发明名称 Benzylidene-1,3-dihydro-indol-2-one derivatives as receptor tyrosine kinase inhibitors, particularly of raf kinases
摘要 Compounds of general formula (I) wherein: R1 is H or optionally joined with R2 to form a fused ring selected from the group consisting of five to ten membered aryl, heteroaryl or heterocyclyl rings, R2 and R3 are independently H, HET, aryl, C1-12 aliphatic, CN, NO2, halogen, R10, -OR10, -SR10, -S(O)R10, -SO2R10, -NR10R11, -NR11R12, -NR12COR11, -NR12CO2R11, -NR12CONR11R12, -NO12SO2R11, -NR12C(NR 12)NHR11, -COR11, -CO2R11, -CONR12R11, -SO2NR12R11, -OCONR12R11, C(NR12)NR12R11, R6 and R7 are independently halogen, CN, NO2, -CONR10R11, -SO2NR10R11, -NR10R11, or -OR11, where R10 and R11 are as defined below; R8 is OH, NHSO2R12 or NHCOCF3; and their use in therapy, especially in the treatment of disorders mediated by cRaf1 kinase.
申请公布号 AU9158498(A) 申请公布日期 1999.03.16
申请号 AU19980091584 申请日期 1998.08.04
申请人 GLAXO GROUP LIMITED 发明人 ROBERT WALTON MCNUTT;DAVID KENDALL JUNG;PHILIP ANTHONY HARRIS;ROBERT NEIL HUNTER III;JAMES MARVIN VEAL;SCOTT DICKERSON;KAREN ELIZABETH LACKEY;MICHAEL ROBERT PEEL
分类号 C07D487/04;A61K31/404;A61K31/407;A61K31/41;A61K31/422;A61K31/4245;A61K31/427;A61K31/429;A61K31/437;A61K31/4439;A61K31/496;A61K31/53;A61K31/5377;A61P1/16;A61P3/10;A61P7/02;A61P9/00;A61P9/10;A61P13/12;A61P17/02;A61P17/06;A61P19/02;A61P25/00;A61P29/00;A61P35/00;A61P37/06;A61P43/00;C07D209/34;C07D401/04;C07D401/06;C07D401/12;C07D403/04;C07D405/06;C07D409/04;C07D409/06;C07D413/04;C07D413/06;C07D417/04;C07D417/06;C07D417/10;C07D417/12;C07D471/04;C07D513/04;C07D521/00 主分类号 C07D487/04
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