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Bepridil is potent against SARS-CoV-2 in vitro
Guided by a computational docking analysis, about 30 Food and Drug Administration/European Medicines Agency (FDA/EMA)-approved small-molecule medicines were characterized on their inhibition of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (M(p)(ro)). Of these small...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7958448/ https://www.ncbi.nlm.nih.gov/pubmed/33597253 http://dx.doi.org/10.1073/pnas.2012201118 |
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author | Vatansever, Erol C. Yang, Kai S. Drelich, Aleksandra K. Kratch, Kaci C. Cho, Chia-Chuan Kempaiah, Kempaiah Rayavara Hsu, Jason C. Mellott, Drake M. Xu, Shiqing Tseng, Chien-Te K. Liu, Wenshe Ray |
author_facet | Vatansever, Erol C. Yang, Kai S. Drelich, Aleksandra K. Kratch, Kaci C. Cho, Chia-Chuan Kempaiah, Kempaiah Rayavara Hsu, Jason C. Mellott, Drake M. Xu, Shiqing Tseng, Chien-Te K. Liu, Wenshe Ray |
author_sort | Vatansever, Erol C. |
collection | PubMed |
description | Guided by a computational docking analysis, about 30 Food and Drug Administration/European Medicines Agency (FDA/EMA)-approved small-molecule medicines were characterized on their inhibition of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (M(p)(ro)). Of these small molecules tested, six displayed a concentration that inhibits response by 50% (IC(50)) value below 100 μM in inhibiting M(p)(ro), and, importantly, three, that is, pimozide, ebastine, and bepridil, are basic molecules that potentiate dual functions by both raising endosomal pH to interfere with SARS-CoV-2 entry into the human cell host and inhibiting M(p)(ro) in infected cells. A live virus-based modified microneutralization assay revealed that bepridil possesses significant anti−SARS-CoV-2 activity in both Vero E6 and A459/ACE2 cells in a dose-dependent manner with low micromolar effective concentration, 50% (EC(50)) values. Therefore, the current study urges serious considerations of using bepridil in COVID-19 clinical tests. |
format | Online Article Text |
id | pubmed-7958448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-79584482021-03-19 Bepridil is potent against SARS-CoV-2 in vitro Vatansever, Erol C. Yang, Kai S. Drelich, Aleksandra K. Kratch, Kaci C. Cho, Chia-Chuan Kempaiah, Kempaiah Rayavara Hsu, Jason C. Mellott, Drake M. Xu, Shiqing Tseng, Chien-Te K. Liu, Wenshe Ray Proc Natl Acad Sci U S A Biological Sciences Guided by a computational docking analysis, about 30 Food and Drug Administration/European Medicines Agency (FDA/EMA)-approved small-molecule medicines were characterized on their inhibition of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (M(p)(ro)). Of these small molecules tested, six displayed a concentration that inhibits response by 50% (IC(50)) value below 100 μM in inhibiting M(p)(ro), and, importantly, three, that is, pimozide, ebastine, and bepridil, are basic molecules that potentiate dual functions by both raising endosomal pH to interfere with SARS-CoV-2 entry into the human cell host and inhibiting M(p)(ro) in infected cells. A live virus-based modified microneutralization assay revealed that bepridil possesses significant anti−SARS-CoV-2 activity in both Vero E6 and A459/ACE2 cells in a dose-dependent manner with low micromolar effective concentration, 50% (EC(50)) values. Therefore, the current study urges serious considerations of using bepridil in COVID-19 clinical tests. National Academy of Sciences 2021-03-09 2021-02-17 /pmc/articles/PMC7958448/ /pubmed/33597253 http://dx.doi.org/10.1073/pnas.2012201118 Text en Copyright © 2021 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biological Sciences Vatansever, Erol C. Yang, Kai S. Drelich, Aleksandra K. Kratch, Kaci C. Cho, Chia-Chuan Kempaiah, Kempaiah Rayavara Hsu, Jason C. Mellott, Drake M. Xu, Shiqing Tseng, Chien-Te K. Liu, Wenshe Ray Bepridil is potent against SARS-CoV-2 in vitro |
title | Bepridil is potent against SARS-CoV-2 in vitro |
title_full | Bepridil is potent against SARS-CoV-2 in vitro |
title_fullStr | Bepridil is potent against SARS-CoV-2 in vitro |
title_full_unstemmed | Bepridil is potent against SARS-CoV-2 in vitro |
title_short | Bepridil is potent against SARS-CoV-2 in vitro |
title_sort | bepridil is potent against sars-cov-2 in vitro |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7958448/ https://www.ncbi.nlm.nih.gov/pubmed/33597253 http://dx.doi.org/10.1073/pnas.2012201118 |
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