共价片段文库在药物发现中的应用——设计、合成和筛选方法。

Q1 Pharmacology, Toxicology and Pharmaceutics
Progress in medicinal chemistry Pub Date : 2023-01-01 Epub Date: 2023-11-13 DOI:10.1016/bs.pmch.2023.10.003
Brad Hocking, Alan Armstrong, David J Mann
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引用次数: 0

摘要

随着具有共价作用模式的药物的开发越来越受欢迎,经过验证的基于共价片段的药物发现(FBDD)方法相对较慢,无法跟上需求。在本章中,深入探讨了共价片段反应性原理、文库设计、合成和筛选方法,重点介绍了直接应用于实际共价片段文库设计和筛选的文献实例。此外,对该领域的未来进行了探讨,并提出了潜在的有用进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Covalent fragment libraries in drug discovery-Design, synthesis, and screening methods.

As the development of drugs with a covalent mode of action is becoming increasingly popular, well-validated covalent fragment-based drug discovery (FBDD) methods have been comparatively slow to keep up with the demand. In this chapter the principles of covalent fragment reactivity, library design, synthesis, and screening methods are explored in depth, focussing on literature examples with direct applications to practical covalent fragment library design and screening. Further, questions about the future of the field are explored and potential useful advances are proposed.

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来源期刊
Progress in medicinal chemistry
Progress in medicinal chemistry Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
15.60
自引率
0.00%
发文量
6
期刊介绍: This series has a long established reputation for excellent coverage of almost every facet of Medicinal Chemistry and is one of the most respected and instructive sources of information on the subject. The latest volume certifies to the continuing success of a unique series reflecting current progress in a broadly developing field of science.
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