Next generation diversity-oriented synthesis: a paradigm shift from chemical diversity to biological diversity

被引:38
|
作者
Pavlinov, Ivan [1 ]
Gerlach, Erica M. [1 ]
Aldrich, Leslie N. [1 ]
机构
[1] Univ Illinois, Dept Chem, 845 West Taylor St, Chicago, IL 60607 USA
关键词
HIGH-THROUGHPUT EXPERIMENTATION; SMALL MOLECULES; DRUG DISCOVERY; BIOACTIVE COMPOUNDS; CONNECTIVITY MAP; RING-DISTORTION; LIBRARIES; MECHANISM; CYTOTOXICITY; STRATEGY;
D O I
10.1039/c8ob02327a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Diversity-oriented synthesis has historically focused on the generation of small-molecule collections with considerable scaffold, stereochemical, and appendage diversity. Recently, this focus has begun to shift to the production of small-molecule libraries with diverse biological activities. It is currently not clear which properties and structural features of molecules are predictive of diverse performance in biological assays, and a better understanding of this relationship is critical for the development of performance-diverse small-molecule libraries for the discovery of novel probes for challenging targets. This review explores recent synthetic strategies for the production of bioactive small molecules and concludes with a presentation of current methods that enable the assessment of the biological performance diversity of smallmolecule libraries.
引用
收藏
页码:1608 / 1623
页数:16
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