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生物系统用化学探针

Chemical probes for biological systems.

机构信息

Chemogenomics Laboratory, Research Program on Biomedical Informatics (GRIB), Institut Municipal d'Investigació Mèdica and Universitat Pompeu Fabra, Parc de Recerca Biomèdica, Doctor Aiguader 88, 08003 Barcelona, Catalonia, Spain.

出版信息

Drug Discov Today. 2011 Feb;16(3-4):99-106. doi: 10.1016/j.drudis.2010.11.004. Epub 2010 Nov 18.

Abstract

According to the latest definition in use by the NIH Molecular Libraries Screening Centers Network, a compound to be nominated as a chemical probe should have, on the one hand, an affinity below 100 nM for the primary target and, on the other hand, at least tenfold selectivity against related targets. Taking drugs as the ultimate product of an affinity and selectivity optimization process, it is found that only 14.4% of them would actually qualify as chemical probes under those criteria. Therefore, if chemical probes are expected to give rise to new medicines, strict adherence to the current probe definition might result in many compounds of potential therapeutic interest being overlooked.

摘要

根据 NIH 分子库筛选中心网络目前使用的最新定义,一种被提名的化学探针化合物,一方面应该对主要靶标具有低于 100 nM 的亲和力,另一方面,对相关靶标至少要有十倍的选择性。考虑到药物是亲和力和选择性优化过程的最终产物,可以发现,只有 14.4%的药物实际上符合这些标准,可以被认为是化学探针。因此,如果化学探针有望产生新药,严格遵守当前的探针定义可能会导致许多具有潜在治疗意义的化合物被忽视。

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