| Literature DB >> 35282568 |
Christian Fischer1, Nynke A Vepřek1,2, Zisis Peitsinis1, Klaus-Peter Rühmann1, Chao Yang1, Jessica N Spradlin3, Dustin Dovala4, Daniel K Nomura3, Yingkai Zhang1, Dirk Trauner1.
Abstract
The COVID-19 pandemic prompted many scientists to investigate remedies against SARS-CoV-2 and related viruses that are likely to appear in the future. As the main protease of the virus, MPro, is highly conserved among coronaviruses, it has emerged as a prime target for developing inhibitors. Using a combination of virtual screening and molecular modeling, we identified small molecules that were easily accessible and could be quickly diversified. Biochemical assays confirmed a class of pyridones as low micromolar non-covalent inhibitors of the viral main protease.Entities:
Keywords: Coronavirus; Molecular Modeling; SARS-CoV-2; Small-Molecule Inhibitor; Viral Main Protease
Year: 2021 PMID: 35282568 PMCID: PMC8916680 DOI: 10.1055/a-1582-0243
Source DB: PubMed Journal: Synlett ISSN: 0936-5214 Impact factor: 2.170