Synthesis and pharmacological characterization of C4-disubstituted analogs of 1S,2S,5R,6S-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylate: identification of a potent, selective metabotropic glutamate receptor agonist and determination of agonist-bound human mGlu2 and mGlu3 amino terminal domain structures.
第一作者:
James A,Monn
第一单位:
Discovery Chemistry Research and Technologies, ‡Quantitative Biology, §Structural Biology, ∥Drug Disposition, and ⊥Neuroscience Research, Eli Lilly and Company , Indianapolis, Indiana 46285, United States.
作者:
医学主题词
动物(Animals);结晶学, X线(Crystallography, X-Ray);人类(Humans);男(雄)性(Male);模型, 分子(Models, Molecular);蛋白质结构, 三级(Protein Structure, Tertiary);大鼠(Rats);大鼠, Sprague-Dawley(Rats, Sprague-Dawley);受体, 亲代谢性谷氨酸盐(Receptors, Metabotropic Glutamate);螺环化合物(Spiro Compounds)
DOI
10.1021/jm501612y
PMID
25602126
发布时间
2016-11-25
- 浏览101
Journal of medicinal chemistry
1776-94页
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