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Eur J Med Chem ; 268: 116263, 2024 Mar 15.
Article in English | MEDLINE | ID: mdl-38432056

ABSTRACT

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and related variants, are responsible for the devastating coronavirus disease 2019 (COVID-19) pandemic. The SARS-CoV-2 main protease (Mpro) plays a central role in the replication of the virus and represents an attractive drug target. Herein, we report the discovery of novel SARS-CoV-2 Mpro covalent inhibitors, including highly effective compound NIP-22c which displays high potency against several key variants and clinically relevant nirmatrelvir Mpro E166V mutants.


Subject(s)
COVID-19 , Peptidomimetics , Humans , Peptidomimetics/pharmacology , Peptide Hydrolases , Protease Inhibitors/pharmacology , SARS-CoV-2 , Cysteine Endopeptidases , Antiviral Agents/pharmacology
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