| Literature DB >> 35943172 |
Mélanie Uguen1, Gemma Davison1, Lukas J Sprenger1, James H Hunter1, Mathew P Martin2, Shannon Turberville2, Jessica E Watt2, Bernard T Golding3, Martin E M Noble2, Hannah L Stewart1, Michael J Waring1.
Abstract
High-throughput screening provides one of the most common ways of finding hit compounds. Lead-like libraries, in particular, provide hits with compatible functional groups and vectors for structural elaboration and physical properties suitable for optimization. Library synthesis approaches can lead to a lack of chemical diversity because they employ parallel derivatization of common building blocks using single reaction types. We address this problem through a "build-couple-transform" paradigm for the generation of lead-like libraries with scaffold diversity. Nineteen transformations of a 4-oxo-2-butenamide scaffold template were optimized, including 1,4-cyclizations, 3,4-cyclizations, reductions, and 1,4-additions. A pool-transformation approach efficiently explored the scope of these transformations for nine different building blocks and synthesized a >170-member library with enhanced chemical space coverage and favorable drug-like properties. Screening revealed hits against CDK2. This work establishes the build-couple-transform concept for the synthesis of lead-like libraries and provides a differentiated approach to libraries with significantly enhanced scaffold diversity.Entities:
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Year: 2022 PMID: 35943172 PMCID: PMC9421646 DOI: 10.1021/acs.jmedchem.2c00897
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 8.039