化学
选择性
CYP3A4型
肾素-血管紧张素系统
联苯
生物利用度
效力
乙醚
肾素抑制剂
药理学
立体化学
戒指(化学)
体内
体外
生物化学
酶
内分泌学
有机化学
医学
细胞色素P450
血压
催化作用
生物技术
生物
作者
Jing Yuan,R. David Simpson,Wei Zhao,Colin M. Tice,Zhenrong Xu,Salvacion Cacatian,Lanqi Jia,Patrick T. Flaherty,Joan Guo,Alexey Ishchenko,Zhongren Wu,Brian M. McKeever,Boyd B. Scott,Yuri Bukhtiyarov,Jennifer Berbaum,Reshma Panemangalore,Ross Bentley,Christopher Doe,Richard K. Harrison,Gerard M. McGeehan
标识
DOI:10.1016/j.bmcl.2011.06.043
摘要
Structure-based design led to the discovery of a novel class of renin inhibitors in which an unprecedented phenyl ring filling the S1 site is attached to the phenyl ring filling the S3 pocket. Optimization for several parameters including potency in the presence of human plasma, selectivity against CYP3A4 inhibition and improved rat oral bioavailability led to the identification of 8d which demonstrated antihypertensive efficacy in a transgenic rat model of human hypertension.
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