Cargando…

Discovery of novel bicyclic[3.3.0]proline peptidyl α-ketoamides as potent 3CL-protease inhibitors for SARS-CoV-2

The outbreak of SARS-CoV-2 has caused global crisis on health and economics. The multiple drug-drug interaction risk associated with ritonavir warrants specialized assessment before using Paxlovid. Here we report a multiple-round SAR study to provide a novel bicyclic[3.3.0]proline peptidyl α-ketoami...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Xiaoxin, Li, Peng, Huang, Jianzhou, Yang, Yaxun, Zhang, Haoyu, Wang, Zheng, Zhu, Zhenzhen, Wang, Jingjing, Zhang, Jianchen, Chen, Kevin, He, Haiying, Long, Chaofeng, Chen, Shuhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176891/
https://www.ncbi.nlm.nih.gov/pubmed/37182612
http://dx.doi.org/10.1016/j.bmcl.2023.129324
_version_ 1785040515747545088
author Chen, Xiaoxin
Li, Peng
Huang, Jianzhou
Yang, Yaxun
Zhang, Haoyu
Wang, Zheng
Zhu, Zhenzhen
Wang, Jingjing
Zhang, Jianchen
Chen, Kevin
He, Haiying
Long, Chaofeng
Chen, Shuhui
author_facet Chen, Xiaoxin
Li, Peng
Huang, Jianzhou
Yang, Yaxun
Zhang, Haoyu
Wang, Zheng
Zhu, Zhenzhen
Wang, Jingjing
Zhang, Jianchen
Chen, Kevin
He, Haiying
Long, Chaofeng
Chen, Shuhui
author_sort Chen, Xiaoxin
collection PubMed
description The outbreak of SARS-CoV-2 has caused global crisis on health and economics. The multiple drug-drug interaction risk associated with ritonavir warrants specialized assessment before using Paxlovid. Here we report a multiple-round SAR study to provide a novel bicyclic[3.3.0]proline peptidyl α-ketoamide compound 4a, which is endowed with excellent antiviral activities and pharmacokinetic properties. Also, in vivo HCoV-OC43 neonatal mice model demonstrated compound 4a has good in vivo efficacy. Based on these properties, compound 4a worth further SAR optimization with the goal to develop compounds with better pharmacokinetic properties and finally to realize single agent efficacy in human.
format Online
Article
Text
id pubmed-10176891
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Published by Elsevier Ltd.
record_format MEDLINE/PubMed
spelling pubmed-101768912023-05-12 Discovery of novel bicyclic[3.3.0]proline peptidyl α-ketoamides as potent 3CL-protease inhibitors for SARS-CoV-2 Chen, Xiaoxin Li, Peng Huang, Jianzhou Yang, Yaxun Zhang, Haoyu Wang, Zheng Zhu, Zhenzhen Wang, Jingjing Zhang, Jianchen Chen, Kevin He, Haiying Long, Chaofeng Chen, Shuhui Bioorg Med Chem Lett Article The outbreak of SARS-CoV-2 has caused global crisis on health and economics. The multiple drug-drug interaction risk associated with ritonavir warrants specialized assessment before using Paxlovid. Here we report a multiple-round SAR study to provide a novel bicyclic[3.3.0]proline peptidyl α-ketoamide compound 4a, which is endowed with excellent antiviral activities and pharmacokinetic properties. Also, in vivo HCoV-OC43 neonatal mice model demonstrated compound 4a has good in vivo efficacy. Based on these properties, compound 4a worth further SAR optimization with the goal to develop compounds with better pharmacokinetic properties and finally to realize single agent efficacy in human. Published by Elsevier Ltd. 2023-06-15 2023-05-12 /pmc/articles/PMC10176891/ /pubmed/37182612 http://dx.doi.org/10.1016/j.bmcl.2023.129324 Text en © 2023 Published by Elsevier Ltd. 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
Chen, Xiaoxin
Li, Peng
Huang, Jianzhou
Yang, Yaxun
Zhang, Haoyu
Wang, Zheng
Zhu, Zhenzhen
Wang, Jingjing
Zhang, Jianchen
Chen, Kevin
He, Haiying
Long, Chaofeng
Chen, Shuhui
Discovery of novel bicyclic[3.3.0]proline peptidyl α-ketoamides as potent 3CL-protease inhibitors for SARS-CoV-2
title Discovery of novel bicyclic[3.3.0]proline peptidyl α-ketoamides as potent 3CL-protease inhibitors for SARS-CoV-2
title_full Discovery of novel bicyclic[3.3.0]proline peptidyl α-ketoamides as potent 3CL-protease inhibitors for SARS-CoV-2
title_fullStr Discovery of novel bicyclic[3.3.0]proline peptidyl α-ketoamides as potent 3CL-protease inhibitors for SARS-CoV-2
title_full_unstemmed Discovery of novel bicyclic[3.3.0]proline peptidyl α-ketoamides as potent 3CL-protease inhibitors for SARS-CoV-2
title_short Discovery of novel bicyclic[3.3.0]proline peptidyl α-ketoamides as potent 3CL-protease inhibitors for SARS-CoV-2
title_sort discovery of novel bicyclic[3.3.0]proline peptidyl α-ketoamides as potent 3cl-protease inhibitors for sars-cov-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176891/
https://www.ncbi.nlm.nih.gov/pubmed/37182612
http://dx.doi.org/10.1016/j.bmcl.2023.129324
work_keys_str_mv AT chenxiaoxin discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT lipeng discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT huangjianzhou discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT yangyaxun discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT zhanghaoyu discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT wangzheng discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT zhuzhenzhen discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT wangjingjing discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT zhangjianchen discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT chenkevin discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT hehaiying discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT longchaofeng discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2
AT chenshuhui discoveryofnovelbicyclic330prolinepeptidylaketoamidesaspotent3clproteaseinhibitorsforsarscov2