化学
选择性
喹啉
激酶
酶抑制剂
立体化学
酶
结构-活动关系
生物化学
体外
有机化学
催化作用
作者
David A. Scott,Kirsten Bell,Cheryl T. Campbell,Donald J. Cook,Les A. Dakin,David J. Del Valle,Lisa Drew,Thomas W. Gero,Maureen M. Hattersley,Charles A. Omer,Boris Tyurin,Xiaolan Zheng
标识
DOI:10.1016/j.bmcl.2008.12.044
摘要
The optimization of compounds from the 3-amido-4-anilinoquinolines series of CSF-1R kinase inhibitors is described. The series has excellent activity and kinase selectivity. Excellent physical properties and rodent PK profiles were achieved through the introduction of cyclic amines at the quinoline 6-position. Compounds with good activity in a mouse PD model measuring inhibition of pCSF-1R were identified.
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