Overview of Targets and Potential Drugs of SARS-CoV-2 According to the Viral Replication

J Proteome Res. 2021 Jan 1;20(1):49-59. doi: 10.1021/acs.jproteome.0c00526. Epub 2020 Dec 21.

Abstract

Since the novel coronavirus pandemic, people around the world have been touched in varying degrees, and this pandemic has raised a major global health concern. As there is no effective drug or vaccine, it is urgent to find therapeutic drugs that can serve to deal with the current epidemic situation in all countries and regions. We searched drugs and response measures for SARS-CoV-2 in the PubMed database, and then updated the potential targets and therapeutic drugs from the perspective of the viral replication cycle. The drug research studies of the viral replication cycle are predominantly focused on the process of the virus entering cells, proteases, and RdRp. The inhibitors of the virus entry to cells and RdRp, such as Arbidol, remdesivir, favipiravir, EIDD-2081, and ribavirin, are in clinical trials, while most of the protease inhibitors are mainly calculated by molecular docking technology, which needs in vivo and in vitro experiments to prove the effect for SARS-CoV-2. This review summarizes the drugs targeting the viral replication process and provides a basis and directions for future drug development and reuse on the protein level of COVID-19.

Keywords: SARS-CoV-2; drug; replication process; target.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Angiotensin-Converting Enzyme 2 / metabolism
  • Animals
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Basigin / metabolism
  • Coronavirus 3C Proteases / antagonists & inhibitors
  • Coronavirus 3C Proteases / metabolism
  • Coronavirus Nucleocapsid Proteins / chemistry
  • Coronavirus Nucleocapsid Proteins / metabolism
  • Coronavirus RNA-Dependent RNA Polymerase / metabolism
  • Dipeptidyl Peptidase 4 / metabolism
  • Furin / antagonists & inhibitors
  • Furin / metabolism
  • Host-Pathogen Interactions / drug effects
  • Humans
  • SARS-CoV-2 / drug effects*
  • SARS-CoV-2 / pathogenicity
  • SARS-CoV-2 / physiology
  • Serine Endopeptidases / metabolism
  • Small Molecule Libraries / pharmacology
  • Spike Glycoprotein, Coronavirus / chemistry
  • Spike Glycoprotein, Coronavirus / metabolism
  • Virus Replication / drug effects*

Substances

  • Antiviral Agents
  • BSG protein, human
  • Coronavirus Nucleocapsid Proteins
  • Small Molecule Libraries
  • Spike Glycoprotein, Coronavirus
  • spike protein, SARS-CoV-2
  • Basigin
  • Coronavirus RNA-Dependent RNA Polymerase
  • NSP12 protein, SARS-CoV-2
  • DPP4 protein, human
  • Dipeptidyl Peptidase 4
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2
  • Serine Endopeptidases
  • TMPRSS2 protein, human
  • FURIN protein, human
  • Furin
  • Coronavirus 3C Proteases