Nefzi Adel, Ostresh John M, Yu Yongping, Houghten Richard A
Torrey Pines Institute for Molecular Studies, 3550 General Atomics Court, San Diego, California 92121, USA.
J Org Chem. 2004 May 28;69(11):3603-9. doi: 10.1021/jo040114j.
Combinatorial chemistry has deeply impacted the drug discovery process by accelerating the synthesis and screening of large numbers of compounds having therapeutic and/or diagnostic potential. These techniques offer unique enhancement in the potential identification of new and/or therapeutic candidates. Our efforts over the past 10 years in the design and diversity-oriented synthesis of low molecular weight acyclic and heterocyclic combinatorial libraries derived from amino acids, peptides, and/or peptidomimetics are described. Employing a "toolbox" of various chemical transformations, including alkylation, oxidation, reduction, acylation, and the use of a variety of multifunctional reagents, the "libraries from libraries" concept has enabled the continued development of an ever-expanding, structurally varied series of organic chemical libraries.
组合化学通过加速对大量具有治疗和/或诊断潜力的化合物的合成与筛选,对药物发现过程产生了深远影响。这些技术在潜在新的和/或治疗候选物的识别方面提供了独特的增强作用。本文描述了我们在过去10年中,从氨基酸、肽和/或拟肽设计并以多样性为导向合成低分子量无环和杂环组合文库的工作。利用包括烷基化、氧化、还原、酰化等各种化学转化的“工具箱”,以及使用各种多功能试剂,“文库之文库”的概念使得一系列不断扩展、结构多样的有机化学文库得以持续发展。