发明名称 INHIBITING RAF KINASE USING SUBSTITUTED HETEROCYCLIC UREA
摘要 <p><P>PROBLEM TO BE SOLVED: To provide an isooxazolyl urea compound having an activity of inhibiting RAF kinase, useful in treating solid cancer, for example a cancerous tumor [such as a cancerous tumor of a lung, spleen, thyroid, bladder, or colon, or a disease of bone marrow (bone marrow leukemia for example)], or an adenoma (a villus-like colon adenoma, for example), or the like. <P>SOLUTION: The compound is represented by the following formula (in the formula, R1 is selected from the group consisting of 3-10C alkyl, 3-10C cycloalkyl, 3-10C halosubstituted alkyl up to perhaloalkyl and 3-10C halosubstituted cycloalkyl up to perhalocycloalkyl, and B represents phenyl, phenyl substituted with pyridyl or -Y-Ar, pyridinyl, indolinyl, isoquinolinyl, quinolinyl or naphthyl). <P>COPYRIGHT: (C)2010,JPO&INPIT</p>
申请公布号 JP2010065041(A) 申请公布日期 2010.03.25
申请号 JP20090237895 申请日期 2009.10.15
申请人 BAYER CORP 发明人 DUMAS JACQUES;KHIRE UDAY;LOWINGER TIMOTHY BRUNO;PAULSEN HOLGER;RIEDL BERND;SCOTT WILLIAM J;SMITH ROGER A;WOOD JILL E;HATOUM-MOKDAD HOLIA;JOHNSON JEFFREY;LEE WENDY;REDMAN ANIKO
分类号 A61K31/17;C07D261/14;A61K31/34;A61K31/381;A61K31/41;A61K31/415;A61K31/42;A61K31/422;A61K31/4245;A61K31/425;A61K31/427;A61K31/428;A61K31/433;A61K31/4427;A61K31/4433;A61K31/4436;A61K31/4439;A61K31/444;A61K31/454;A61K31/4709;A61K31/496;A61K31/497;A61K31/506;A61K31/5377;A61P35/00;A61P35/02;A61P43/00;C07C275/26;C07C275/28;C07D231/38;C07D231/40;C07D257/06;C07D271/10;C07D271/113;C07D277/28;C07D285/12;C07D285/135;C07D333/36;C07D401/12;C07D405/14;C07D409/12;C07D413/12;C07D413/14;C07D417/12;C07D417/14;C07D521/00 主分类号 A61K31/17
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