University of Cambridge, Department of Chemistry, Lensfield Road, Cambridge, United Kingdom CB2 1EW.
Chem Soc Rev. 2012 Jun 21;41(12):4444-56. doi: 10.1039/c2cs35023h. Epub 2012 Apr 10.
Small molecule modulators of biological function can be discovered by the screening of compound libraries. However, it became apparent that some human disease related targets could not be addressed by the libraries commonly used which typically are comprised of large numbers of structurally similar compounds. The last decade has seen a paradigm shift in library construction, with particular emphasis now being placed on increasing a library's structural, and thus functional diversity, rather than only its size. Diversity-oriented synthesis (DOS) aims to generate such structural diversity efficiently. This tutorial review has been written to introduce the subject to a broad audience and recent achievements in both the preparation and the screening of structurally diverse compound collections against so-called 'undruggable' targets are highlighted.
小分子生物功能调节剂可以通过化合物库的筛选来发现。然而,人们逐渐发现,一些与人类疾病相关的靶点无法通过常用的化合物库来解决,这些化合物库通常包含大量结构相似的化合物。在过去的十年中,化合物库的构建方式发生了重大转变,现在的重点是增加化合物库的结构多样性,从而提高其功能多样性,而不仅仅是其规模。多样性导向合成(DOS)旨在有效地产生这种结构多样性。本教程综述的目的是向广大读者介绍这一主题,并重点介绍在针对所谓的“不可成药”靶点的结构多样化合物库的制备和筛选方面的最新进展。