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...
Autores principales: | , , , , , , , , , , , , |
---|---|
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 |