共价键
生物
一套
鉴定(生物学)
药物发现
计算生物学
化学
计算机科学
电泳剂
组合化学
纳米技术
数据科学
生物化学
生物
政治学
有机化学
材料科学
催化作用
古生物学
植物
自然(考古学)
法学
作者
Simon C. C. Lucas,J. Henry Blackwell,Sarah H. Hewitt,Hannah Semple,Benjamin C. Whitehurst,Hua Xu
标识
DOI:10.1016/j.slasd.2024.01.003
摘要
Covalent hits for drug discovery campaigns are neither fantastic beasts nor mythical creatures, they can be routinely identified through electrophile-first screening campaigns using a suite of different techniques. These include biophysical and biochemical methods, cellular approaches, and DNA-encoded libraries. Employing best practice, however, is critical to success. The purpose of this review is to look at state of the art covalent hit identification, how to identify hits from a covalent library and how to select compounds for medicinal chemistry programmes.
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