chemical group 0.000 claims description 12
- 239000005805 Mepanipyrim Substances 0.000 claims description 10
- 239000005828 Pyrimethanil Substances 0.000 claims description 10
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- CIFWZNRJIBNXRE-UHFFFAOYSA-N mepanipyrim Chemical compound CC#CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 CIFWZNRJIBNXRE-UHFFFAOYSA-N 0.000 claims description 9
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 claims description 9
- 125000001188 haloalkyl group Chemical group 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
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- 125000000217 alkyl group Chemical group 0.000 claims description 6
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- 125000001424 substituent group Chemical group 0.000 claims description 4
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- 239000005867 Iprodione Substances 0.000 claims description 3
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- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 claims description 3
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 claims description 3
- 231100001184 nonphytotoxic Toxicity 0.000 claims description 3
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 claims description 3
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 claims description 3
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 claims description 3
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- 150000001204 N-oxides Chemical class 0.000 claims description 2
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- 125000002252 acyl group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000005082 alkoxyalkenyl group Chemical group 0.000 claims description 2
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
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- 125000004422 alkyl sulphonamide group Chemical group 0.000 claims 1
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- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 description 1
- JPFWJDMDPLEUBD-ITJAGOAWSA-N polyoxorim Polymers O[C@@H]1[C@H](O)[C@@H]([C@H](NC(=O)[C@H]([C@H](O)[C@@H](O)COC(N)=O)N)C(O)=O)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-ITJAGOAWSA-N 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 229940050982 potassium hydroxyquinoline sulfate Drugs 0.000 description 1
- DWBSXHMYTSZXQL-UHFFFAOYSA-M potassium;quinolin-8-yl sulfate Chemical compound [K+].C1=CN=C2C(OS(=O)(=O)[O-])=CC=CC2=C1 DWBSXHMYTSZXQL-UHFFFAOYSA-M 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000004493 powder for dry seed treatment Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 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
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 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
- FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 description 1
- JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 description 1
- VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-UHFFFAOYSA-N 0.000 description 1
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 1
- MRUMAIRJPMUAPZ-UHFFFAOYSA-N quinolin-8-ol;sulfuric acid Chemical compound OS(O)(=O)=O.C1=CN=C2C(O)=CC=CC2=C1 MRUMAIRJPMUAPZ-UHFFFAOYSA-N 0.000 description 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 1
- WRPIRSINYZBGPK-UHFFFAOYSA-N quinoxyfen Chemical compound C1=CC(F)=CC=C1OC1=CC=NC2=CC(Cl)=CC(Cl)=C12 WRPIRSINYZBGPK-UHFFFAOYSA-N 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 239000004542 seed coated with a pesticide Substances 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- MXMXHPPIGKYTAR-UHFFFAOYSA-N silthiofam Chemical compound CC=1SC([Si](C)(C)C)=C(C(=O)NCC=C)C=1C MXMXHPPIGKYTAR-UHFFFAOYSA-N 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- HCJLVWUMMKIQIM-UHFFFAOYSA-M sodium;2,3,4,5,6-pentachlorophenolate Chemical compound [Na+].[O-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl HCJLVWUMMKIQIM-UHFFFAOYSA-M 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000004528 solution for seed treatment Substances 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000002641 tar oil Substances 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- WOSNCVAPUOFXEH-UHFFFAOYSA-N thifluzamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=C(Br)C=C(OC(F)(F)F)C=C1Br WOSNCVAPUOFXEH-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 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
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 239000004560 ultra-low volume (ULV) liquid Substances 0.000 description 1
- 239000004555 ultra-low volume (ULV) suspension Substances 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004564 water dispersible powder for slurry treatment Substances 0.000 description 1
- 239000004565 water dispersible tablet Substances 0.000 description 1
- 239000004553 water soluble powder for seed treatment Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 241000228158 x Triticosecale Species 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
- A01N43/34—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
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05G—MIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
- C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
- C05G3/60—Biocides or preservatives, e.g. disinfectants, pesticides or herbicides; Pest repellants or attractants
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agronomy & Crop Science (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)
- Pyridine Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04356015.0 | 2004-02-12 | ||
| EP04356015A EP1570737A1 (en) | 2004-02-12 | 2004-02-12 | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the methionine biosynthesis |
| US63699904P | 2004-12-17 | 2004-12-17 | |
| US60/636,999 | 2004-12-17 | ||
| PCT/EP2005/002567 WO2005077182A1 (en) | 2004-02-12 | 2005-02-10 | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the methionine biosynthesis |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2551148A1 CA2551148A1 (en) | 2005-08-25 |
| CA2551148C true CA2551148C (en) | 2012-08-21 |
Family
ID=34746176
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2551148A Expired - Lifetime CA2551148C (en) | 2004-02-12 | 2005-02-10 | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the methionine biosynthesis |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US8410020B2 (enExample) |
| EP (2) | EP1570737A1 (enExample) |
| JP (1) | JP4686483B2 (enExample) |
| CN (1) | CN1917761B (enExample) |
| AT (1) | ATE406097T1 (enExample) |
| AU (1) | AU2005213185B2 (enExample) |
| BR (1) | BRPI0506619B1 (enExample) |
| CA (1) | CA2551148C (enExample) |
| DK (1) | DK1713335T3 (enExample) |
| ES (1) | ES2313306T3 (enExample) |
| NZ (1) | NZ548020A (enExample) |
| PL (1) | PL1713335T3 (enExample) |
| PT (1) | PT1713335E (enExample) |
| RU (1) | RU2359456C2 (enExample) |
| SI (1) | SI1713335T1 (enExample) |
| UA (1) | UA80378C2 (enExample) |
| WO (1) | WO2005077182A1 (enExample) |
| ZA (1) | ZA200606378B (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1563731A1 (en) | 2004-02-12 | 2005-08-17 | Bayer CropScience S.A. | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the ergosterol biosynthesis |
| UA86652C2 (ru) * | 2004-10-22 | 2009-05-12 | Янссен Фармацевтика Н.В. | Применение анилинопиримидина для защиты древесины и способ защиты древесины или изделий из древесины от грибков |
| ES2385073T3 (es) * | 2005-09-29 | 2012-07-17 | Syngenta Participations Ag | Composiciones fungicidas |
| JP5466503B2 (ja) * | 2006-07-06 | 2014-04-09 | バイエル・クロップサイエンス・アーゲー | ピリジルエチルベンズアミド誘導体及び殺虫性化合物を含んでいる殺有害生物剤組成物 |
| US20120010253A1 (en) | 2009-03-16 | 2012-01-12 | Basf Se | Fungicidal compositions comprising Fluopyram and Metrafenone |
| CN103535355A (zh) * | 2012-07-13 | 2014-01-29 | 陕西美邦农药有限公司 | 一种高效杀菌组合物 |
| CN104285954B (zh) * | 2012-07-13 | 2016-08-24 | 陕西美邦农药有限公司 | 一种杀菌组合物 |
| CN106857534A (zh) * | 2017-03-23 | 2017-06-20 | 陕西上格之路生物科学有限公司 | 一种含有氟吡菌酰胺和嘧霉胺的杀菌组合物 |
| WO2020231751A1 (en) | 2019-05-10 | 2020-11-19 | Bayer Cropscience Lp | Active compound combinations |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5153200A (en) * | 1987-09-28 | 1992-10-06 | Ciba-Geigy Corporation | Pesticides |
| GB8820231D0 (en) | 1988-08-25 | 1988-09-28 | Fujisawa Pharmaceutical Co | New benzazole compounds processes for preparation thereof & pharmaceutical composition comprising same |
| DE4318372B4 (de) * | 1992-06-10 | 2010-10-28 | BASF Agro B.V., Arnhem (NL)-Wädenswil-Branch | Fungizide Mischungen |
| GB2267644B (en) * | 1992-06-10 | 1996-02-07 | Schering Ag | Fungicidal mixtures |
| TW575562B (en) | 1998-02-19 | 2004-02-11 | Agrevo Uk Ltd | Fungicides |
| JP4259678B2 (ja) | 1999-03-24 | 2009-04-30 | 日本曹達株式会社 | 農園芸用有害生物防除組成物 |
| PT1204323E (pt) * | 1999-08-18 | 2004-11-30 | Aventis Cropscience Gmbh | Fungicidas |
| EP1256569B1 (en) * | 2000-02-16 | 2010-07-07 | Ishihara Sangyo Kaisha, Ltd. | Phenacylamine derivatives, production thereof and pest controllers containing the derivatives |
| FR2821718B1 (fr) | 2001-03-08 | 2003-06-13 | Aventis Cropscience Sa | Nouvelles compositions fongicides a base de derives de pyridylmethylbenzamide et d'imidazoline ou d'oxazolidine |
| MXPA04002176A (es) * | 2001-09-07 | 2004-06-29 | Syngenta Participations Ag | Sistemas surfactantes para compuestos agricolamente activos. |
| FR2832031A1 (fr) * | 2001-11-14 | 2003-05-16 | Aventis Cropscience Sa | Composition fongicide a base d'au moins un derive de pyridylmethylbenzamide et d'au moins un derive de type valinamide |
| PL222168B1 (pl) * | 2002-08-12 | 2016-07-29 | Bayer Cropscience Sa | Pochodne 2-pirydyloetylobenzamidu zawierająca je kompozycja grzybobójcza i sposób zapobiegawczego lub kuracyjnego zwalczania chorobotwórczych grzybów roślin w uprawach |
| EP1563731A1 (en) * | 2004-02-12 | 2005-08-17 | Bayer CropScience S.A. | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the ergosterol biosynthesis |
| EP1570738A1 (en) * | 2004-02-12 | 2005-09-07 | Bayer CropScience S.A. | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the spores germination or mycelium growth by acting on different metabolic routes |
-
2004
- 2004-02-12 EP EP04356015A patent/EP1570737A1/en not_active Withdrawn
-
2005
- 2005-02-10 EP EP05715941A patent/EP1713335B1/en not_active Expired - Lifetime
- 2005-02-10 AT AT05715941T patent/ATE406097T1/de active
- 2005-02-10 RU RU2006132504/04A patent/RU2359456C2/ru active
- 2005-02-10 SI SI200530461T patent/SI1713335T1/sl unknown
- 2005-02-10 NZ NZ548020A patent/NZ548020A/en not_active IP Right Cessation
- 2005-02-10 ES ES05715941T patent/ES2313306T3/es not_active Expired - Lifetime
- 2005-02-10 AU AU2005213185A patent/AU2005213185B2/en not_active Expired
- 2005-02-10 BR BRPI0506619-0A patent/BRPI0506619B1/pt not_active IP Right Cessation
- 2005-02-10 PL PL05715941T patent/PL1713335T3/pl unknown
- 2005-02-10 CA CA2551148A patent/CA2551148C/en not_active Expired - Lifetime
- 2005-02-10 JP JP2006552586A patent/JP4686483B2/ja not_active Expired - Lifetime
- 2005-02-10 DK DK05715941T patent/DK1713335T3/da active
- 2005-02-10 WO PCT/EP2005/002567 patent/WO2005077182A1/en not_active Ceased
- 2005-02-10 PT PT05715941T patent/PT1713335E/pt unknown
- 2005-02-10 US US10/588,360 patent/US8410020B2/en active Active
- 2005-02-10 CN CN2005800042179A patent/CN1917761B/zh not_active Expired - Lifetime
- 2005-10-02 UA UAA200609673A patent/UA80378C2/uk unknown
-
2006
- 2006-08-01 ZA ZA200606378A patent/ZA200606378B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US8410020B2 (en) | 2013-04-02 |
| AU2005213185A1 (en) | 2005-08-25 |
| UA80378C2 (en) | 2007-09-10 |
| DK1713335T3 (da) | 2009-01-12 |
| CN1917761B (zh) | 2010-05-26 |
| ES2313306T3 (es) | 2009-03-01 |
| WO2005077182A1 (en) | 2005-08-25 |
| NZ548020A (en) | 2010-09-30 |
| ATE406097T1 (de) | 2008-09-15 |
| EP1713335A1 (en) | 2006-10-25 |
| CA2551148A1 (en) | 2005-08-25 |
| PL1713335T3 (pl) | 2009-02-27 |
| BRPI0506619B1 (pt) | 2015-08-04 |
| RU2006132504A (ru) | 2008-03-20 |
| RU2359456C2 (ru) | 2009-06-27 |
| PT1713335E (pt) | 2008-11-17 |
| CN1917761A (zh) | 2007-02-21 |
| EP1570737A1 (en) | 2005-09-07 |
| SI1713335T1 (sl) | 2009-02-28 |
| EP1713335B1 (en) | 2008-08-27 |
| JP4686483B2 (ja) | 2011-05-25 |
| AU2005213185B2 (en) | 2010-09-16 |
| ZA200606378B (en) | 2008-07-30 |
| BRPI0506619A (pt) | 2007-05-02 |
| US20070137273A1 (en) | 2007-06-21 |
| JP2007522186A (ja) | 2007-08-09 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |