G蛋白偶联受体
受体-配体动力学
背景(考古学)
药物发现
动力学
药品
化学
计算生物学
结合位点
受体
药理学
生物
生物化学
物理
量子力学
古生物学
作者
David C. Swinney,Brad A. Haubrich,Isabelle Van Liefde,Georges Vauquelin
标识
DOI:10.2174/1568026615666150701113054
摘要
Binding kinetics are the rates of association and dissociation of a drug-protein complex and are important molecular descriptors for the optimization of drug binding to G-protein coupled receptors (GPCRs). There are now many examples of binding kinetics in GPCR drug discovery. In this report, the first principles and examples of binding kinetics in GPCR drug discovery are reviewed. Addressed are the influence of binding kinetics on the translation of binding to the therapeutic window in the context of the equilibrium state of the system and molecular mechanisms of slow binding including induced fit, displacement of water, rebinding and heterovalency.
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