| Literature DB >> 33708112 |
Catherine Z Chen1, Paul Shinn1, Zina Itkin1, Richard T Eastman1, Robert Bostwick2, Lynn Rasmussen2, Ruili Huang1, Min Shen1, Xin Hu1, Kelli M Wilson1, Brianna M Brooks1, Hui Guo1, Tongan Zhao1, Carleen Klump-Thomas1, Anton Simeonov1, Samuel G Michael1, Donald C Lo1, Matthew D Hall1, Wei Zheng1.
Abstract
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.Entities:
Keywords: COVID-19; HTS; SARS-CoV-2; cytopathic effect; drug repurposing and discovery
Year: 2021 PMID: 33708112 PMCID: PMC7942396 DOI: 10.3389/fphar.2020.592737
Source DB: PubMed Journal: Front Pharmacol ISSN: 1663-9812 Impact factor: 5.810