Article(id=1319291275476578563, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291166823142311, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2026.09.036, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1792473151320, onlineDateStr=2026-10-20, pubDate=1788969600000, pubDateStr=2026-09-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1792473151320, onlineIssueDateStr=2026-10-20, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1792473151320, creator=13701087609, updateTime=1792473151320, updator=13701087609, issue=Issue{id=1319291166823142311, tenantId=1146029695717560320, journalId=1255847919539208197, year='2026', volume='44', issue='9', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1788969600000', pubDateStr='2026-09-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=1, specialIssue=null, createTime=1792473125414, creator='13701087609', updateTime=1792473357559, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1319292140618896016, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291166823142311, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1319292140618896017, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291166823142311, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=202, endPage=205, ext={EN=ArticleExt(id=1319291275669516548, articleId=1319291275476578563, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Study on Anti-SARS-CoV-2 Mechanism of Emodin and Prediction of Antiviral Activity of Anthraquinone Compounds, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective To study the inhibitory effect of emodin on SARS-CoV-2 RNA polymerase (RdRp) and main protease (Mpro) and predict the anti-SARS-CoV-2 activity of anthraquinone compounds.
Methods A cell-level SARS-CoV-2 RNA polymerase catalytic reaction system was used to detect the inhibitory activity of emodin against RdRp. An in vitro fluorescence polarization model was used to test the inhibitory activity of emodin against SARS-CoV-2 Mpro. Molecular docking technology was used to study the binding mode of anthraquinone compounds at the active site of RdRp.
Results The experiment showed that emodin inhibited RdRp with inhibition rates of 42.01%±3.43%, 47.28%±11.20% and 84.28%±4.34% at concentrations of 10, 25, 50 μmol/L, respectively. It did not show significant inhibitory activity against Mpro at drug concentrations of 25, 50, 100 μmol/L. Anthraquinone compounds can occupy the NTPs channel of the target enzyme, thereby hindering the entry of substrate molecules.
Conclusion This experiment confirmed that emodin has a significant inhibitory effect on SARS-CoV-2 RNA polymerase. The small molecule anthraquinone compounds in this paper should have strong anti-SARS-CoV-2 activity.
, authors=Jingfang LIU
1, Qian LIU
2, Yingnan ZHAO
3, Lei YANG
3, Yujia WANG
4, Jianyuan ZHAO
4, Yanlei SU
3, Dianxing SUN
3, Shan CEN
4, authorsList=Jingfang LIU, Qian LIU, Yingnan ZHAO, Lei YANG, Yujia WANG, Jianyuan ZHAO, Yanlei SU, Dianxing SUN, Shan CEN, authorCompany=null, correspAuthors=Yanlei SU, Shan CEN, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1319291275996672261, articleId=1319291275476578563, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=大黄素抗新型冠状病毒机制研究及蒽醌类化合物抗病毒活性预测, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的 研究大黄素对新型冠状病毒RNA聚合酶、主蛋白酶的抑制作用,并预测蒽醌类化合物抗新型冠状病毒活性。
方法 利用细胞水平的新型冠状病毒RNA聚合酶催化反应体系检测大黄素对靶酶的抑制活性;利用体外荧光偏振模型测试大黄素对于新型冠状病毒主蛋白酶的抑制活性;应用分子对接技术研究蒽醌类化合物在RNA聚合酶活性位点处的结合方式。
结果 实验显示,大黄素在10、25、50 μmol/L浓度对RNA聚合酶抑制率分别为42.01%±3.43%、47.28%±11.20%、84.28%±4.34%;在25、50、100 μmol/L药物浓度并未表现出对主蛋白酶的显著抑制活性;蒽醌类化合物可占据靶酶NTPs通道从而阻碍底物分子的进入。
结论 实验证实大黄素对新型冠状病毒RNA聚合酶具有明显的抑制作用;小分子蒽醌类化合物应具有较强的抗新型冠状病毒活性。
, authors=刘京芳
1, 刘倩
2, 赵英男
3, 杨雷
3, 王宇佳
4, 赵建元
4, 苏彦雷
3, 孙殿兴
3, 岑山
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刘京芳(1979-),女,河北石家庄人,副主任医师,硕士,研究方向:中医临床及方剂。
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