发明名称 HUMAN ADAM-10 INHIBITORS
摘要 The present invention provides compounds useful for inhibiting the ADAM-10 protein. Such compounds are useful in the in vitro study of the role of ADAM - 10 (and its inhibition) in biological processes. The present invention also comprises pharmaceutical compositions comprising one or more ADAM-10 inhibitors according to the invention in combination with a pharmaceutically acceptable carrier. Such compositions are useful for the treatment of cancer , arthritis, and diseases related to angiogenesis. Correspondingly, the invention also comprises methods of treating forms of cancer, arthritis, and diseases related to angiogenesis in which ADAM-10 plays a critical role. The invention also provides methods for making bis-aryl ether sulfonyl chorides and ADAM-10 modulators therefrom.
申请公布号 CA2473938(A1) 申请公布日期 2003.06.26
申请号 CA20022473938 申请日期 2002.12.13
申请人 EXELIXIS INC. 发明人 PRISBYLLA, MICHAEL P.;MAMO, SHUMEYE;NUSS, JOHN M.;XU, WEI;CANNE, LYNNE;CO, ERICK W.;MAC, MORRISON B.;LEW, AMY;KIM, MOON HWAN;BROWN, S. DAVID;LE, DONNA T.;JAMMALAMADAKA, VASU;KHOURY, RICHARD G.
分类号 A61K31/40;A61K31/18;A61K31/277;A61K31/405;A61K31/44;A61K31/4406;A61K31/4418;A61K31/445;A61K31/4462;A61K31/4465;A61K31/4965;A61K31/506;A61K31/5375;A61K31/5377;A61K31/54;A61P1/04;A61P3/10;A61P9/00;A61P9/04;A61P9/10;A61P13/12;A61P15/00;A61P17/00;A61P19/02;A61P29/00;A61P35/00;A61P43/00;C07C303/02;C07C303/40;C07C309/87;C07C311/29;C07D207/09;C07D211/34;C07D213/56;C07D213/65;C07D213/70;C07D233/48;C07D233/54;C07D295/13;C07D295/15;C07D295/185;C07D295/215;C07D311/70;C07D409/04;(IPC1-7):C07C311/19;C07C259/06;C07C259/08;A61K31/16;C07D213/32;C07D213/68 主分类号 A61K31/40
代理机构 代理人
主权项
地址