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α-Ketoamides-based covalent inhibitors in drug discovery: Current status and synthetic methods
Ho Ying Huang1, Nicolas Moitessier1
1Department of Chemistry, McGill University, 801 Sherbrooke St. W., Montréal, Québec, H3A 0B8, Canada.
Abstract:
The α-ketoamide moiety is abundant in natural products and has been incorporated by medicinal chemists into novel potential drug candidates. A variety of synthetic methods for preparing this privileged functional group have been disclosed. In this review, we will provide insights into the chemical reactivity of α-ketoamides, their successful incorporation into potent covalent inhibitors and an overview of the synthetic methodologies that are actively used in the discovery of small molecule α-ketoamide covalent inhibitors. Finally, this perspective aims to help medicinal chemists in overcoming synthetic challenges when introducing α-ketoamide groups into more efficient hit/lead molecules, and to highlight the popularity of α-ketoamide in drug design and development.
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