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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...

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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
Descripción
Sumario: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.