发明授权
US08546394B2 Substituted [1,2,4]triazolo[4,3-A]pyrazine 11-beta-hydroxysteroid dehydrogenase inhibitors
有权
取代的[1,2,4]三唑并[4,3-A]吡嗪11-β-羟基类固醇脱氢酶抑制剂
- 专利标题: Substituted [1,2,4]triazolo[4,3-A]pyrazine 11-beta-hydroxysteroid dehydrogenase inhibitors
- 专利标题(中): 取代的[1,2,4]三唑并[4,3-A]吡嗪11-β-羟基类固醇脱氢酶抑制剂
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申请号: US12595524申请日: 2008-04-16
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公开(公告)号: US08546394B2公开(公告)日: 2013-10-01
- 发明人: Jun Li , James J. Li , Stephen P. O'Connor , Haixia Wang , Lawrence J. Kennedy , Jeffrey A. Robl , Lawrence G. Hamann
- 申请人: Jun Li , James J. Li , Stephen P. O'Connor , Haixia Wang , Lawrence J. Kennedy , Jeffrey A. Robl , Lawrence G. Hamann
- 申请人地址: US NJ Princeton
- 专利权人: Bristol-Myers Squibb Company
- 当前专利权人: Bristol-Myers Squibb Company
- 当前专利权人地址: US NJ Princeton
- 代理商 Terence J. Bogie
- 国际申请: PCT/US2008/060395 WO 20080416
- 国际公布: WO2008/130951 WO 20081030
- 主分类号: A61K31/495
- IPC分类号: A61K31/495
摘要:
Novel compounds are provided which are 1 1-beta-hydroxysteroid dehydrogenase type I inhibitors. 1 1-beta-hydroxysteroid dehydrogenase type I inhibitors are useful in treating, preventing, or slowing the progression of diseases requiring 1 1-beta-hydroxysteroid dehydrogenase type I inhibitor therapy. These novel compounds have the structure: W-L-Z or stereoisomers or prodrugs or pharmaceutically acceptable salts thereof, wherein W, L are defined herein and Z is selected from the following bicyclic heteroaryl groups: (a), (b), (c), (d).
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