专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

1. 发明授权

US09795140B2 Molecules having pesticidal utility, and intermediates, compositions, and processes, related thereto 有权
公开(公告)号：US09795140B2
公开(公告)日：2017-10-24
申请号：US15092646
申请日：2016-04-07
申请人： Dow AgroSciences LLC
发明人： Timothy P. Martin , Joseph D. Eckelbarger , Ronald Ross, Jr. , Kyle DeKorver , Ronald J. Heemstra , Daniel I. Knueppel , Peter Vednor , Ricky Hunter , David A. Demeter , Tony K. Trullinger , Erich Baum , Zoltan Benko , Nakyen Choy , Gary Crouse , John F. Daeuble, Sr. , Fangzheng Li , Jeff Nissen , Michelle Riener , Tom Sparks , Frank Wessels , Maurice Yap
IPC分类号： A01N53/00 , A01N43/90 , C07D207/273 , A01N43/82 , C07D307/33 , C07D277/36 , C07D263/26 , C07D261/12 , C07D333/48 , C07D307/52 , C07D277/30 , C07D213/56 , C07C237/22 , C07D333/60 , C07D233/80 , C07D487/04 , A01N43/707 , A01N43/653 , A01N43/60 , A01N43/40 , A01N41/10 , A01N37/34 , A01N37/22 , C07D253/07 , C07D241/20 , C07C317/14 , C07C233/65 , C07C233/63 , C07D209/49 , C07C381/10 , C07D205/04 , C07C237/42 , C07D207/10 , C07D207/452 , C07C255/29 , C07C255/57 , C07D285/06 , C07D295/32 , C07D305/08 , C07C255/46 , C07D213/75 , C07C255/60 , C07C259/10 , C07D213/81 , C07D213/84 , C07D309/14 , C07D213/89 , C07D215/227 , C07C271/28 , C07C271/66 , C07D231/12 , C07D331/04 , C07D231/56 , C07D333/36 , C07D233/36 , C07C311/08 , C07C311/46 , C07D235/30 , C07C317/28 , C07C317/40 , C07C317/50 , C07C323/41 , C07C323/42 , C07C323/59 , C07D249/08 , C07C331/12 , C07D215/38
CPC分类号： A01N53/00 , A01N37/22 , A01N37/34 , A01N41/10 , A01N43/40 , A01N43/60 , A01N43/653 , A01N43/707 , A01N43/82 , A01N43/90 , C07C233/63 , C07C233/65 , C07C237/22 , C07C237/42 , C07C255/29 , C07C255/46 , C07C255/57 , C07C255/60 , C07C259/10 , C07C271/28 , C07C271/66 , C07C311/08 , C07C311/46 , C07C317/14 , C07C317/28 , C07C317/40 , C07C317/50 , C07C323/41 , C07C323/42 , C07C323/59 , C07C331/12 , C07C381/10 , C07C2601/02 , C07C2601/04 , C07C2601/08 , C07C2601/14 , C07D205/04 , C07D207/10 , C07D207/273 , C07D207/452 , C07D209/49 , C07D213/56 , C07D213/75 , C07D213/81 , C07D213/84 , C07D213/89 , C07D215/227 , C07D215/38 , C07D231/12 , C07D231/56 , C07D233/36 , C07D233/80 , C07D235/30 , C07D241/20 , C07D249/08 , C07D253/07 , C07D261/12 , C07D263/26 , C07D277/30 , C07D277/36 , C07D285/06 , C07D295/32 , C07D305/08 , C07D307/33 , C07D307/52 , C07D309/14 , C07D331/04 , C07D333/36 , C07D333/48 , C07D333/60 , C07D487/04
摘要： This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, pesticidal compositions containing such molecules, and processes of using such pesticidal compositions against such pests. These pesticidal compositions may be used, for example, as acaricides, insecticides, miticides, molluscicides, and nematicides. This document discloses molecules having the following formula (“Formula One”).

2. 发明申请

US20170065565A1 ISOXAZOLINE-SUBSTITUTED BENZAMIDE COMPOUND AND PESTICIDE 审中-公开
标题翻译： ISOXAZOLINE-替代苄基化合物和杀虫剂
公开(公告)号：US20170065565A1
公开(公告)日：2017-03-09
申请号：US15097002
申请日：2016-04-12
申请人： NISSAN CHEMICAL INDUSTRIES, LTD.
发明人： Takeshi Mita , Takamasa KIKUCHI , Takashi MIZUKOSHI , Manabu YAOSAKA , Mitsuaki KOMODA
IPC分类号： A61K31/421 , A61K9/00
CPC分类号： A61K31/421 , A01N43/80 , A61K9/0053 , C07C25/02 , C07C25/06 , C07C25/08 , C07C25/13 , C07C25/24 , C07C43/1742 , C07C43/1745 , C07C205/11 , C07C205/12 , C07C211/52 , C07C251/48 , C07C255/29 , C07C255/50 , C07C255/60 , C07C281/02 , C07C323/09 , C07D261/04 , C07D261/16 , C07D413/04 , C07D413/06 , C07D413/12 , C07D413/14 , C07D417/06 , C07D417/12 , C07F7/0812
摘要： A substituted alkenylbenzene compound of formula (4): wherein X1 is selected from the group consisting of halogen atom, —SF5, C1-C6halo alkyl, hydroxy C1-C6haloalkyl, C1-C6alkoxy C1-C6haloalkyl, C3-C8halocycloalkyl, C1-C6 haloalkoxy, C1-C3haloalkoxy C1-C3haloalkoxy, C1-C6haloalkylthio, C1-C6haloalkylsulfinyl and C1-C6haloalkylsulfonyl; X3 is selected from the group consisting of a hydrogen atom, halogen atom, cyano, nitro, C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy and C1-C6 alkylthio; X4 is selected from the group consisting of a hydrogen atom, halogen atom, cyano, C1-C4alkyl, C1-C4alkoxy and C1-C4haloalkoxy; R3 is —C(R3a)(R3b)R3c, where R3a and R3b independently of each other are a halogen atom, or R3a and R3b together form 3- to 6-membered ring together with the carbon atom bonding them by forming a C2-C5haloalkylene chain, and R3c is selected from the group consisting of a hydrogen atom, halogen atom, C1-C5alkyl, C1-C5haloalkyl, C1-C4haloalkoxy and C1-C4haloalkylthio, with a proviso that in case where X1 is a fluorine atom, chlorine atom or trifluoromethyl, and both X2 and X3 are a hydrogen atom, in case where both X1 and X2 are fluorine atom and X3 is a hydrogen atom, and in case where both X1 and X2 are trifluoromethyl and X3 is a hydrogen atom, R3c is a hydrogen atom, chlorine atom, bromine atom, iodine atom, C1-C5alkyl, C1-C5haloalkyl, C1-C4haloalkoxy or C1-C4haloalkylthio.
摘要翻译：其中X 1选自卤素原子，-SF 5，C 1 -C 6卤代烷基，羟基C 1 -C 6卤代烷基，C 1 -C 6烷氧基C 1 -C 6卤代烷基，C 3 -C 8卤代环烷基，C 1 -C 6卤代烷氧基，C 1 -C 3卤代烷氧基，C 1 -C 3卤代烷氧基， C 6卤代烷硫基，C 1 -C 6卤代烷基亚磺酰基和C 1 -C 6卤代烷基磺酰基; X 3选自氢原子，卤素原子，氰基，硝基，C 1 -C 6烷基，C 1 -C 6卤代烷基，C 1 -C 6烷氧基和C 1 -C 6烷硫基; X 4选自氢原子，卤素原子，氰基，C 1 -C 4烷基，C 1 -C 4烷氧基和C 1 -C 4卤代烷氧基; R3是-C（R3a）（R3b）R3c，其中R3a和R3b彼此独立地是卤素原子，或者R3a和R3b与通过形成C2- C5卤代烷基链，R3c选自氢原子，卤素原子，C1-C5烷基，C1-C5卤代烷基，C1-C4卤代烷氧基和C1-C4卤代烷硫基，条件是在X1为氟原子的情况下，氯原子或三氟甲基，X2和X3均为氢原子，X1和X2均为氟原子，X3为氢原子的情况下，X1和X2均为三氟甲基，X3为氢原子时，R3c为氢原子，氯原子，溴原子，碘原子，C1-C5烷基，C1-C5卤代烷基，C1-C4卤代烷氧基或C1-C4卤代烷硫基。

3. 发明授权

US09308193B2 Kinase inhibitors for the treatment of cancer 有权
标题翻译：用于治疗癌症的激酶抑制剂
公开(公告)号：US09308193B2
公开(公告)日：2016-04-12
申请号：US14387270
申请日：2013-03-22
申请人： PITNEY PHARMACEUTICALS PTY LIMITED
发明人： David Lawson Morris
IPC分类号： A61K31/165 , C07C233/00 , A61K31/277 , C07C255/29 , A61K31/275 , C07C317/44 , C07C323/62
CPC分类号： A61K31/277 , A61K31/275 , C07C255/29 , C07C317/44 , C07C323/62
摘要： The present invention relates to kinase inhibitors for the treatment of cancer. Specifically, the present invention relates to the use of aminoactonitrile derivatives (AADs) in the treatment of cancer.
摘要翻译：本发明涉及用于治疗癌症的激酶抑制剂。具体而言，本发明涉及氨基糖衍生物（AAD）在癌症治疗中的应用。

4. 发明申请

US20150376120A1 ALBICIDIN DERIVATIVES, THEIR USE AND SYNTHESIS 审中-公开
标题翻译：阿比西丁衍生物，其使用和合成
公开(公告)号：US20150376120A1
公开(公告)日：2015-12-31
申请号：US14768323
申请日：2014-02-14
申请人： TECHNISCHE UNIVERSITÄT BERLIN
发明人： Roderich SÜSSMUTH , Julian KRETZ , Vivien SCHUBERT , Alexander PESIC , Manuela HÜGELLAND , Monique ROYER , Stéphane COCIANCICH , Philippe ROTT , Dennis KERWAT , Stefan GRÄTZ
IPC分类号： C07C255/44 , C07D237/24 , C07D241/24 , C07D213/81 , C07F9/06 , C07D263/24 , C07D209/34 , C07D207/34 , C07D317/46 , C07D311/12 , C07D295/155 , C07D277/56
CPC分类号： C07C255/44 , C07C233/83 , C07C237/42 , C07C255/03 , C07C255/29 , C07C255/57 , C07C275/42 , C07C311/21 , C07C311/46 , C07C311/47 , C07C2601/02 , C07C2601/08 , C07C2601/14 , C07C2601/18 , C07C2603/74 , C07D207/34 , C07D209/34 , C07D213/81 , C07D237/24 , C07D241/24 , C07D241/28 , C07D263/24 , C07D277/56 , C07D295/14 , C07D295/155 , C07D307/56 , C07D311/12 , C07D317/08 , C07D317/46 , C07D333/38 , C07F9/062 , C07F9/09 , C07F9/12
摘要： Antibiotically active compounds characterized by general formula (I), wherein X1, BB, BC, BD, BE and X2 are building blocks with D1, D2, D3, D4 or D5 being linkers which include carbon, sulphur, nitrogen, phosphor and/or oxygen atoms and which are covalently connecting the moities BA and BB, BB and BC, BC and BD, BD and BE and BE and BF, respectively, and wherein in particular the building block BC comprises an amino acid derivative. The compounds for use in a method of treatment of diseases, in particular for use in a method of treatment of bacterial infections are also disclosed.
摘要翻译：其特征在于通式（I）的抗生素活性化合物，其中X1，BB，BC，BD，BE和X2是具有D1，D2，D3，D4或D5的结构单元，其包括碳，硫，氮，磷和/或氧原子，并且它们分别共价连接绝缘体BA和BB，BB和BC，BC和BD，BD和BE和BE和BF，并且其中结构单元BC包含氨基酸衍生物。还公开了用于治疗疾病的方法的化合物，特别是用于治疗细菌感染的方法中的化合物。

5. 发明申请

US20150266881A1 CYCLOPROPANAMINE COMPOUND AND USE THEREOF 有权
标题翻译：环丙基胺化合物及其用途
公开(公告)号：US20150266881A1
公开(公告)日：2015-09-24
申请号：US14435085
申请日：2013-10-11
申请人： TAKEDA PHARMACEUTICAL COMPANY LIMITED
发明人： Naoki Tomita , Daisuke Tomita , Yusuke Tominari , Shinichi Imamura , Shinji Morimoto , Takuto Kojima , Masashi Toyofuku , Yasushi Hattori , Tomohiro Kaku , Mitsuhiro Ito
IPC分类号： C07D487/04 , C07D231/38 , C07C237/38 , C07C237/30 , C07D241/12 , C07D213/36 , C07D471/04 , C07D207/46 , C07D241/18 , C07D319/18 , C07D265/36 , C07D333/20 , C07D285/135 , C07D277/38 , C07D405/12 , C07D417/12 , C07D413/12 , C07D223/12 , C07D513/04 , C07C237/40
CPC分类号： C07D487/04 , A61K45/06 , C07C237/30 , C07C237/38 , C07C237/40 , C07C255/29 , C07C255/58 , C07C255/60 , C07C317/40 , C07C2601/02 , C07C2601/04 , C07C2601/08 , C07C2601/14 , C07D207/12 , C07D207/46 , C07D211/58 , C07D213/36 , C07D213/40 , C07D223/12 , C07D231/38 , C07D231/40 , C07D241/12 , C07D241/18 , C07D261/14 , C07D265/36 , C07D277/38 , C07D285/135 , C07D295/135 , C07D309/14 , C07D319/18 , C07D333/20 , C07D405/12 , C07D413/12 , C07D417/12 , C07D471/04 , C07D513/04
摘要： The present invention provides a compound having a lysine specific demethylase 1 inhibitory action, and useful as a medicament such as a prophylactic or therapeutic agent for schizophrenia, Alzheimer's disease, Parkinson's disease or Huntington's disease, and the like. The present invention relates to a compound represented by the formula wherein A is a hydrocarbon group optionally having substituent(s), or a heterocyclic group optionally having substituent(s); B is a benzene ring optionally having further substituent(s); R1, R2 and R3 are each independently a hydrogen atom, a hydrocarbon group optionally having substituent(s), or a heterocyclic group optionally having substituent(s); A and R1 are optionally bonded to each other to form, together with the adjacent nitrogen atom, a cyclic group optionally having substituent(s); and R2 and R3 are optionally bonded to each other to form, together with the adjacent nitrogen atom, a cyclic group optionally having substituent(s), or a salt thereof.
摘要翻译：本发明提供了具有赖氨酸特异性脱甲基酶1抑制作用的化合物，可用作精神分裂症，阿尔茨海默病，帕金森病或亨廷顿病等预防或治疗药物等药物。本发明涉及由下式表示的化合物：其中A是任选具有取代基的烃基或任选具有取代基的杂环基; B是任选具有其它取代基的苯环; R 1，R 2和R 3各自独立地为氢原子，任选具有取代基的烃基或任选具有取代基的杂环基; A和R1任选地彼此键合，与相邻的氮原子一起形成任选具有取代基的环状基团; R 2和R 3可以相互键合，与相邻的氮原子一起形成任选具有取代基的环状基团或其盐。

6. 发明授权

US08901302B2 Pyrazino[2,3-D]isoxazole derivative which is useful as a production intermediate of pyrazine carboxamide derivative 有权
标题翻译：吡嗪并[2,3-D]异恶唑衍生物，其可用作吡嗪甲酰胺衍生物的生产中间体
公开(公告)号：US08901302B2
公开(公告)日：2014-12-02
申请号：US13886483
申请日：2013-05-03
申请人： FUJIFILM Corporation , Toyama Chemical Co., Ltd.
发明人： Kouki Nakamura , Takeshi Murakami , Hiroyuki Naitou , Naoyuki Hanaki , Katsuyuki Watanabe
IPC分类号： C07D241/50 , C07C239/18 , C07D498/04 , C07C251/38 , C07C255/23 , C07C237/06 , C07D261/18 , C07C255/29 , C07D241/18 , C07D241/24
CPC分类号： C07D241/24 , C07C237/06 , C07C239/18 , C07C251/38 , C07C255/23 , C07C255/29 , C07D241/18 , C07D261/18 , C07D498/04
摘要： The object of the present invention is to provide a compound which is useful as a production intermediate of pyrazine carboxamide derivative such as 6-fluoro-3-hydroxy-2-pyrazine carboxamide. The present invention provides a pyrazino[2,3-d]isoxazole derivative represented by the formula (I): wherein X represents a halogen atom, a hydroxyl group or a sulfamoyloxy group, and Y represents —C(═O)R or —CN; wherein R represents a hydrogen atom, an alkoxy group an aryloxy group, an alkyl group, an aryl group or an amino group.
摘要翻译：本发明的目的是提供一种可用作吡嗪甲酰胺衍生物如6-氟-3-羟基-2-吡嗪甲酰胺的制备中间体的化合物。本发明提供由式（I）表示的吡嗪并[2,3-d]异恶唑衍生物：其中X表示卤素原子，羟基或氨磺酰氧基，Y表示-C（= O）R或 - CN; 其中R表示氢原子，烷氧基，芳氧基，烷基，芳基或氨基。

7. 发明授权

US08637576B2 Benzamide derivatives and uses related thereto 失效
标题翻译：苯甲酰胺衍生物及其用途
公开(公告)号：US08637576B2
公开(公告)日：2014-01-28
申请号：US12582535
申请日：2009-10-20
申请人： Jay P. Powers , Michael R. Degraffenreid , Xiao He , Lisa D. Julian , Dustin L. McMinn , Daqing Sun , Yosup Rew , Xuelei Yan
发明人： Jay P. Powers , Michael R. Degraffenreid , Xiao He , Lisa D. Julian , Dustin L. McMinn , Daqing Sun , Yosup Rew , Xuelei Yan
IPC分类号： A61K31/165 , A61K31/44
CPC分类号： C07D277/28 , C07C235/42 , C07C235/54 , C07C237/42 , C07C255/29 , C07C255/31 , C07C255/44 , C07C255/46 , C07C255/60 , C07C317/36 , C07C2601/02 , C07C2601/04 , C07C2601/08 , C07C2601/14 , C07C2602/42 , C07D211/16 , C07D211/18 , C07D211/22 , C07D211/34 , C07D211/38 , C07D211/52 , C07D211/60 , C07D211/64 , C07D213/40 , C07D213/61 , C07D213/74 , C07D213/81 , C07D213/84 , C07D213/89 , C07D233/64 , C07D295/192 , C07D307/22 , C07D309/14 , C07D333/20
摘要： Benzamide derivatives of formulae I and II, and pharmaceutically acceptable salts, solvates, stereoisomers, and prodrugs thereof, and pharmaceutical compositions comprising the same, are described and have therapeutic utility, particularly in the treatment of diabetes, obesity, and related conditions and disorders: wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, and R12 are defined as provided herein.
摘要翻译：描述了式I和II的苯甲酰胺衍生物及其药学上可接受的盐，溶剂化物，立体异构体和前药，以及包含其的药物组合物，并具有治疗用途，特别是治疗糖尿病，肥胖症和相关病症和病症：其中R 1，R 2，R 3，R 4，R 5，R 6，R 7，R 8，R 9，R 10，R 11和R 12如本文所提供。

8. 发明申请

US20130261324A1 SYNTHESIS OF ALISKIREN 有权
标题翻译： ALISKIREN的合成
公开(公告)号：US20130261324A1
公开(公告)日：2013-10-03
申请号：US13879849
申请日：2011-10-19
申请人： Rama Shankar , Vadali Lakshmana Rao , Palla Vijay Kumar , Saidugari Swamy , Dasari Srinivasa Rao , Srinivasa Rao Potla , Mittapelly Nagaraju , Jaldu Ravikanth , Vijaya Krishna Ravi , Seshadri Rao Manukonda , Dandala Ramesh
发明人： Rama Shankar , Vadali Lakshmana Rao , Palla Vijay Kumar , Saidugari Swamy , Dasari Srinivasa Rao , Srinivasa Rao Potla , Mittapelly Nagaraju , Jaldu Ravikanth , Vijaya Krishna Ravi , Seshadri Rao Manukonda , Dandala Ramesh
IPC分类号： C07C231/14 , C07C43/215 , C07C247/10
CPC分类号： C07C231/14 , C07C43/215 , C07C231/12 , C07C241/00 , C07C247/10 , C07C255/29 , C07D307/33 , C07C237/22
摘要： The present invention provides novel process for the preparation of renin inhibitor Aliskiren or its derivatives, and its pharmaceutically acceptable salts. The present invention also provides novel intermediates used in the preparation of Aliskiren.
摘要翻译：本发明提供了制备肾素抑制剂阿利吉仑或其衍生物及其药学上可接受的盐的新方法。本发明还提供了用于制备阿利吉仑的新型中间体。

9. 发明授权

US08318748B2 Cathepsin cysteine protease inhibitors 有权
标题翻译：组织蛋白酶半胱氨酸蛋白酶抑制剂
公开(公告)号：US08318748B2
公开(公告)日：2012-11-27
申请号：US13115462
申请日：2011-05-25
申请人： Christopher I. Bayly , Cameron Black , Serge Leger , Chun Sing Li , Dan McKay , Christophe Mellon , Jacques Yves Gauthier , Vouy-Linh Truong , Cheuk Lau , Michel Therien , Michael J. Green , Bernard L. Hirschbein , James William Janc , James T. Palmer , Chitra Baskaran
发明人： Christopher I. Bayly , Cameron Black , Serge Leger , Chun Sing Li , Dan McKay , Christophe Mellon , Jacques Yves Gauthier , Vouy-Linh Truong , Cheuk Lau , Michel Therien , Michael J. Green , Bernard L. Hirschbein , James William Janc , James T. Palmer , Chitra Baskaran
IPC分类号： A61K31/4965 , A61K31/66 , A61K31/44 , A61K31/445 , A61K31/425 , A61K31/415
CPC分类号： C07C237/20 , A61K31/165 , A61K31/18 , A61K31/4174 , A61K31/426 , A61K31/44 , A61K31/4418 , A61K31/495 , C07C255/25 , C07C255/29 , C07C255/46 , C07C255/58 , C07C259/10 , C07C311/37 , C07C317/32 , C07C2601/02 , C07C2601/14 , C07D209/08 , C07D213/38 , C07D213/57 , C07D213/64 , C07D213/70 , C07D213/89 , C07D215/12 , C07D231/12 , C07D233/64 , C07D239/26 , C07D241/12 , C07D261/08 , C07D263/32 , C07D271/06 , C07D277/28 , C07D277/30 , C07D295/135 , C07D295/155 , C07D307/52 , C07D333/20 , C07D401/04 , C07D417/04
摘要： This invention relates to a novel class of compounds which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsins K, L, S and B. These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis.
摘要翻译：本发明涉及一类新的化合物，它们是半胱氨酸蛋白酶抑制剂，包括但不限于组织蛋白酶K，L，S和B的抑制剂。这些化合物可用于治疗其中指示抑制骨吸收的疾病，例如骨质疏松症

10. 发明申请

US20120283216A1 FUNGICIDAL 2-(BICYCLIC ARYLOXY)CARBOXAMIDES 审中-公开
标题翻译：杀真菌2-（双环芳烃）碳氧化物
公开(公告)号：US20120283216A1
公开(公告)日：2012-11-08
申请号：US13513056
申请日：2010-12-22
申请人： Alvin Donald Crews, JR. , Amy X. Ding , Chi-Ping Tseng
发明人： Alvin Donald Crews, JR. , Amy X. Ding , Chi-Ping Tseng
IPC分类号： A01N37/18 , A01N37/34 , C07C235/06 , C07C243/28 , A01N37/28 , C07F9/32 , A01N57/22 , C07C271/20 , A01N47/12 , C07C327/30 , C07F7/10 , A01N55/10 , C07D215/20 , A01N43/42 , C07D217/24 , A01P3/00 , C07C255/29
CPC分类号： C07D217/24 , A01N39/04 , A01N43/42 , A01N55/00 , C07C235/08 , C07C255/29 , C07C271/20 , C07C323/21 , C07C327/30 , C07C327/42 , C07C2601/02 , C07C2601/14 , C07D215/20 , C07F9/3211 , C07F9/60 , C07F9/62
摘要： Disclosed are compounds of Formula 1, N-oxides, and salts thereof, wherein Q is O or S; Z1 and Z2 are each independently CR9 or N; and R1, R2, R3, R4, R5, R6, R7, R8 and R9 are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling plant disease caused by a fungal pathogen comprising applying an effective amount of a compound or a composition of the invention.
摘要翻译：公开了式1的化合物，N-氧化物及其盐，其中Q是O或S; Z1和Z2各自独立地为CR9或N; 并且R 1，R 2，R 3，R 4，R 5，R 6，R 7，R 8和R 9如本公开所定义。还公开了含有式1化合物的组合物和用于控制由真菌病原体引起的植物病害的方法，包括施用有效量的本发明化合物或组合物。

你已经成功收藏专利！

检索式保存成功!

IPRDB

热门服务

关于我们

友情链接

联系方式