JP2005520839A5 - - Google Patents
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- Publication number
- JP2005520839A5 JP2005520839A5 JP2003577631A JP2003577631A JP2005520839A5 JP 2005520839 A5 JP2005520839 A5 JP 2005520839A5 JP 2003577631 A JP2003577631 A JP 2003577631A JP 2003577631 A JP2003577631 A JP 2003577631A JP 2005520839 A5 JP2005520839 A5 JP 2005520839A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- halogen
- independently
- alkylsulfinyl
- haloalkoxy
- 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.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 claims description 18
- 229910052736 halogen Inorganic materials 0.000 claims description 18
- 150000002367 halogens Chemical class 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 16
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 14
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 14
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 14
- -1 C 1 -C 4 alkoxy Chemical group 0.000 claims description 14
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims description 12
- 125000001424 substituent group Chemical group 0.000 claims description 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 8
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 8
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 8
- 150000001204 N-oxides Chemical class 0.000 claims description 8
- 230000002538 fungal effect Effects 0.000 claims description 8
- 239000000417 fungicide Substances 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 6
- 125000004473 dialkylaminocarbonyl 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
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 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
- 125000006310 cycloalkyl amino 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
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 150000003432 sterols Chemical class 0.000 claims description 4
- 235000003702 sterols Nutrition 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 230000000855 fungicidal effect Effects 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 2
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 2
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 2
- 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
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 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
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000003899 bactericide agent Substances 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 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
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 2
- 239000000645 desinfectant Substances 0.000 claims description 2
- 239000012990 dithiocarbamate Substances 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 230000002438 mitochondrial effect Effects 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 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
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 125000004665 trialkylsilyl group Chemical group 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 description 4
- 0 CC[C@](C(*)C(CCC[C@](*C)*(CC)=*)CC(C)CCC(*)CC(C)C(C)C1=*C1)C=CCCCC1C*CCC1 Chemical compound CC[C@](C(*)C(CCC[C@](*C)*(CC)=*)CC(C)CCC(*)CC(C)C(C)C1=*C1)C=CCCCC1C*CCC1 0.000 description 2
- 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
- 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 |
|---|---|---|---|
| US36576402P | 2002-03-19 | 2002-03-19 | |
| PCT/US2003/008205 WO2003079788A2 (en) | 2002-03-19 | 2003-03-18 | Benzamides and compositions benzamides for use as fungizide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005520839A JP2005520839A (ja) | 2005-07-14 |
| JP2005520839A5 true JP2005520839A5 (enExample) | 2006-05-11 |
Family
ID=28454711
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003577631A Pending JP2005520839A (ja) | 2002-03-19 | 2003-03-18 | 殺菌・殺カビ剤として使用するためのベンズアミドおよびベンズアミド組成物 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US20050164999A1 (enExample) |
| EP (5) | EP2260703A3 (enExample) |
| JP (1) | JP2005520839A (enExample) |
| CN (2) | CN1642421A (enExample) |
| AR (1) | AR039029A1 (enExample) |
| AU (1) | AU2003220361A1 (enExample) |
| BR (1) | BR0308457B1 (enExample) |
| DK (1) | DK1484970T3 (enExample) |
| ES (1) | ES2425941T3 (enExample) |
| IL (1) | IL162895A0 (enExample) |
| MX (1) | MXPA04009001A (enExample) |
| MY (1) | MY138071A (enExample) |
| PL (3) | PL211319B1 (enExample) |
| PT (1) | PT1484970E (enExample) |
| RU (2) | RU2483540C2 (enExample) |
| SI (1) | SI1484970T1 (enExample) |
| TW (1) | TW200306155A (enExample) |
| WO (1) | WO2003079788A2 (enExample) |
| ZA (1) | ZA200405644B (enExample) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2821719B1 (fr) | 2001-03-08 | 2003-06-13 | Aventis Cropscience Sa | Nouvelles compositions fongicides a base de derive de pyridylmethylbenzamide et de propamocarbe |
| FR2821720B1 (fr) | 2001-03-08 | 2003-06-13 | Aventis Cropscience Sa | Compositions fongicides comprenant notamment un derive de pyridylmethylbenzamide |
| FR2831022B1 (fr) | 2001-10-23 | 2004-01-23 | Aventis Cropscience Sa | Composition fongicide a base d'au moins un derive de pyridylmethylbenzamide et d'au moins un derive dithiocarbamate |
| 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 |
| JP4570615B2 (ja) | 2003-04-15 | 2010-10-27 | バイエル・クロツプサイエンス・エス・アー | ピリジルメチルベンズアミド誘導体とクロロタロニルを含有してなる殺菌剤組成物 |
| EP1604571A1 (en) * | 2004-04-06 | 2005-12-14 | Bayer CropScience S.A. | Fungicidal composition comprising a pyridylmethylbenzamide derivative and a quinone derivative |
| WO2006008192A1 (en) * | 2004-07-23 | 2006-01-26 | Bayer Cropscience Sa | N-[2-(4-pyridinyl)ethyl]benzamide derivatives as fungicides |
| KR20130089671A (ko) * | 2005-02-11 | 2013-08-12 | 바이엘 크롭사이언스 아게 | 피리딜메틸벤즈아미드 유도체 및 티아졸카르복사미드 유도체를 포함하는 살진균성 조성물 |
| TWI435863B (zh) * | 2006-03-20 | 2014-05-01 | Nihon Nohyaku Co Ltd | Ｎ-２-（雜）芳基乙基甲醯胺衍生物及含該衍生物之蟲害防治劑 |
| JP5592894B2 (ja) * | 2008-12-02 | 2014-09-17 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 殺真菌性複素環化合物 |
| US20130102477A1 (en) | 2010-06-23 | 2013-04-25 | Ryan D. Morin | Biomarkers for non-hodgkin lymphomas and uses thereof |
| JP6389036B2 (ja) | 2010-09-10 | 2018-09-12 | エピザイム インコーポレイテッド | ヒトｅｚｈ２の阻害剤、およびその使用方法 |
| US9175331B2 (en) | 2010-09-10 | 2015-11-03 | Epizyme, Inc. | Inhibitors of human EZH2, and methods of use thereof |
| EP3295797A1 (en) * | 2011-03-23 | 2018-03-21 | Bayer Intellectual Property GmbH | Active compound combinations |
| TW201733984A (zh) | 2011-04-13 | 2017-10-01 | 雅酶股份有限公司 | 經取代之苯化合物 |
| JO3438B1 (ar) | 2011-04-13 | 2019-10-20 | Epizyme Inc | مركبات بنزين مستبدلة بأريل أو أريل غير متجانس |
| CN102626097A (zh) * | 2012-03-28 | 2012-08-08 | 陕西上格之路生物科学有限公司 | 一种含噁唑菌酮的杀菌组合物 |
| PL3184523T3 (pl) | 2012-04-13 | 2019-12-31 | Epizyme Inc | Bromowodorek N-((4,6-dimetylo-2-okso-1,2-dihydropirydyn-3-ylo)metylo)-5- (etylo(tetrahydro-2H-piran-4-ylo)amino)-4-metylo-4'-(morfolinometylo)-[1,1'- bifenylo]-3-karboksyamidu do zastosowania w leczeniu zaburzenia proliferacji komórkowej układu hematologicznego |
| KR20150013690A (ko) * | 2012-05-07 | 2015-02-05 | 다우 아그로사이언시즈 엘엘씨 | 살진균제로서 매크로사이클 피콜린아미드 |
| SG10201705989YA (en) | 2012-10-15 | 2017-08-30 | Epizyme Inc | Substituted benzene compounds |
| EP4324525A3 (en) | 2013-10-16 | 2024-07-17 | Epizyme, Inc. | Hydrochloride salt form for ezh2 inhibition |
| RU2550494C1 (ru) * | 2013-12-04 | 2015-05-10 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Тихоокеанский государственный университет" | Минеральное удобрение |
| US9877486B2 (en) | 2014-01-31 | 2018-01-30 | AgBiome, Inc. | Methods of growing plants using modified biological control agents |
| PL3099172T3 (pl) | 2014-01-31 | 2022-01-24 | AgBiome, Inc. | Zmodyfikowany środek do zwalczania biologicznego i jego zastosowania |
| RU2581929C2 (ru) * | 2014-05-07 | 2016-04-20 | Общество с ограниченной ответственностью "ФУНГИПАК" | Биологически-активный препарат для защиты растений от вредителей, способ его получения, микроконтейнер для названного препарата, способ его изготовления и способ защиты растений от вредителей |
| ES2841373T3 (es) | 2015-08-17 | 2021-07-08 | Obshchestvo S Ogranitchennoy Otvetstvennostyu Fungi Pak | Preparación biológicamente activa que comprende microcontenedores para proteger plantas contra plagas y método para su producción |
| US12084472B2 (en) | 2015-12-18 | 2024-09-10 | Ardelyx, Inc. | Substituted 4-phenyl pyridine compounds as non-systemic TGR5 agonists |
| TW202246215A (zh) | 2015-12-18 | 2022-12-01 | 美商亞德利克斯公司 | 作為非全身ｔｇｒ５促效劑之經取代之４－苯基吡啶化合物 |
| RU2728697C1 (ru) * | 2019-12-24 | 2020-07-30 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Московский государственный университет имени М.В. Ломоносова" (МГУ) | Сорбционно-стимулирующий препарат для предпосевной обработки семян яровой пшеницы на основе полиэтиленгликоля |
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| 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 |
| FR2821720B1 (fr) * | 2001-03-08 | 2003-06-13 | Aventis Cropscience Sa | Compositions fongicides comprenant notamment un derive de pyridylmethylbenzamide |
| FR2831022B1 (fr) * | 2001-10-23 | 2004-01-23 | Aventis Cropscience Sa | Composition fongicide a base d'au moins un derive de pyridylmethylbenzamide et d'au moins un derive dithiocarbamate |
| 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 |
| TW200407075A (en) * | 2002-03-19 | 2004-05-16 | Du Pont | Pyridinyl amides and advantageous compositions thereof for use as fungicides |
| TW200306782A (en) * | 2002-03-19 | 2003-12-01 | Du Pont | Pyridinyl amides and advantageous compositions thereof for use as fungicides |
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2003
- 2003-02-19 TW TW092103416A patent/TW200306155A/zh unknown
- 2003-03-18 PL PL390541A patent/PL211319B1/pl not_active IP Right Cessation
- 2003-03-18 EP EP10010398A patent/EP2260703A3/en not_active Withdrawn
- 2003-03-18 PT PT37166618T patent/PT1484970E/pt unknown
- 2003-03-18 WO PCT/US2003/008205 patent/WO2003079788A2/en not_active Ceased
- 2003-03-18 PL PL393150A patent/PL393150A1/pl not_active Application Discontinuation
- 2003-03-18 US US10/501,126 patent/US20050164999A1/en not_active Abandoned
- 2003-03-18 EP EP10010401A patent/EP2260705A3/en not_active Withdrawn
- 2003-03-18 RU RU2007128523/13A patent/RU2483540C2/ru not_active IP Right Cessation
- 2003-03-18 MX MXPA04009001A patent/MXPA04009001A/es active IP Right Grant
- 2003-03-18 CN CNA038064545A patent/CN1642421A/zh active Pending
- 2003-03-18 MY MYPI20030951A patent/MY138071A/en unknown
- 2003-03-18 EP EP03716661.8A patent/EP1484970B1/en not_active Expired - Lifetime
- 2003-03-18 AU AU2003220361A patent/AU2003220361A1/en not_active Abandoned
- 2003-03-18 RU RU2004130840/04A patent/RU2314690C2/ru not_active IP Right Cessation
- 2003-03-18 JP JP2003577631A patent/JP2005520839A/ja active Pending
- 2003-03-18 BR BRPI0308457-4A patent/BR0308457B1/pt not_active IP Right Cessation
- 2003-03-18 DK DK03716661.8T patent/DK1484970T3/da active
- 2003-03-18 IL IL16289503A patent/IL162895A0/xx unknown
- 2003-03-18 CN CN201010158667A patent/CN101803609A/zh active Pending
- 2003-03-18 PL PL03372885A patent/PL372885A1/xx not_active Application Discontinuation
- 2003-03-18 ES ES03716661T patent/ES2425941T3/es not_active Expired - Lifetime
- 2003-03-18 SI SI200332299T patent/SI1484970T1/sl unknown
- 2003-03-18 EP EP10010399A patent/EP2258190A3/en not_active Withdrawn
- 2003-03-18 EP EP10010400.9A patent/EP2260704B1/en not_active Expired - Lifetime
- 2003-03-19 AR ARP030100970A patent/AR039029A1/es unknown
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2004
- 2004-07-15 ZA ZA2004/05644A patent/ZA200405644B/en unknown
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