发明名称 Inhibitors of cytochrome P450
摘要 The present application provides for a compound of Formula I,; or a pharmaceutically acceptable salt, solvate, and/or ester thereof, compositions containing such compounds, therapeutic methods that include the administration of such compounds, and therapeutic methods and include the administration of such compounds with at least one additional therapeutic agent.
申请公布号 US8759379(B2) 申请公布日期 2014.06.24
申请号 US200812340419 申请日期 2008.12.19
申请人 Gilead Sciences, Inc. 发明人 Desai Manoj C.;Hui Hon C.;Liu Hongtao;Xu Lianhong
分类号 A61K31/341;A61K31/34;A61K31/5377;A61K31/427;C07D417/12;C07D417/14;C07D493/04;C07D307/20 主分类号 A61K31/341
代理机构 代理人 Silver Joel B.
主权项 1. A compound of Formula I, or a pharmaceutically acceptable salt, wherein, X1 is selected from the group consisting of —C(O)—O—, —S(O)—, and —S(O2)—; X2 is selected from the group consisting of —O—, —NR6—C(O)—NR6—, —OC(O)NR6—, —NR6—, and —NR6C(O)O—; L is selected from the group consisting of a covalent bond, alkylene, and —CHR7—; R1 is selected from the group consisting of aryl, heteroaryl, arylalkyl, and heteroarylalkyl; each R2 is independently selected from the group consisting of H, alkyl, arylalkyl, heterocyclylalkyl, and cycloalkylalkyl wherein at least one R2 is arylalkyl; R3 is selected from the group consisting of heterocyclyl, aryl, heteroaryl, arylalkyl, and heteroarylalkyl; R4 and R5 are each independently selected from the group consisting of H, alkyl, cycloalkyl, heterocyclyl, cycloalkylalkyl, arylalkyl, and heterocyclylalkyl; each R6 is independently selected from the group consisting of H, alkyl, and cycloalkyl; and R7 is selected from the group consisting of H, alkyl, substituted alkyl, and heterocyclylalkyl; wherein each aryl, heteroaryl, cycloalkyl, heterocyclyl, cycloalkylalkyl, heterocyclylalkyl, arylalkyl, and heteroarylalkyl of R1, R2, R3, R4, R5, R6 and R7 is unsubstituted or substituted.
地址 Foster City CA US