Literature DB >> 31724281

The 3F Library: Fluorinated Fsp3 -Rich Fragments for Expeditious 19 F NMR Based Screening.

Nikolaj S Troelsen1, Elena Shanina2,3, Diego Gonzalez-Romero4, Daniela Danková1, Ida S A Jensen1, Katarzyna J Śniady1, Faranak Nami1, Hengxi Zhang2,3, Christoph Rademacher2,3, Ana Cuenda4, Charlotte H Gotfredsen5, Mads H Clausen1.   

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, Fsp3 -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.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  NMR spectroscopy; drug discovery; fluorine; molecular diversity; synthesis design

Mesh:

Substances:

Year:  2019        PMID: 31724281     DOI: 10.1002/anie.201913125

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  12 in total

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4.  Automated Glycan Assembly of 19 F-labeled Glycan Probes Enables High-Throughput NMR Studies of Protein-Glycan Interactions.

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5.  Design and Synthesis of 56 Shape-Diverse 3D Fragments.

Authors:  Thomas D Downes; S Paul Jones; Hanna F Klein; Mary C Wheldon; Masakazu Atobe; Paul S Bond; James D Firth; Ngai S Chan; Laura Waddelove; Roderick E Hubbard; David C Blakemore; Claudia De Fusco; Stephen D Roughley; Lewis R Vidler; Maria Ann Whatton; Alison J-A Woolford; Gail L Wrigley; Peter O'Brien
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Review 10.  Fragment-based drug discovery: opportunities for organic synthesis.

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