Advances in the Development of SARS-CoV-2 Mpro Inhibitors

Molecules. 2022 Apr 14;27(8):2523. doi: 10.3390/molecules27082523.

Abstract

Since the outbreak of COVID-19, one of the strategies used to search for new drugs has been to find inhibitors of the main protease (Mpro) of the virus SARS-CoV-2. Initially, previously reported inhibitors of related proteases such as the main proteases of SARS-CoV and MERS-CoV were tested. A huge effort was then carried out by the scientific community to design, synthesize and test new small molecules acting as inactivators of SARS-CoV-2 Mpro. From the chemical structure view, these compounds can be classified into two main groups: one corresponds to modified peptides displaying an adequate sequence for high affinity and a reactive warhead; and the second is a diverse group including chemical compounds that do not have a peptide framework. Although a drug including a SARS-CoV-2 main protease inhibitor has already been commercialized, denoting the importance of this field, more compounds have been demonstrated to be promising potent inhibitors as potential antiviral drugs.

Keywords: COVID-19; Mpro; inhibitors; main protease.

Publication types

  • Review

MeSH terms

  • Antiviral Agents / pharmacology
  • COVID-19 Drug Treatment*
  • Coronavirus 3C Proteases
  • Humans
  • Molecular Docking Simulation
  • Peptide Hydrolases
  • Protease Inhibitors / pharmacology
  • SARS-CoV-2*

Substances

  • Antiviral Agents
  • Protease Inhibitors
  • Peptide Hydrolases
  • 3C-like proteinase, SARS-CoV-2
  • Coronavirus 3C Proteases