Frontiers in Pharmacology (Jan 2021)

Drug Repurposing Screen for Compounds Inhibiting the Cytopathic Effect of SARS-CoV-2

  • Catherine Z. Chen,
  • Paul Shinn,
  • Zina Itkin,
  • Richard T. Eastman,
  • Robert Bostwick,
  • Lynn Rasmussen,
  • Ruili Huang,
  • Min Shen,
  • Xin Hu,
  • Kelli M. Wilson,
  • Brianna M. Brooks,
  • Hui Guo,
  • Tongan Zhao,
  • Carleen Klump-Thomas,
  • Anton Simeonov,
  • Samuel G. Michael,
  • Donald C. Lo,
  • Matthew D. Hall,
  • Wei Zheng

DOI
https://doi.org/10.3389/fphar.2020.592737
Journal volume & issue
Vol. 11

Abstract

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Drug repurposing is a rapid approach to identify therapeutics for the treatment of emerging infectious diseases such as COVID-19. To address the urgent need for treatment options, we carried out a quantitative high-throughput screen using a SARS-CoV-2 cytopathic assay with a compound collection of 8,810 approved and investigational drugs, mechanism-based bioactive compounds, and natural products. Three hundred and nineteen compounds with anti-SARS-CoV-2 activities were identified and confirmed, including 91 approved drugs and 49 investigational drugs. The anti-SARS-CoV-2 activities of 230 of these confirmed compounds, of which 38 are approved drugs, have not been previously reported. Chlorprothixene, methotrimeprazine, and piperacetazine were the three most potent FDA-approved drugs with anti-SARS-CoV-2 activities. These three compounds have not been previously reported to have anti-SARS-CoV-2 activities, although their antiviral activities against SARS-CoV and Ebola virus have been reported. These results demonstrate that this comprehensive data set is a useful resource for drug repurposing efforts, including design of new drug combinations for clinical trials for SARS-CoV-2.

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