Simon C.C. Lucas , J. Henry Blackwell , Sarah H. Hewitt , Hannah Semple , Benjamin C. Whitehurst , Hua Xu
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引用次数: 0
摘要
药物发现活动中的共价化合物既不是神奇的野兽,也不是神话中的生物,它们可以通过亲电子先筛选活动,利用一系列不同的技术进行常规鉴定。这些技术包括生物物理和生物化学方法、细胞方法和 DNA 编码库。然而,采用最佳实践是成功的关键。本综述的目的是介绍最先进的共价反应识别技术、如何从共价化合物库中识别反应,以及如何为药物化学项目选择化合物。
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.