当前平行化学原理与实践:在发现生物活性分子中的应用。

Paul J Edwards
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引用次数: 0

摘要

本文基于2006年1月至2008年12月的出版物,描述了平行化学技术在药物发现中的应用。在一系列生物靶标中产生活性化合物的化学文库,以及适当的合成细节。还讨论了所涉及的生物靶点的背景信息以及在库系列成员中可以识别的任何SAR。新技术的发展,如应用于图书馆的设计和合成,更一般地说,在生物活性实体的发现,强调。此外,平行化学在其影响药物发现的能力方面可能的未来方向也被提出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current parallel chemistry principles and practice: application to the discovery of biologically active molecules.

This article describes the use of parallel chemistry techniques for drug discovery, based on publications from January 2006 to December 2008. Chemical libraries that yielded active compounds across a range of biological targets are presented, together with synthetic details when appropriate. Background information for the biological targets involved and any SAR that could be discerned within members of a library series also is discussed. New technological developments, as applied to library design and synthesis and, more generally, in the discovery of biologically active entities, are highlighted. In addition, the likely future directions for parallel chemistry in its ability to impact upon drug discovery are also presented.

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