Dynamic combinatorial chemistry: a tool to facilitate the identification of inhibitors for protein targets

被引:170
作者
Mondal, Milon [1 ]
Hirsch, Anna K. H. [1 ]
机构
[1] Univ Groningen, Stratingh Inst Chem, NL-9747 AG Groningen, Netherlands
关键词
CYCLIN-DEPENDENT KINASES; MASS-SPECTROMETRY LEADS; MS-BINDING ASSAYS; DRUG DISCOVERY; COVALENT CHEMISTRY; MOLECULAR RECOGNITION; OXYGENASE INHIBITORS; GLUTATHIONE ANALOGS; HYDROLYTIC ACTIVITY; ALPHA-CHYMOTRYPSIN;
D O I
10.1039/c4cs00493k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dynamic combinatorial chemistry (DCC) has emerged as a powerful strategy to identify ligands for biological targets given that it enables the target to direct the synthesis and amplification of its strongest binder(s) from the library of interconverting compounds. Since the first report of DCC applied to the discovery of binders for a protein, this elegant tool has been employed on a range of protein targets at various stages of medicinal-chemistry projects. A series of suitable, reversible reactions that are biocompatible have been established and the portfolio of analytical techniques is growing. Despite progress, in most cases, the libraries employed remain of moderate size. We present here the most recent advances in the field of DCC applied to protein targets, paying particular attention to the experimental conditions and analytical methods chosen.
引用
收藏
页码:2455 / 2488
页数:34
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