| Literature DB >> 32529824 |
Matthew R Bentley1, Olga V Ilyichova1, Geqing Wang2, Martin L Williams1, Gaurav Sharma1, Wesam S Alwan1, Rebecca L Whitehouse1, Biswaranjan Mohanty1,3, Peter J Scammells1, Begoña Heras2, Jennifer L Martin4,5, Makrina Totsika6, Ben Capuano1,3, Bradley C Doak1,3,7, Martin J Scanlon1,3,7.
Abstract
A bottleneck in fragment-based lead development is the lack of systematic approaches to elaborate the initial fragment hits, which usually bind with low affinity to their target. Herein, we describe an analysis using X-ray crystallography of a diverse library of compounds prepared using microscale parallel synthesis. This approach yielded an 8-fold increase in affinity and detailed structural information for the resulting complex, providing an efficient and broadly applicable approach to early fragment development.Mesh:
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Year: 2020 PMID: 32529824 DOI: 10.1021/acs.jmedchem.0c00111
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446