发明名称 Pyrazinone derivatives
摘要 The present invention relates to a compound of the general formula (I): [Ar<SUB>1 </SUB>is aryl fused to the adjacent pyrazinone ring at the 5th and 6th positions, etc., X is CO, etc., Y is CH, etc., Z is CH, etc., V is CH, etc., W<SUB>n </SUB>is -(CH<SUB>2</SUB>)<SUB>n</SUB>- (n is zero to four), R<SUB>1 </SUB>is H or optionally substituted lower alkyl, etc., R<SUB>2 </SUB>is H, etc., R<SUB>3 </SUB>and R<SUB>4 </SUB>are the same or different and are each H, etc., R<SUB>5 </SUB>and R<SUB>6 </SUB>are the same or different and are each H, hydroxy, etc.] or a pharmaceutically acceptable salt or ester thereof; a pharmaceutical composition, an inhibitor of Cdk4 and/or Cdk6 or an anti-cancer agent, containing the same as an active ingredient; and a process for preparing them.
申请公布号 US6914062(B2) 申请公布日期 2005.07.05
申请号 US20030312500 申请日期 2003.01.31
申请人 BANYU PHARMACEUTICAL CO., LTD. 发明人 HAYAMA TAKASHI;KAWANISHI NOBUHIKO;TAKAKI TOORU
分类号 A61P35/00;A61P43/00;C07D213/75;C07D277/48;C07D401/12;C07D405/12;C07D409/12;C07D417/12;C07D487/04;(IPC1-7):A01N43/58;A01N43/60;A61K31/495;A61K31/50;C07D475/00 主分类号 A61P35/00
代理机构 代理人
主权项
地址