Dynamic Combinatorial Chemistry: A New Methodology Comes of Age

被引:86
作者
Frei, Priska [1 ]
Hevey, Rachel [1 ]
Ernst, Beat [1 ]
机构
[1] Univ Basel, Inst Mol Pharm, Pharmactr, Klingelbergstr 50, CH-4056 Basel, Switzerland
关键词
drug discovery; dynamic combinatorial chemistry; host-guest systems; supramolecular chemistry; target-directed dynamic combinatorial chemistry; ASPARTIC PROTEASE ENDOTHIAPEPSIN; BETA-GALACTOSIDASE INHIBITORS; MASS-SPECTROMETRY LEADS; NEURAMINIDASE INHIBITORS; SUPRAMOLECULAR CHEMISTRY; NUCLEOPHILIC CATALYSIS; MOLECULAR RECOGNITION; DISULFIDE EXCHANGE; CHEMICAL-BIOLOGY; CLICK CHEMISTRY;
D O I
10.1002/chem.201803365
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dynamic combinatorial chemistry (DCC) has repeatedly proven to be an effective approach to generate directed ligand libraries for macromolecular targets. In the absence of an external stimulus, a dynamic library forms from reversibly reacting building blocks and reaches a stable thermodynamic equilibrium. However, upon addition of a macromolecular host which can bind and stabilize certain components of the library, the equilibrium composition changes and induces an evolution-like selection and enrichment of high-affinity ligands. A valuable application of this so-called target-directed DCC (tdDCC) is the identification of potent ligands for pharmacologically relevant targets. Over time, the term tdDCC has been applied to describe a number of different experimental setups, leading to some ambiguity concerning its definition. This article systematically classifies known procedures for tdDCC and related approaches, with a special focus on the methods used for analysis and evaluation of experiments.
引用
收藏
页码:60 / 73
页数:14
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