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药物发现中多样性和聚焦组合文库的设计。

Design of diversity and focused combinatorial libraries in drug discovery.

作者信息

Young S Stanley, Ge Nanxiang

机构信息

National Institute of Statistical Science, Research Triangle Park, NC 27709, USA.

出版信息

Curr Opin Drug Discov Devel. 2004 May;7(3):318-24.

Abstract

Using well-characterized chemical reactions and readily available monomers, chemists are able to create sets of compounds, termed libraries, which are useful in drug discovery processes. The design of combinatorial chemical libraries can be complex and there has been much information recently published offering suggestions on how the design process can be carried out. This review focuses on literature with the goal of organizing current thinking. At this point in time, it is clear that benchmarking of current suggested methods is required as opposed to further new methods.

摘要

利用特征明确的化学反应和易于获得的单体,化学家能够创建一系列化合物,称为文库,这些文库在药物发现过程中很有用。组合化学文库的设计可能很复杂,最近有很多信息发表,就如何进行设计过程提供了建议。这篇综述聚焦于相关文献,目的是梳理当前的思路。目前很明显,需要对当前建议的方法进行基准测试,而不是进一步提出新方法。

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