发明名称 N-benzylamide substituted derivatives of 2-(acylamido)acetic acid and 2-(acylamido)propionic acids: potent neurological agents
摘要 A first aspect of the invention is a compound (sometimes also referred to herein as an “active agent” or “active compound”) of Formula I or Ia:; or a pharmaceutically acceptable salt or prodrug thereof. Compositions thereof and methods of using the same (e.g. for the treatment of a neurological disease) are also described.
申请公布号 US8933065(B2) 申请公布日期 2015.01.13
申请号 US201012884963 申请日期 2010.09.17
申请人 The University of North Carolina at Chapel Hill 发明人 Kohn Harold L.;Salomé Christophe;Park Ki Duk;Salomé-Grosjean Elise
分类号 A61K31/396;A61K31/16;C07D521/00;C07C233/88;C07C229/02;C07D213/40;C07D213/56;C07C235/08;C07C233/18;C07D229/00;C07D277/30;C07D307/68 主分类号 A61K31/396
代理机构 Myers Bigel Sibley & Sajovec, P.A. 代理人 Myers Bigel Sibley & Sajovec, P.A.
主权项 1. A compound of Formula I:wherein: R1 is alkyl or cycloalkyl, each of which can be unsubstituted or substituted with from one to four independently selected electron-donating or electron-withdrawing groups; R2, Rv and Rw are each independently hydrogen, alkyl, cycloalkyl, heterocyclo, aryl, or heteroaryl, which alkyl, cycloalkyl, heteroacylclo, aryl, or heteroaryl can be unsubstituted or substituted with from one to four independently selected electron-donating or electron-withdrawing groups, or R2, Rv and Rw are each independently an electron-donating or electron-withdrawing group; R3a, R3b and R4 are each independently hydrogen, an electron donating or electron-withdrawing group, or alkyl, cycloalkyl, alkenyl, alkynyl, aryl, heterocyclo, heteroaryl, arylalkyl, heteroarylalkyl, or heterocycloalkyl, each of which can be unsubstituted or substituted with from one to four independently selected electron-donating or electron-withdrawing groups; R5 and R6 are each independently H or alkyl; and X′ is S or O; or a pharmaceutically acceptable salt or prodrug thereof.
地址 Chapel Hill NC US