[EN] AMINO QUINOLINE DERIVATIVES INHIBITORS OF HCV<br/>[FR] DÉRIVÉS D'AMINO-QUINOLÉINE INHIBITEURS DE VHC
申请人:GILEAD SCIENCES INC
公开号:WO2013090929A1
公开(公告)日:2013-06-20
A compound of Formula I: or a pharmaceutically acceptable salt thereof, wherein the substituents are defined herein, and methods of treating HCV infection in a patient are disclosed.
一种化合物的化学式I:或其药用可接受的盐,其中取代基在此定义,并公开了治疗患者HCV感染的方法。
Structure-based design of TACE selective inhibitors: Manipulations in the S1′–S3′ pocket
A series of beta-sulfonyl hydroxamate TACE inhibitors, bearing a butynylamino or a butynyloxy Pl' group, was designed and synthesized. Of the compounds investigated, 22 has excellent potency against isolated TACE enzyme, shows good selectivity over MMP-2 and MMP- 13, and oral activity in an in vivo mouse model of TNF-alpha( production. (c) 2007 Elsevier Ltd. All rights reserved.