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 chlorides and ADAM-10 modulators therefrom.
申请公布号 US7498358(B2) 申请公布日期 2009.03.03
申请号 US20050498338 申请日期 2005.05.11
申请人 EXELIXIS, INC. 发明人 BROWN S. DAVID;CANNE-BANNEN LYNNE;CO ERICK WANG;JAMMALAMADAKA VASU;KHOURY RICKARD GEORGE;KIM MOON HWAN;LE DONNA T.;TSUHAKO AMY LEW;MAC MORRISON B.;MAMO SHUMEYE;NUSS JOHN M.;PRISBYLLA MICHAEL P.;XU WEI
分类号 A61K31/40;C07C311/19;A61K31/16;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;C07C259/06;C07C259/08;C07C303/02;C07C303/40;C07C309/87;C07C311/29;C07D207/09;C07D211/34;C07D213/32;C07D213/56;C07D213/65;C07D213/68;C07D213/70;C07D233/48;C07D233/54;C07D295/13;C07D295/15;C07D295/185;C07D295/215;C07D311/70;C07D409/04 主分类号 A61K31/40
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