The 3C-like protease (3CLpro) is an essential enzyme for the replication of SARS-CoV-2 and other coronaviruses and thus is a target for coronavirus drug discovery. Nearly all inhibitors of coronavirus 3CLpro reported so far are covalent inhibitors. Here, we report the development of specific, noncovalent inhibitors of 3CLpro. The most potent one, WU-04, effectively blocks SARS-CoV-2 replications in human cells with EC(50) values in the 10-nM range. WU-04 also inhibits the 3CLpro of SARS-CoV and MERS-CoV with high potency, indicating that it is a pan-inhibitor of coronavirus 3CLpro. WU-04 showed anti-SARS-CoV-2 activity similar to that of PF-07321332 (Nirmatrelvir) in K18-hACE2 mice when the same dose was administered orally. Thus, WU-04 is a promising drug candidate for coronavirus treatment.
Development of Highly Potent Noncovalent Inhibitors of SARS-CoV-2 3CLpro.
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作者:Hou Ningke, Shuai Lei, Zhang Lijing, Xie Xuping, Tang Kaiming, Zhu Yunkai, Yu Yin, Zhang Wenyi, Tan Qiaozhu, Zhong Gongxun, Wen Zhiyuan, Wang Chong, He Xijun, Huo Hong, Gao Haishan, Xu You, Xue Jing, Peng Chen, Zou Jing, Schindewolf Craig, Menachery Vineet, Su Wenji, Yuan Youlang, Shen Zuyuan, Zhang Rong, Yuan Shuofeng, Yu Hongtao, Shi Pei-Yong, Bu Zhigao, Huang Jing, Hu Qi
| 期刊: | ACS Central Science | 影响因子: | 10.400 |
| 时间: | 2023 | 起止号: | 2023 Jan 25; 9(2):217-227 |
| doi: | 10.1021/acscentsci.2c01359 | ||
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