Discovery of macrocyclic covalent inhibitors for severe acute respiratory syndrome coronavirus 2 3CL protease

被引:0
|
作者
Tang, Xiubo [1 ]
Hou, Kai [1 ]
Chen, Xiaowu [1 ]
Fan, Wenyuan [1 ]
Wu, Hao [1 ]
Lu, Changliang [1 ]
He, Gong-Xin [1 ]
机构
[1] Shanghai CureGene Pharmaceut Co Ltd, 2nd floor,Bldg C1,1976 middle Gaoke Rd,ZhangJiang, Shanghai 201210, Peoples R China
关键词
SARS-CoV-2; 3CL(pro); Covalent inhibition; Macrocyclization; PEPTIDE; DRUG; PEPTIDOMIMETICS;
D O I
10.1016/j.bmc.2024.117846
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The coronavirus disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been spread worldwide for more than 3 years. Although the hospitalization rate and mortality have decreased dramatically due to wide vaccination effort and improved treatment options, the disease is still a global health issue due to constant viral mutations, causing negative impact on social and economic activities. In addition, long COVID and complications arising from COVID-19 weeks after infection have become a concern for public health experts. Therefore, better treatments for COVID-19 are still needed. Herein, we describe a class of macrocyclic peptidomimetic compounds that are potent inhibitors of SARS-Cov-2 3CL protease (3CL(pro)). Significantly, some of the compounds showed a higher stability against human liver microsomes (HLM t(1/2) > 180 min) and may be suitable for oral administration without the need for a pharmacokinetic (PK) boosting agent such as ritonavir.
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页数:14
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