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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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作者 Miao Zheng Bo Feng +16 位作者 Yumin Zhang Xin Liu NaZhao Hui Liu Zichao Xu Xinheng He zhiyan qu ShizhaoChen Zhidong Jiang Xi Cheng Hong Liu Yi Zang Linxiang Zhao Jie Zheng Leike Zhang Jia Li Yu Zhou 《Acta Pharmaceutica Sinica B》 SCIE CAS CSCD 2024年第7期3286-3290,共5页
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 c... 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. 展开更多
关键词 Non-covalent PL^(pro)inhibitors Antiviral activity Structural-based drug design Imidazo[4 5-b]pyridine scaffold
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