Halogen-enriched fragment libraries as chemical probes for harnessing halogen bonding in fragment-based lead discovery

被引:0
作者
Zimmermann, Markus O. [1 ]
Lange, Andreas [1 ]
Wilcken, Rainer [1 ,2 ,3 ]
Cieslik, Markus B. [1 ]
Exner, Thomas E. [1 ]
Joerger, Andreas C. [2 ]
Koch, Pierre [1 ]
Boeckler, Frank M. [1 ]
机构
[1] Univ Tubingen, Dept Pharmaceut & Med Chem, Inst Pharmaceut Sci, D-72076 Tubingen, Germany
[2] MRC Lab Mol Biol, Cambridge CB2 0QH, England
[3] Novartis Inst BioMed Res, CH-4002 Basel, Switzerland
关键词
CROSS-COUPLING REACTIONS; X-RAY CRYSTALLOGRAPHY; DRUG DISCOVERY; REVERSE-TRANSCRIPTASE; STRUCTURAL BASIS; BINDING-SITES; ORGANOBORON DERIVATIVES; MOLECULAR-INTERACTIONS; MEDICINAL CHEMISTRY; SELECTIVE SYNTHESIS;
D O I
10.4155/FMC.14.20
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Halogen bonding has recently experienced a renaissance, gaining increased recognition as a useful molecular interaction in the life sciences. Halogen bonds are favorable, fairly directional interactions between an electropositive region on the halogen (the sigma-hole) and a number of different nucleophilic interaction partners. Some aspects of halogen bonding are not yet understood well enough to take full advantage of its potential in drug discovery. We describe and present the concept of halogen-enriched fragment libraries. These libraries consist of unique chemical probes, facilitating the identification of favorable halogen bonds by sharing the advantages of classical fragment-based screening. Besides providing insights into the nature and applicability of halogen bonding, halogen-enriched fragment libraries provide smart starting points for hit-to-lead evolution.
引用
收藏
页码:617 / 639
页数:23
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