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Discovery of cyclic sulfonamide derivatives as potent inhibitors of SARS-CoV-2
Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) continues to spread worldwide, with 25 million confirmed cases and 800 thousand deaths. Effective treatments to target SARS-CoV-2 are urgently needed. In the present study, we have identified a class of cyclic sulfonamide derivatives as no...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7640924/ https://www.ncbi.nlm.nih.gov/pubmed/33160024 http://dx.doi.org/10.1016/j.bmcl.2020.127667 |
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author | Shin, Young Sup Lee, Jun Young Noh, Soojin Kwak, Yoonna Jeon, Sangeun Kwon, Sunoh Jin, Young-hee Jang, Min Seong Kim, Seungtaek Song, Jong Hwan Kim, Hyoung Rae Park, Chul Min |
author_facet | Shin, Young Sup Lee, Jun Young Noh, Soojin Kwak, Yoonna Jeon, Sangeun Kwon, Sunoh Jin, Young-hee Jang, Min Seong Kim, Seungtaek Song, Jong Hwan Kim, Hyoung Rae Park, Chul Min |
author_sort | Shin, Young Sup |
collection | PubMed |
description | Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) continues to spread worldwide, with 25 million confirmed cases and 800 thousand deaths. Effective treatments to target SARS-CoV-2 are urgently needed. In the present study, we have identified a class of cyclic sulfonamide derivatives as novel SARS-CoV-2 inhibitors. Compound 13c of the synthesized compounds exhibited robust inhibitory activity (IC(50) = 0.88 μM) against SARS-CoV-2 without cytotoxicity (CC(50) > 25 μM), with a selectivity index (SI) of 30.7. In addition, compound 13c exhibited high oral bioavailability (77%) and metabolic stability with good safety profiles in hERG and cytotoxicity studies. The present study identified that cyclic sulfonamide derivatives are a promising new template for the development of anti-SARS-CoV-2 agents. |
format | Online Article Text |
id | pubmed-7640924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76409242020-11-05 Discovery of cyclic sulfonamide derivatives as potent inhibitors of SARS-CoV-2 Shin, Young Sup Lee, Jun Young Noh, Soojin Kwak, Yoonna Jeon, Sangeun Kwon, Sunoh Jin, Young-hee Jang, Min Seong Kim, Seungtaek Song, Jong Hwan Kim, Hyoung Rae Park, Chul Min Bioorg Med Chem Lett Article Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) continues to spread worldwide, with 25 million confirmed cases and 800 thousand deaths. Effective treatments to target SARS-CoV-2 are urgently needed. In the present study, we have identified a class of cyclic sulfonamide derivatives as novel SARS-CoV-2 inhibitors. Compound 13c of the synthesized compounds exhibited robust inhibitory activity (IC(50) = 0.88 μM) against SARS-CoV-2 without cytotoxicity (CC(50) > 25 μM), with a selectivity index (SI) of 30.7. In addition, compound 13c exhibited high oral bioavailability (77%) and metabolic stability with good safety profiles in hERG and cytotoxicity studies. The present study identified that cyclic sulfonamide derivatives are a promising new template for the development of anti-SARS-CoV-2 agents. Elsevier Ltd. 2021-01-01 2020-11-04 /pmc/articles/PMC7640924/ /pubmed/33160024 http://dx.doi.org/10.1016/j.bmcl.2020.127667 Text en © 2020 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Shin, Young Sup Lee, Jun Young Noh, Soojin Kwak, Yoonna Jeon, Sangeun Kwon, Sunoh Jin, Young-hee Jang, Min Seong Kim, Seungtaek Song, Jong Hwan Kim, Hyoung Rae Park, Chul Min Discovery of cyclic sulfonamide derivatives as potent inhibitors of SARS-CoV-2 |
title | Discovery of cyclic sulfonamide derivatives as potent inhibitors of SARS-CoV-2 |
title_full | Discovery of cyclic sulfonamide derivatives as potent inhibitors of SARS-CoV-2 |
title_fullStr | Discovery of cyclic sulfonamide derivatives as potent inhibitors of SARS-CoV-2 |
title_full_unstemmed | Discovery of cyclic sulfonamide derivatives as potent inhibitors of SARS-CoV-2 |
title_short | Discovery of cyclic sulfonamide derivatives as potent inhibitors of SARS-CoV-2 |
title_sort | discovery of cyclic sulfonamide derivatives as potent inhibitors of sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7640924/ https://www.ncbi.nlm.nih.gov/pubmed/33160024 http://dx.doi.org/10.1016/j.bmcl.2020.127667 |
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