地址1
盘状结构域
受体
计算生物学
医学
化学
生物信息学
药理学
计算机科学
生物
内科学
受体酪氨酸激酶
作者
Daniel E. Jeffries,Corina M. Borza,Anna L. Blobaum,Ambra Pozzi,Craig W. Lindsley
标识
DOI:10.1021/acsmedchemlett.9b00382
摘要
[Image: see text] Herein, we report the discovery of a potent and selective dual DDR1/2 inhibitor, 7e (VU6015929), displaying low cytotoxicity, good kinome selectivity, and possessing an acceptable in vitro DMPK profile with good rodent in vivo pharmacokinetics. VU6015929 potently blocks collagen-induced DDR1 activation and collagen-IV production, suggesting DDR1 inhibition as an exciting target for antifibrotic therapy.
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