组织蛋白酶
半胱氨酸蛋白酶
氰胺
体内
组织蛋白酶O
化学
组织蛋白酶A
药物发现
组织蛋白酶
组织蛋白酶L
组织蛋白酶E
生物化学
半胱氨酸
药理学
酶
生物
生物技术
作者
Dramane I. Lainé,Michael Palovich,Brent W. McCleland,Emilie Petit-Jean,Isabelle Delhom,Haibo Xie,Jianghe Deng,Guoliang Lin,Roderick Davis,Anaïs Jolit,Neysa Nevins,Baoguang Zhao,Jim Villa,Jessica L. Schneck,Patrick McDevitt,Robert Midgett,Casey Kmett,Sandra Umbrecht,Brian Peck,Alicia B. Davis,David Bettoun
摘要
The discovery of potent and selective cyanamide-based inhibitors of the cysteine protease cathepsin C is detailed. Optimization of the template with regard to plasma stability led to the identification of compound 17, a potent cathepsin C inhibitor with excellent selectivity over other cathepsins and potent in vivo activity in a cigarette smoke mouse model.
科研通智能强力驱动
Strongly Powered by AbleSci AI