片段(逻辑)
工作流程
组合化学
药物发现
化学
核磁共振波谱
计算机科学
纳米技术
立体化学
材料科学
数据库
生物化学
程序设计语言
作者
Nikolaj S. Troelsen,Elena Shanina,Diego González‐Romero,Daniela Danková,Ida S. A. Jensen,Katarzyna J. Śniady,Faranak Nami,Hengxi Zhang,Christoph Rademacher,Ana Cuenda,Charlotte H. Gotfredsen,Mads H. Clausen
标识
DOI:10.1002/anie.201913125
摘要
Abstract Fragment‐based drug discovery (FBDD) is a popular method in academia and the pharmaceutical industry for the discovery of early lead candidates. Despite its wide‐spread use, the approach still suffers from laborious screening workflows and a limited diversity in the fragments applied. Presented here is the design, synthesis, and biological evaluation of the first fragment library specifically tailored to tackle both these challenges. The 3F library of 115 fluorinated, Fsp 3 ‐rich fragments is shape diverse and natural‐product‐like with desirable physicochemical properties. The library is perfectly suited for rapid and efficient screening by NMR spectroscopy in a two‐stage workflow of 19 F NMR and subsequent 1 H NMR methods. Hits against four diverse protein targets are widely distributed among the fragment scaffolds in the 3F library and a 67 % validation rate was achieved using secondary assays. This collection is the first synthetic fragment library tailor‐made for 19 F NMR screening and the results demonstrate that the approach should find broad application in the FBDD community.
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