动力学
受体-配体动力学
药物发现
计算生物学
化学
酶动力学
药品
生物物理学
生物
生物化学
药理学
物理
酶
量子力学
活动站点
作者
Dong Guo,Laura H. Heitman,Adriaan P. IJzerman
出处
期刊:ChemMedChem
[Wiley]
日期:2015-08-25
卷期号:10 (11): 1793-1796
被引量:46
标识
DOI:10.1002/cmdc.201500310
摘要
Abstract Traditionally structure–activity/affinity relationships (SAR) have dominated research in medicinal chemistry. However, structure–kinetics relationships (SKR) can be very informative too. In this viewpoint we explore the molecular determinants of binding kinetics and discuss challenges for future binding kinetics studies. A scheme for future kinetics‐directed drug design and discovery is also proposed.
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