受体
药理学
μ-阿片受体
敌手
效力
部分激动剂
作者
Guo-Hua Chu,Minghua Gu,Joel A. Cassel,Serge Belanger,Thomas M. Graczyk,Robert N. DeHaven,Nathalie Conway-James,Michael Koblish,Patrick J. Little,Diane L. DeHaven-Hudkins,Roland E. Dolle
标识
DOI:10.1016/j.bmcl.2007.01.053
摘要
A novel series of malonamide derivatives was synthesized. These amides were shown to be potent and selective kappa opioid receptor agonists.
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