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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
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.
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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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