Natural product-like synthetic libraries

被引:75
作者
Thomas, Gemma L. [1 ]
Johannes, Charles W. [1 ]
机构
[1] Inst Chem & Engn Sci, Singapore 138667, Singapore
关键词
DIVERSITY-ORIENTED SYNTHESIS; DRUG DISCOVERY; SKELETAL DIVERSITY; ONE-POT; MOLECULES; STRATEGY; ANALOGS;
D O I
10.1016/j.cbpa.2011.05.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is a paucity of chemical matter suitably poised for effective drug development. Improving the quality and efficiency of research early on in the drug discovery process has been a long standing objective for the drug industry and improvements to the accessibility and quality of compound screening decks might have a significant and positive impact. In the absence of specific molecular information that can be modeled and used predicatively we are far from identifying which small molecules are most relevant to emerging biological targets such as protein protein interactions. Natural products have been historically successful as an entry point for drug discovery and recently screening libraries are being synthesized to emulate natural product like features.
引用
收藏
页码:516 / 522
页数:7
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