Aryl-amino substituted pyrrolopyrimidine multi-kinase inhibiting compounds

Compounds represented by Formula (I): or stereoisomers or pharmaceutically acceptable salts thereof, are inhibitors of least two of the Abl, Aurora-A, Blk, c-Raf, cSRC, Src, PRK2, FGFR3, Flt3, Lck, Mekl, PDK-1, GSK3ss, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, IGF-lR, Ron, Ret, and KDR kinases in anima...

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Hauptverfasser: AHMED SALEH,BARBA OSCAR,BLOXHAM JASON,DAWSON GRAHAM,GATTRELL WILIAM,KITCHIN JOHN,PEGG NEIL ANTHONY,SABA IMAAD,SADIQ SHAZIA,SAMBROOK SMITH COLIN PETER,SMYTH DON,STEING AMO G.,WILKES ROBIN,PANICKER BIJO, G HANQING,MA LIFU,FOREMAN KENNETH,WENG QINGHUA,STOLZ KATHRYN
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Sprache:eng
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Zusammenfassung:Compounds represented by Formula (I): or stereoisomers or pharmaceutically acceptable salts thereof, are inhibitors of least two of the Abl, Aurora-A, Blk, c-Raf, cSRC, Src, PRK2, FGFR3, Flt3, Lck, Mekl, PDK-1, GSK3ss, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, IGF-lR, Ron, Ret, and KDR kinases in animals, including humans, for the treatment and/or prevention of various diseases and conditions such as cancer.