Cargando…

Synthesis of deuterated S-217622 (Ensitrelvir) with antiviral activity against coronaviruses including SARS-CoV-2

S-217622 (Ensitrelvir) is a reversible severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) 3-chymotrypsin-like protease (3CL(pro)) inhibitor which obtained emergency regulatory approval in Japan for the treatment of SARS-CoV-2 infection on Nov 22, 2022. Herein, analogs of S-271622 with deut...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Yujian, Cao, Liu, Yan, Ming, Zhou, Jun, Yang, Sidi, Xu, Tiefeng, Huang, Siyao, Li, Kun, Zhou, Qifan, Li, Guanguan, Zhu, Yujun, Cong, Feng, Zhang, Hongmin, Guo, Deyin, Li, Yingjun, Zhang, Xumu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043954/
https://www.ncbi.nlm.nih.gov/pubmed/36997073
http://dx.doi.org/10.1016/j.antiviral.2023.105586
_version_ 1784913255408336896
author Yang, Yujian
Cao, Liu
Yan, Ming
Zhou, Jun
Yang, Sidi
Xu, Tiefeng
Huang, Siyao
Li, Kun
Zhou, Qifan
Li, Guanguan
Zhu, Yujun
Cong, Feng
Zhang, Hongmin
Guo, Deyin
Li, Yingjun
Zhang, Xumu
author_facet Yang, Yujian
Cao, Liu
Yan, Ming
Zhou, Jun
Yang, Sidi
Xu, Tiefeng
Huang, Siyao
Li, Kun
Zhou, Qifan
Li, Guanguan
Zhu, Yujun
Cong, Feng
Zhang, Hongmin
Guo, Deyin
Li, Yingjun
Zhang, Xumu
author_sort Yang, Yujian
collection PubMed
description S-217622 (Ensitrelvir) is a reversible severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) 3-chymotrypsin-like protease (3CL(pro)) inhibitor which obtained emergency regulatory approval in Japan for the treatment of SARS-CoV-2 infection on Nov 22, 2022. Herein, analogs of S-271622 with deuterium-for-hydrogen replacement were synthesized for comparison of the antiviral activities and pharmacokinetic (PK) profiles. Compared to the parent compound, C11-d2-S-217622 compound YY-278 retained in vitro activity against 3CL(pro) and SARS-CoV-2. X-ray crystal structural studies showed similar interactions of SARS-CoV-2 3CL(pro) with YY-278 and S-271622. The PK profiling revealed the relatively favorable bioavailability and plasma exposure of YY-278. In addition, YY-278, as well as S-217622, displayed broadly anti-coronaviral activities against 6 other coronaviruses that infect humans and animals. These results laid the foundation for further research on the therapeutic potential of YY-278 against COVID-19 and other coronaviral diseases.
format Online
Article
Text
id pubmed-10043954
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Published by Elsevier B.V.
record_format MEDLINE/PubMed
spelling pubmed-100439542023-03-28 Synthesis of deuterated S-217622 (Ensitrelvir) with antiviral activity against coronaviruses including SARS-CoV-2 Yang, Yujian Cao, Liu Yan, Ming Zhou, Jun Yang, Sidi Xu, Tiefeng Huang, Siyao Li, Kun Zhou, Qifan Li, Guanguan Zhu, Yujun Cong, Feng Zhang, Hongmin Guo, Deyin Li, Yingjun Zhang, Xumu Antiviral Res Article S-217622 (Ensitrelvir) is a reversible severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) 3-chymotrypsin-like protease (3CL(pro)) inhibitor which obtained emergency regulatory approval in Japan for the treatment of SARS-CoV-2 infection on Nov 22, 2022. Herein, analogs of S-271622 with deuterium-for-hydrogen replacement were synthesized for comparison of the antiviral activities and pharmacokinetic (PK) profiles. Compared to the parent compound, C11-d2-S-217622 compound YY-278 retained in vitro activity against 3CL(pro) and SARS-CoV-2. X-ray crystal structural studies showed similar interactions of SARS-CoV-2 3CL(pro) with YY-278 and S-271622. The PK profiling revealed the relatively favorable bioavailability and plasma exposure of YY-278. In addition, YY-278, as well as S-217622, displayed broadly anti-coronaviral activities against 6 other coronaviruses that infect humans and animals. These results laid the foundation for further research on the therapeutic potential of YY-278 against COVID-19 and other coronaviral diseases. Published by Elsevier B.V. 2023-05 2023-03-28 /pmc/articles/PMC10043954/ /pubmed/36997073 http://dx.doi.org/10.1016/j.antiviral.2023.105586 Text en © 2023 Published by Elsevier B.V. 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
Yang, Yujian
Cao, Liu
Yan, Ming
Zhou, Jun
Yang, Sidi
Xu, Tiefeng
Huang, Siyao
Li, Kun
Zhou, Qifan
Li, Guanguan
Zhu, Yujun
Cong, Feng
Zhang, Hongmin
Guo, Deyin
Li, Yingjun
Zhang, Xumu
Synthesis of deuterated S-217622 (Ensitrelvir) with antiviral activity against coronaviruses including SARS-CoV-2
title Synthesis of deuterated S-217622 (Ensitrelvir) with antiviral activity against coronaviruses including SARS-CoV-2
title_full Synthesis of deuterated S-217622 (Ensitrelvir) with antiviral activity against coronaviruses including SARS-CoV-2
title_fullStr Synthesis of deuterated S-217622 (Ensitrelvir) with antiviral activity against coronaviruses including SARS-CoV-2
title_full_unstemmed Synthesis of deuterated S-217622 (Ensitrelvir) with antiviral activity against coronaviruses including SARS-CoV-2
title_short Synthesis of deuterated S-217622 (Ensitrelvir) with antiviral activity against coronaviruses including SARS-CoV-2
title_sort synthesis of deuterated s-217622 (ensitrelvir) with antiviral activity against coronaviruses including sars-cov-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043954/
https://www.ncbi.nlm.nih.gov/pubmed/36997073
http://dx.doi.org/10.1016/j.antiviral.2023.105586
work_keys_str_mv AT yangyujian synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT caoliu synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT yanming synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT zhoujun synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT yangsidi synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT xutiefeng synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT huangsiyao synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT likun synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT zhouqifan synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT liguanguan synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT zhuyujun synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT congfeng synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT zhanghongmin synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT guodeyin synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT liyingjun synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2
AT zhangxumu synthesisofdeuterateds217622ensitrelvirwithantiviralactivityagainstcoronavirusesincludingsarscov2