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A Small Molecule That In Vitro Neutralizes Infection of SARS-CoV-2 and Its Most Infectious Variants, Delta, and Omicron
The COVID-19 pandemic has underscored the urgent need to develop highly potent and safe medications that are complementary to the role of vaccines. Specifically, it has exhibited the need for orally bioavailable broad-spectrum antivirals that are able to be quickly deployed against newly emerging vi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10046252/ https://www.ncbi.nlm.nih.gov/pubmed/36979895 http://dx.doi.org/10.3390/biomedicines11030916 |
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author | Reyes-Alcaraz, Arfaxad Qasim, Hanan Merlinsky, Elizabeth Fox, Glenn Islam, Tasneem Medina, Bryan Schwartz, Robert J. Craft, John W. McConnell, Bradley K. |
author_facet | Reyes-Alcaraz, Arfaxad Qasim, Hanan Merlinsky, Elizabeth Fox, Glenn Islam, Tasneem Medina, Bryan Schwartz, Robert J. Craft, John W. McConnell, Bradley K. |
author_sort | Reyes-Alcaraz, Arfaxad |
collection | PubMed |
description | The COVID-19 pandemic has underscored the urgent need to develop highly potent and safe medications that are complementary to the role of vaccines. Specifically, it has exhibited the need for orally bioavailable broad-spectrum antivirals that are able to be quickly deployed against newly emerging viral pathogens. The Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2) and its variants Delta and Omicron are still a major threat to patients of all ages. In this brief report, we describe that the small molecule CD04872SC was able to neutralize SARS-CoV2 infection with a half-maximal effective concentration (EC50) = 248 μM. Serendipitously, we also were able to observe that CD04872SC inhibited the infection of the SARS-CoV-2 variants; Delta (EC50 = 152 μM) and Omicron (EC50 = 308 μM). These properties may define CD04872SC as a potential broad-spectrum candidate lead for the development of treatments for COVID-19. |
format | Online Article Text |
id | pubmed-10046252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100462522023-03-29 A Small Molecule That In Vitro Neutralizes Infection of SARS-CoV-2 and Its Most Infectious Variants, Delta, and Omicron Reyes-Alcaraz, Arfaxad Qasim, Hanan Merlinsky, Elizabeth Fox, Glenn Islam, Tasneem Medina, Bryan Schwartz, Robert J. Craft, John W. McConnell, Bradley K. Biomedicines Brief Report The COVID-19 pandemic has underscored the urgent need to develop highly potent and safe medications that are complementary to the role of vaccines. Specifically, it has exhibited the need for orally bioavailable broad-spectrum antivirals that are able to be quickly deployed against newly emerging viral pathogens. The Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2) and its variants Delta and Omicron are still a major threat to patients of all ages. In this brief report, we describe that the small molecule CD04872SC was able to neutralize SARS-CoV2 infection with a half-maximal effective concentration (EC50) = 248 μM. Serendipitously, we also were able to observe that CD04872SC inhibited the infection of the SARS-CoV-2 variants; Delta (EC50 = 152 μM) and Omicron (EC50 = 308 μM). These properties may define CD04872SC as a potential broad-spectrum candidate lead for the development of treatments for COVID-19. MDPI 2023-03-15 /pmc/articles/PMC10046252/ /pubmed/36979895 http://dx.doi.org/10.3390/biomedicines11030916 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Brief Report Reyes-Alcaraz, Arfaxad Qasim, Hanan Merlinsky, Elizabeth Fox, Glenn Islam, Tasneem Medina, Bryan Schwartz, Robert J. Craft, John W. McConnell, Bradley K. A Small Molecule That In Vitro Neutralizes Infection of SARS-CoV-2 and Its Most Infectious Variants, Delta, and Omicron |
title | A Small Molecule That In Vitro Neutralizes Infection of SARS-CoV-2 and Its Most Infectious Variants, Delta, and Omicron |
title_full | A Small Molecule That In Vitro Neutralizes Infection of SARS-CoV-2 and Its Most Infectious Variants, Delta, and Omicron |
title_fullStr | A Small Molecule That In Vitro Neutralizes Infection of SARS-CoV-2 and Its Most Infectious Variants, Delta, and Omicron |
title_full_unstemmed | A Small Molecule That In Vitro Neutralizes Infection of SARS-CoV-2 and Its Most Infectious Variants, Delta, and Omicron |
title_short | A Small Molecule That In Vitro Neutralizes Infection of SARS-CoV-2 and Its Most Infectious Variants, Delta, and Omicron |
title_sort | small molecule that in vitro neutralizes infection of sars-cov-2 and its most infectious variants, delta, and omicron |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10046252/ https://www.ncbi.nlm.nih.gov/pubmed/36979895 http://dx.doi.org/10.3390/biomedicines11030916 |
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