Drug repurposing against SARS-CoV-1, SARS-CoV-2 and MERS-CoV

Future Microbiol. 2021 Nov:16:1341-1370. doi: 10.2217/fmb-2021-0019. Epub 2021 Nov 10.

Abstract

Since the beginning of the COVID-19 pandemic, large in silico screening studies and numerous in vitro studies have assessed the antiviral activity of various drugs on SARS-CoV-2. In the context of health emergency, drug repurposing represents the most relevant strategy because of the reduced time for approval by international medicines agencies, the low cost of development and the well-known toxicity profile of such drugs. Herein, we aim to review drugs with in vitro antiviral activity against SARS-CoV-2, combined with molecular docking data and results from preliminary clinical studies. Finally, when considering all these previous findings, as well as the possibility of oral administration, 11 molecules consisting of nelfinavir, favipiravir, azithromycin, clofoctol, clofazimine, ivermectin, nitazoxanide, amodiaquine, heparin, chloroquine and hydroxychloroquine, show an interesting antiviral activity that could be exploited as possible drug candidates for COVID-19 treatment.

Keywords: COVID-19; SARS-CoV-1; SARS-CoV-2; antiviral; coronavirus; drug repurposing; in silico; in vitro testing.

MeSH terms

  • Animals
  • Antiviral Agents / therapeutic use*
  • COVID-19 / virology
  • COVID-19 Drug Treatment*
  • Cell Line
  • Chlorocebus aethiops
  • Drug Repositioning / methods
  • Humans
  • Middle East Respiratory Syndrome Coronavirus / drug effects*
  • Molecular Docking Simulation
  • Pandemics / prevention & control
  • SARS-CoV-2 / drug effects*
  • Vero Cells

Substances

  • Antiviral Agents