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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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