亲缘关系
配体(生物化学)
选择性
结合位点
化学
卡帕
立体化学
受体
κ-阿片受体
结合亲和力
类阿片
结合选择性
生物化学
数学
几何学
催化作用
出处
期刊:Molecular Pharmacology
[American Society for Pharmacology and Experimental Therapeutics]
日期:1989-08-01
卷期号:36 (2): 265-272
被引量:446
标识
DOI:10.1016/s0026-895x(25)09190-4
摘要
Methods are described for studying mu, delta, and kappa opioid binding sites, each without interference from the others. A large array of ligands has been characterized by ligand selectivity profiles, graphic depictions of affinities and selectivities. Binding site signatures have been derived, which uniquely describe each of the three types of sites. The mu, delta, and kappa binding sites have interesting common features and distinctive differences.
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