化学
酪氨酸激酶
体外
药理学
口服活性
生物利用度
激酶
烷氧基
立体化学
原癌基因酪氨酸蛋白激酶Src
受体
生物化学
有机化学
医学
烷基
作者
Richard Ducray,Peter Ballard,Bernard Barlaam,Mark Hickinson,Jason G. Kettle,Donald Ogilvie,Catherine B. Trigwell
标识
DOI:10.1016/j.bmcl.2007.12.035
摘要
Novel 4-anilino-1H-pyrazolo[3,4-d]pyrimidines have been synthesized and evaluated in vitro for erbB2 and EGFR kinase inhibition. A representative compound displaying oral bioavailability in rat and dog illustrates the potential of this series to provide orally active erbB2 inhibitors.
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