受体
兴奋剂
滥交
药理学
药品
化学
配体(生物化学)
5-HT5A受体
功能选择性
药物作用
G蛋白偶联受体
生物物理学
计算生物学
立体化学
生物
生物化学
生态学
标识
DOI:10.1016/s0165-6147(00)89020-3
摘要
The description of drug effects on receptor proteins is based on models and equations used to describe mass-action kinetics of molecules and inert surfaces. These models provide an adequate description of drug affinity, that is, how well a molecule binds to a receptor protein, but the way in which ligands change receptor populations to impart signals to cells remains to be determined. In the first of two articles, Terry Kenakin discusses a basic question in receptor pharmacology, namely the nature of ligand efficacy.
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