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Discovery and characterization of novel potent non-covalent small molecule inhibitors targeting papain-like protease from SARS-CoV-2

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摘要 To the Editor:The papain-like protease(PL^(pro)),as one of the most important proteases of SARS-CoV-2,has emerged as a highly promising target protein,its inhibitor probably holds dual potentials,namely blocking the cleavage of viral polyprotein and intercepting the deubiquitination and deISGylation functions to restore antiviral immunity1.
出处 《Acta Pharmaceutica Sinica B》 SCIE CAS CSCD 2024年第7期3286-3290,共5页 药学学报(英文版)
基金 National Natural Science Foundation of China(82151219,82130105) the Strategic Priority Research Program of Chinese Academy of Sciences(SIMM010109,SIMM010111) Shanghai Institute of Materia Medica of Chinese Academy of Sciences(SIMM0120231003)for the financial support.
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  • 1Yi Zang,Mingbo Su,Qingxing Wang,Xi Cheng,Wenru Zhang,Yao Zhao,Tong Chen,Yingyan Jiang,Qiang Shen,Juan Du,Qiuxiang Tan,Peipei Wang,Lixin Gao,Zhenming Jin,Mengmeng Zhang,Cong Li,Ya Zhu,Bo Feng,Bixi Tang,Han Xie,Ming-Wei Wang,Mingyue Zheng,Xiaoyan Pan,Haitao Yang,Yechun Xu,Beili Wu,Leike Zhang,Zihe Rao,Xiuna Yang,Hualiang Jiang,Gengfu Xiao,Qiang Zhao,Jia Li.High-throughput screening of SARS-CoV-2 main and papain-like protease inhibitors[J].Protein & Cell,2023,14(1):17-27. 被引量:2

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