张磊, 郑明月, 柳红. 多样性合成及其在药物发现中的应用J. 药学学报, 2015,50(4): 419-433.
引用本文: 张磊, 郑明月, 柳红. 多样性合成及其在药物发现中的应用J. 药学学报, 2015,50(4): 419-433.
ZHANG Lei, ZHENG Ming-yue, LIU Hong. Diversity-oriented synthesis and its application in drug discoveryJ. Acta Pharmaceutica Sinica, 2015,50(4): 419-433.
Citation: ZHANG Lei, ZHENG Ming-yue, LIU Hong. Diversity-oriented synthesis and its application in drug discoveryJ. Acta Pharmaceutica Sinica, 2015,50(4): 419-433.

多样性合成及其在药物发现中的应用

Diversity-oriented synthesis and its application in drug discovery

  • 摘要: 多样性合成旨在高效地构建取代基、官能团、立体化学和骨架多样的化合物库,进而发现多样性的生物学效应.本文结合代表性实例,总结了多样性合成的常见策略,包括基于试剂的策略、基于底物的策略、“构建-耦合-配对”策略以及基于优势结构的多样性合成策略.同时,介绍了通过多样性合成构建的化合物库在药物发现中的应用.

     

    Abstract: Diversity-oriented synthesis (DOS) aims to efficiently generate collections of small molecules with diverse appendages, functional groups, stereochemistry and skeletons, thus yielding diverse biological activities capable of modulating a wide variety of biological processes. In this review, we discussed the common strategies employed in DOS with specific examples from recent literature, including reagent-based approach, substrate-based approach, build-couple-pair strategy and privileged substructure-based DOS. The application of some DOS libraries in drug discovery is also presented.

     

/

返回文章
返回