化学
岩石2
选择性
氨基甲酸酯
内酰胺
酰胺
生物甾体
立体化学
苯胺
环肽
化学合成
酶抑制剂
甲酰胺
尿素
结构-活动关系
组合化学
基因亚型
激酶
生物化学
酶
肽
有机化学
体外
Rho相关蛋白激酶
基因
催化作用
作者
Zilun Hu,Doree Sitkoff,Peter W. Glunz,Zou Yan,Cailan Wang,J.K. Muckelbauer,Leonard P. Adam,Ruth R. Wexler,Mimi L. Quan
标识
DOI:10.1016/j.bmcl.2023.129304
摘要
Derivatives of lactam, cyclic urea and carbamate were explored as aniline amide replacements in a series of phthalazinone-based ROCK inhibitors. Potent ROCK2 inhibitors such as 22 were identified with excellent overall kinase selectivity as well as good isoform selectivity over ROCK1.
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