虚拟筛选
共价键
合理设计
药物发现
药品
共价结合
生物信息学
计算生物学
药物靶点
药物设计
抗药性
化学
药理学
组合化学
纳米技术
医学
生物
生物化学
遗传学
材料科学
基因
有机化学
作者
Adebayo A. Adeniyi,Ramesh Muthusamy,Mahmoud E. S. Soliman
标识
DOI:10.1517/17460441.2016.1115478
摘要
A major challenge for drug design is the alarming increase in drug resistance, mutations and toxicity. In recent years, covalent drugs have become a promising option to address these problems, due to their significant advantages. These advantages include their ability to target rare, non-conserved residues, shallow binding sites of target proteins and their ability to retain their binding with a receptor for a very long time.This review shows the increasing progress in rational design and virtual screening of covalent drugs and the promising future of accurately predicting effective covalent drugs through in silico screening.All the current clinically approved covalent drugs were discovered by chance instead of systematic design. There is a promising and commendable effort towards high-throughput screening and the accurate discovery of new covalent inhibitors, which may address the problems of drug resistance and mutation. However, despite the current progression, there is still a need for more rational attention to improve the covalent warhead for improved receptor interaction and selectivity.
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