JP2005520838A5 - - Google Patents
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- Publication number
- JP2005520838A5 JP2005520838A5 JP2003577630A JP2003577630A JP2005520838A5 JP 2005520838 A5 JP2005520838 A5 JP 2005520838A5 JP 2003577630 A JP2003577630 A JP 2003577630A JP 2003577630 A JP2003577630 A JP 2003577630A JP 2005520838 A5 JP2005520838 A5 JP 2005520838A5
- Authority
- JP
- Japan
- Prior art keywords
- component
- fungal
- plant
- composition according
- independently
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 claims description 20
- 150000001875 compounds Chemical class 0.000 claims description 18
- -1 C 1 -C 4 alkoxy Chemical group 0.000 claims description 8
- 230000002538 fungal effect Effects 0.000 claims description 8
- 239000000417 fungicide Substances 0.000 claims description 8
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 6
- 201000010099 disease Diseases 0.000 claims description 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 4
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 4
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 4
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims description 4
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 4
- 229930182558 Sterol Natural products 0.000 claims description 4
- 230000006696 biosynthetic metabolic pathway Effects 0.000 claims description 4
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 4
- 230000006315 carbonylation Effects 0.000 claims description 4
- 238000005810 carbonylation reaction Methods 0.000 claims description 4
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 4
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims description 4
- 244000053095 fungal pathogen Species 0.000 claims description 4
- 244000000004 fungal plant pathogen Species 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 150000003432 sterols Chemical class 0.000 claims description 4
- 235000003702 sterols Nutrition 0.000 claims description 4
- 230000000855 fungicidal effect Effects 0.000 claims description 3
- YCIPQJTZJGUXND-UHFFFAOYSA-N Aglaia odorata Alkaloid Natural products C1=CC(OC)=CC=C1C1(C(C=2C(=O)N3CCCC3=NC=22)C=3C=CC=CC=3)C2(O)C2=C(OC)C=C(OC)C=C2O1 YCIPQJTZJGUXND-UHFFFAOYSA-N 0.000 claims description 2
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 2
- 102000004190 Enzymes Human genes 0.000 claims description 2
- 108090000790 Enzymes Proteins 0.000 claims description 2
- 101000615488 Homo sapiens Methyl-CpG-binding domain protein 2 Proteins 0.000 claims description 2
- 102100021299 Methyl-CpG-binding domain protein 2 Human genes 0.000 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 230000000844 anti-bacterial effect Effects 0.000 claims description 2
- 239000003899 bactericide agent Substances 0.000 claims description 2
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 claims description 2
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 claims description 2
- 239000000645 desinfectant Substances 0.000 claims description 2
- 239000012990 dithiocarbamate Substances 0.000 claims description 2
- 230000002438 mitochondrial effect Effects 0.000 claims description 2
- 125000005543 phthalimide group Chemical class 0.000 claims description 2
- 150000003053 piperidines Chemical class 0.000 claims description 2
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical compound OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 claims description 2
- 230000000241 respiratory effect Effects 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 description 4
- 241000233866 Fungi Species 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 description 1
- 239000005772 Famoxadone Substances 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 239000005802 Mancozeb Substances 0.000 description 1
- 241000233654 Oomycetes Species 0.000 description 1
- 241000233614 Phytophthora Species 0.000 description 1
- 241000233622 Phytophthora infestans Species 0.000 description 1
- 241000233626 Plasmopara Species 0.000 description 1
- 241001281803 Plasmopara viticola Species 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36576602P | 2002-03-19 | 2002-03-19 | |
| PCT/US2003/008186 WO2003079787A1 (en) | 2002-03-19 | 2003-03-18 | Synergistic fungicide compositions containing at least one n-`(2-pyridinyl)methyl!-3-pyridinecarboxamide derivative and one or more further fungicides useful for controlling fungal plant diseases |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005520838A JP2005520838A (ja) | 2005-07-14 |
| JP2005520838A5 true JP2005520838A5 (enExample) | 2006-05-11 |
Family
ID=28454713
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003577630A Withdrawn JP2005520838A (ja) | 2002-03-19 | 2003-03-18 | 菌・カビ性植物病害を防御するために有用な、少なくとも１つのｎ’−（２−ピリジニル）メチル−３−ピリジンカルボキサミド誘導体と、１つもしくはそれ以上の更なる殺菌・殺カビ剤とを含有する相乗的殺菌・殺カビ剤組成物 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US20050009889A1 (enExample) |
| EP (1) | EP1484969A1 (enExample) |
| JP (1) | JP2005520838A (enExample) |
| CN (1) | CN1665395A (enExample) |
| AR (1) | AR039030A1 (enExample) |
| AU (1) | AU2003220358A1 (enExample) |
| BR (1) | BR0308459A (enExample) |
| IL (1) | IL162894A0 (enExample) |
| MX (1) | MXPA04009000A (enExample) |
| PL (1) | PL372569A1 (enExample) |
| RU (1) | RU2004130839A (enExample) |
| TW (1) | TW200407075A (enExample) |
| WO (1) | WO2003079787A1 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200306155A (en) * | 2002-03-19 | 2003-11-16 | Du Pont | Benzamides and advantageous compositions thereof for use as fungicides |
| DE10248335A1 (de) | 2002-10-17 | 2004-05-06 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| FR2928070A1 (fr) * | 2008-02-27 | 2009-09-04 | Sumitomo Chemical Co | Composition agricole, utilisation d'un compose pour sa production et procede pour matriser ou prevenir les maladies des plantes. |
| US9302991B2 (en) * | 2010-10-18 | 2016-04-05 | Raqualia Pharma Inc. | Arylamide derivatives as TTX-S blockers |
| CN102084865B (zh) * | 2011-03-25 | 2013-10-30 | 陕西先农生物科技有限公司 | 粉唑醇·丙森锌杀菌组合物 |
| JP2017206440A (ja) * | 2014-09-10 | 2017-11-24 | 日本曹達株式会社 | ピリジン化合物およびその用途 |
| US12376898B2 (en) | 2016-07-01 | 2025-08-05 | Cynosure, Llc | Non-invasive, uniform and non-uniform RF methods and systems related applications |
| BR112021006225A2 (pt) * | 2018-10-02 | 2021-07-06 | Syngenta Participations Ag | compostos de benzeno- e azina-amida ativos em termos pesticidas |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0710841A (ja) * | 1993-06-21 | 1995-01-13 | Ishihara Sangyo Kaisha Ltd | ４−トリフルオロメチルピリジン−３−カルボキサミド系化合物又はその塩、それらの製造方法及びそれらを含有する有害動物防除剤 |
| JPH0725853A (ja) * | 1993-07-14 | 1995-01-27 | Ishihara Sangyo Kaisha Ltd | アミド系化合物又はその塩、それらの製造方法及びそれらを含有する有害動物防除剤 |
| UA65600C2 (uk) * | 1997-12-18 | 2004-04-15 | Басф Акцієнгезелльшафт | Фунгіцидна суміш на основі амідних сполук і похідних піридину |
| GB9919588D0 (en) * | 1999-08-18 | 1999-10-20 | Hoechst Schering Agrevo Gmbh | Fungicidal compounds |
| EP1322614A2 (en) * | 2000-09-18 | 2003-07-02 | E. I. du Pont de Nemours and Company | Pyridinyl amides and imides for use as fungicides |
| TW200306159A (en) * | 2002-03-19 | 2003-11-16 | Du Pont | Bicyclic fused pyridinyl amides and advantageous compositions thereof for use as fungicides |
-
2003
- 2003-02-27 TW TW092104247A patent/TW200407075A/zh unknown
- 2003-03-18 EP EP03716658A patent/EP1484969A1/en not_active Withdrawn
- 2003-03-18 MX MXPA04009000A patent/MXPA04009000A/es unknown
- 2003-03-18 US US10/501,853 patent/US20050009889A1/en not_active Abandoned
- 2003-03-18 IL IL16289403A patent/IL162894A0/xx unknown
- 2003-03-18 PL PL03372569A patent/PL372569A1/xx not_active Application Discontinuation
- 2003-03-18 WO PCT/US2003/008186 patent/WO2003079787A1/en not_active Ceased
- 2003-03-18 AU AU2003220358A patent/AU2003220358A1/en not_active Abandoned
- 2003-03-18 RU RU2004130839/04A patent/RU2004130839A/ru not_active Application Discontinuation
- 2003-03-18 CN CN03806453.7A patent/CN1665395A/zh active Pending
- 2003-03-18 JP JP2003577630A patent/JP2005520838A/ja not_active Withdrawn
- 2003-03-18 BR BR0308459-0A patent/BR0308459A/pt not_active IP Right Cessation
- 2003-03-19 AR ARP030100971A patent/AR039030A1/es not_active Application Discontinuation
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