药物发现
配体效率
药物设计
合理设计
药品
化学
计算生物学
配体(生物化学)
组合化学
立体化学
计算机科学
纳米技术
药理学
生物化学
生物
材料科学
受体
作者
Zengjun Fang,Yuning Song,Peng Zhan,Qingzhu Zhang,Xinyong Liu
摘要
The conformational restriction (rigidification) of a flexible ligand has often been a commonly used strategy in drug design, as it can minimize the entropic loss associated with the ligand adopting a preferred conformation for binding, which leads to enhanced potency for a given physiological target, improved selectivity for isoforms and reduced the possibility of drug metabolism. Therefore, the application of conformational restriction strategy is a core aspect of drug discovery and development that is widely practiced by medicinal chemists either deliberately or subliminally. The present review will highlight current representative examples and a brief overview on the rational design of conformationally restricted agents as well as discuss its advantages over the flexible counterparts.
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