Magee Thomas V
Worldwide Medicinal Chemistry, Pfizer Inc, 610 Main Street, Cambridge, MA 02139, USA.
Bioorg Med Chem Lett. 2015 Jun 15;25(12):2461-8. doi: 10.1016/j.bmcl.2015.04.089. Epub 2015 May 2.
Protein-protein interactions (PPIs) present a formidable challenge to medicinal chemistry. The extended and open nature of many binding sites at protein interfaces has made it difficult to find useful chemical matter by traditional screening methods using standard screening libraries. This Digest focuses on the progress that has been made in discovering small-molecule modulators for a diverse selection of PPI targets using fragment screening and highlights the utility of this strategy in this context.
蛋白质-蛋白质相互作用(PPIs)给药物化学带来了巨大挑战。蛋白质界面上许多结合位点具有延伸性和开放性,这使得利用传统筛选方法和标准筛选文库来寻找有用的化学物质变得困难。本综述聚焦于通过片段筛选发现多种PPI靶点的小分子调节剂所取得的进展,并突出了该策略在此背景下的实用性。