法尼甾体X受体
化学
兴奋剂
喹啉
双环分子
萘
立体化学
药理学
化学合成
受体
核受体
体外
生物化学
有机化学
基因
转录因子
医学
作者
Jonathan Y. Bass,Justin A. Caravella,Lihong Chen,Katrina L. Creech,David N. Deaton,Kevin P. Madauss,Harry B. Marr,Robert B. McFadyen,Aaron B. Miller,Wendy Y. Mills,Frank Navas,Derek J. Parks,Terrence L. Smalley,Paul K. Spearing,Dan Todd,Shawn P. Williams,G. Bruce Wisely
标识
DOI:10.1016/j.bmcl.2010.12.089
摘要
To improve on the drug properties of GSK8062 1b, a series of heteroaryl bicyclic naphthalene replacements were prepared. The quinoline 1c was an equipotent FXR agonist with improved drug developability parameters relative to 1b. In addition, analog 1c lowered body weight gain and serum glucose in a DIO mouse model of diabetes.
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