Kinetic target-guided synthesis in drug discovery and chemical biology: a comprehensive facts and figures survey

被引:29
|
作者
Bosc, Damien [1 ]
Jakhlal, Jouda [1 ]
Deprez, Benoit [1 ]
Deprez-Poulain, Rebecca [1 ]
机构
[1] Univ Lille, INSERM, Inst Pasteur Lille, Drugs & Mol Living Syst U1177, F-59000 Lille, France
关键词
SITU CLICK-CHEMISTRY; PROTEIN-CAPTURE AGENTS; CARBONIC-ANHYDRASE-II; IN-SITU; ACETYLCHOLINESTERASE INHIBITORS; SELECTIVE INHIBITOR; TERMINAL ALKYNES; ACHE INHIBITORS; THIO ACIDS; AZIDES;
D O I
10.4155/fmc-2015-0007
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
For the last 15 years, kinetic target-guided syntheses, including in situ click chemistry, have been used as alternative methods to find ligands to therapeutically relevant proteins. In this review, a comprehensive survey of biological targets used in kinetic target-guided synthesis covers historical and recent examples. The chemical reactions employed and practical aspects, including controls, library sizes and product detection, are presented. A particular focus is on the reagents and warhead selection and design with a critical overview of the challenges encountered. As protein supply remains a key success factor, it appears that increased efforts should be taken toward miniaturization in order to expand the scope of this strategy and qualify it as a fully fledged drug discovery tool.
引用
收藏
页码:381 / 404
页数:24
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