Identification of Antiviral Drug Candidates against SARS-CoV-2 from FDA-Approved Drugs
Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral...
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Published in | Antimicrobial agents and chemotherapy Vol. 64; no. 7 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Microbiology
23.06.2020
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Subjects | |
Online Access | Get full text |
ISSN | 0066-4804 1098-6596 1098-6596 |
DOI | 10.1128/AAC.00819-20 |
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Abstract | Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC
50
s), and in particular, two FDA-approved drugs—niclosamide and ciclesonide—were notable in some respects.
Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC
50
s), and in particular, two FDA-approved drugs—niclosamide and ciclesonide—were notable in some respects. |
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AbstractList | Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC50s), and in particular, two FDA-approved drugs—niclosamide and ciclesonide—were notable in some respects. Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC 50 s), and in particular, two FDA-approved drugs—niclosamide and ciclesonide—were notable in some respects. Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC 50 s), and in particular, two FDA-approved drugs—niclosamide and ciclesonide—were notable in some respects. Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC s), and in particular, two FDA-approved drugs-niclosamide and ciclesonide-were notable in some respects. Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC50s), and in particular, two FDA-approved drugs-niclosamide and ciclesonide-were notable in some respects.Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC50s), and in particular, two FDA-approved drugs-niclosamide and ciclesonide-were notable in some respects. |
Author | Lee, Jihye Byun, Soo Young Kim, Seungtaek Park, Soonju Ko, Meehyun Jeon, Sangeun Choi, Inhee Shum, David |
Author_xml | – sequence: 1 givenname: Sangeun surname: Jeon fullname: Jeon, Sangeun organization: Zoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam, South Korea – sequence: 2 givenname: Meehyun surname: Ko fullname: Ko, Meehyun organization: Zoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam, South Korea – sequence: 3 givenname: Jihye surname: Lee fullname: Lee, Jihye organization: Zoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam, South Korea – sequence: 4 givenname: Inhee surname: Choi fullname: Choi, Inhee organization: Medicinal Chemistry, Institut Pasteur Korea, Seongnam, South Korea – sequence: 5 givenname: Soo Young surname: Byun fullname: Byun, Soo Young organization: Screening Discovery Platform, Institut Pasteur Korea, Seongnam, South Korea – sequence: 6 givenname: Soonju surname: Park fullname: Park, Soonju organization: Screening Discovery Platform, Institut Pasteur Korea, Seongnam, South Korea – sequence: 7 givenname: David surname: Shum fullname: Shum, David organization: Screening Discovery Platform, Institut Pasteur Korea, Seongnam, South Korea – sequence: 8 givenname: Seungtaek surname: Kim fullname: Kim, Seungtaek organization: Zoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam, South Korea |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32366720$$D View this record in MEDLINE/PubMed |
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License | Copyright © 2020 American Society for Microbiology. All Rights Reserved. This article is made available via the PMC Open Access Subset for unrestricted noncommercial re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. https://doi.org/10.1128/ASMCopyrightv2 All Rights Reserved. This article is made available via the PMC Open Access Subset for unrestricted noncommercial re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Citation Jeon S, Ko M, Lee J, Choi I, Byun SY, Park S, Shum D, Kim S. 2020. Identification of antiviral drug candidates against SARS-CoV-2 from FDA-approved drugs. Antimicrob Agents Chemother 64:e00819-20. https://doi.org/10.1128/AAC.00819-20. Sangeun Jeon and Meehyun Ko contributed equally to this work. Author order was determined alphabetically. |
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Title | Identification of Antiviral Drug Candidates against SARS-CoV-2 from FDA-Approved Drugs |
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