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Crystal structure of SARS-CoV-2 main protease in complex with the natural product inhibitor shikonin illuminates a unique binding mode 被引量:8
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作者 Jian Lia Xuelan Zhou +10 位作者 Yan Zhang Fanglin Zhong Cheng Lin Peter J.McCormick Feng Jiang Jun Luo Huan Zhou Qisheng Wang Yang Fu Jingjing Duan Jin Zhang 《Science Bulletin》 SCIE EI CSCD 2021年第7期661-663,M0003,共4页
Almost everyone is susceptible to the severe acute respiratorysyndrome coronavirus 2(SARS-CoV-2),an RNA virus,which cancause many symptoms and even death among high-risk individu-als[1,2].The main protease(M^(Pro),als... Almost everyone is susceptible to the severe acute respiratorysyndrome coronavirus 2(SARS-CoV-2),an RNA virus,which cancause many symptoms and even death among high-risk individu-als[1,2].The main protease(M^(Pro),also known as 3CL^(Pro))is a cys-teine protease essential for producing infectious virions and thusan attractive target for drug development.Up to now,many studiesusing either in silico ligand docking or drug discovery based onavailable structures have been performed to discover new MPTO.inhibiting agents[3.4]. 展开更多
关键词 小分子抑制剂 紫草素 冠状病毒 药物研发 药物靶点 天然产物 中药活性成分 结合模式
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