Article(id=1319291618847469857, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291472856338924, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2026.07.013, 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=1792473233186, onlineDateStr=2026-10-20, pubDate=1783612800000, pubDateStr=2026-07-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1792473233186, onlineIssueDateStr=2026-10-20, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1792473233186, creator=13701087609, updateTime=1792473233186, updator=13701087609, issue=Issue{id=1319291472856338924, tenantId=1146029695717560320, journalId=1255847919539208197, year='2026', volume='44', issue='7', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1783612800000', pubDateStr='2026-07-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1792473198379, creator='13701087609', updateTime=1792473406504, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1319292345858773669, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291472856338924, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1319292345858773670, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291472856338924, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=65, endPage=67, ext={EN=ArticleExt(id=1319291620445499682, articleId=1319291618847469857, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Study on Inhibitory Pharmacological Activity of Psoralen against SARS-CoV-2 Main Protease and RNA Polymerase, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective

To explore the inhibitory activity of psoralen against SARS-CoV-2 main protease (Mpro) and RNA polymerase (RdRp).

Methods

Crystal structures of Mpro and RdRp were obtained. Molecular docking technology was employed to study the interaction mode of psoralen with the active sites of both enzymes. The inhibitory activity of psoralen against Mpro was tested using an in vitro fluorescence polarization model, while the inhibitory activity against RdRp was tested using a cell-level SARS-CoV-2 RNA polymerase catalytic reaction system.

Results

Psoralen could enter the active sites of Mpro and RdRp and interact with surrounding amino acids, with the binding process releasing free energy of-5.8 kcal/mol and-7.8 kcal/mol, respectively. In the Mpro fluorescence polarization model test, psoralen showed no inhibitory activity against the target enzyme at concentrations of 50, 100 and 200 μmol/L. In the RdRp inhibition test, psoralen showed inhibition rates of 7.36%±4.26%, 16.82%±6.04% and 46.07%±9.01% at concentrations of 10, 25 and 50 μmol/L, respectively.

Conclusion

The small molecule psoralen has no inhibitory activity against Mpro, but has certain inhibitory activity against RdRp.

, authors=Pengfei HAN1, Yanlei SU2, Dianxing SUN2, Jing ZHANG3, Qian LIU4, authorsList=Pengfei HAN, Yanlei SU, Dianxing SUN, Jing ZHANG, Qian LIU, authorCompany=null, correspAuthors=Yanlei SU, Jing ZHANG, 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=1319291620806209827, articleId=1319291618847469857, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=补骨脂素对新型冠状病毒主蛋白酶及RNA聚合酶抑制药理活性的研究, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的

探索补骨脂素对新型冠状病毒主蛋白酶、RNA聚合酶的抑制活性。

方法

获取主蛋白酶、RNA聚合酶的晶体结构,运用分子对接技术研究补骨脂素与二者活性位点处的相互作用模式;利用体外主蛋白酶的荧光偏振模型、细胞水平的新型冠状病毒RNA聚合酶催化反应体系分别测试补骨脂素对主蛋白酶、RNA聚合酶的抑制活性。

结果

补骨脂素可进入主蛋白酶、RNA聚合酶的活性位点处并与周围氨基酸发生相互作用,结合过程释放自由能分别为-5.8、-7.8 kcal/mol。在Mpro荧光偏振模型测试实验中补骨脂素在50、100、200 μmol/L浓度均未表现出对靶酶的抑制活性;在抑制RNA聚合酶活性的测试实验中,补骨脂素在10、25、50 μmol/L浓度显示出对靶酶抑制率为7.36%±4.26%、16.82%±6.04%、46.07%±9.01%。

结论

小分子补骨脂素对Mpro无抑制活性,对RdRp有一定的抑制活性。

, authors=韩鹏飞1, 苏彦雷2, 孙殿兴2, 张晶3, 刘倩4, authorsList=韩鹏飞, 苏彦雷, 孙殿兴, 张晶, 刘倩, authorCompany=null, correspAuthors=苏彦雷, 张晶, authorNote=

韩鹏飞(1987-),男,河北邢台人,主管药师,学士,研究方向:中药临床药学及活性成分。

, correspAuthorsNote=
苏彦雷(1983-),男,河北石家庄人,副主任药师,硕士研究生导师,硕士,研究方向:中药活性成分研究及临床药学(呼吸专业)。E-mail:。
张晶(1981-),女,河北石家庄人,高级研究员,硕士研究生导师,博士,研究方向:微生物与生化药学。E-mail:。
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韩鹏飞(1987-),男,河北邢台人,主管药师,学士,研究方向:中药临床药学及活性成分。

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韩鹏飞(1987-),男,河北邢台人,主管药师,学士,研究方向:中药临床药学及活性成分。

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补骨脂素对新型冠状病毒主蛋白酶及RNA聚合酶抑制药理活性的研究
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韩鹏飞 1 , 苏彦雷 2 , 孙殿兴 2 , 张晶 3 , 刘倩 4
中华中医药学刊 | 国家项目点击 2026,44(7): 65-67
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中华中医药学刊 |国家项目点击 2026 , 44 (7) : 65 -67
补骨脂素对新型冠状病毒主蛋白酶及RNA聚合酶抑制药理活性的研究
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韩鹏飞1, 苏彦雷2 , 孙殿兴2, 张晶3 , 刘倩4
作者信息
  • 1.河北省眼科医院,河北 邢台 054000
  • 2.联勤保障部队第九八〇医院,河北 石家庄 050082
  • 3.中国医学科学院,北京协和医学院医药生物技术研究所,北京 100050
  • 4.河北省优抚医院,河北 石家庄 050051
通讯作者:
苏彦雷(1983-),男,河北石家庄人,副主任药师,硕士研究生导师,硕士,研究方向:中药活性成分研究及临床药学(呼吸专业)。E-mail:。
张晶(1981-),女,河北石家庄人,高级研究员,硕士研究生导师,博士,研究方向:微生物与生化药学。E-mail:。
作者简介:

韩鹏飞(1987-),男,河北邢台人,主管药师,学士,研究方向:中药临床药学及活性成分。

Study on Inhibitory Pharmacological Activity of Psoralen against SARS-CoV-2 Main Protease and RNA Polymerase
Pengfei HAN1, Yanlei SU2 , Dianxing SUN2, Jing ZHANG3 , Qian LIU4
Affiliations
  • 1.Hebei Eye Hospital, Xingtai 054001, Hebei, China
  • 2.The 980th Hospital of the Joint Logistics Support Force of the Chinese People's Liberation Army, Shijiazhuang 050082, Hebei, China
  • 3.Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
  • 4.Youfu Hospital of Hebei Province, Shijiazhuang 050051, Hebei, China
出版时间: 2026-07-10 doi: 10.13193/j.issn.1673-7717.2026.07.013
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目的

探索补骨脂素对新型冠状病毒主蛋白酶、RNA聚合酶的抑制活性。

方法

获取主蛋白酶、RNA聚合酶的晶体结构,运用分子对接技术研究补骨脂素与二者活性位点处的相互作用模式;利用体外主蛋白酶的荧光偏振模型、细胞水平的新型冠状病毒RNA聚合酶催化反应体系分别测试补骨脂素对主蛋白酶、RNA聚合酶的抑制活性。

结果

补骨脂素可进入主蛋白酶、RNA聚合酶的活性位点处并与周围氨基酸发生相互作用,结合过程释放自由能分别为-5.8、-7.8 kcal/mol。在Mpro荧光偏振模型测试实验中补骨脂素在50、100、200 μmol/L浓度均未表现出对靶酶的抑制活性;在抑制RNA聚合酶活性的测试实验中,补骨脂素在10、25、50 μmol/L浓度显示出对靶酶抑制率为7.36%±4.26%、16.82%±6.04%、46.07%±9.01%。

结论

小分子补骨脂素对Mpro无抑制活性,对RdRp有一定的抑制活性。

新型冠状病毒  /  主蛋白酶  /  RNA聚合酶  /  补骨脂素  /  分子对接  /  活性测试
Objective

To explore the inhibitory activity of psoralen against SARS-CoV-2 main protease (Mpro) and RNA polymerase (RdRp).

Methods

Crystal structures of Mpro and RdRp were obtained. Molecular docking technology was employed to study the interaction mode of psoralen with the active sites of both enzymes. The inhibitory activity of psoralen against Mpro was tested using an in vitro fluorescence polarization model, while the inhibitory activity against RdRp was tested using a cell-level SARS-CoV-2 RNA polymerase catalytic reaction system.

Results

Psoralen could enter the active sites of Mpro and RdRp and interact with surrounding amino acids, with the binding process releasing free energy of-5.8 kcal/mol and-7.8 kcal/mol, respectively. In the Mpro fluorescence polarization model test, psoralen showed no inhibitory activity against the target enzyme at concentrations of 50, 100 and 200 μmol/L. In the RdRp inhibition test, psoralen showed inhibition rates of 7.36%±4.26%, 16.82%±6.04% and 46.07%±9.01% at concentrations of 10, 25 and 50 μmol/L, respectively.

Conclusion

The small molecule psoralen has no inhibitory activity against Mpro, but has certain inhibitory activity against RdRp.

SARS-CoV-2  /  main protease  /  RNA polymerase  /  psoralen  /  molecular docking  /  activity test
韩鹏飞, 苏彦雷, 孙殿兴, 张晶, 刘倩. 补骨脂素对新型冠状病毒主蛋白酶及RNA聚合酶抑制药理活性的研究. 中华中医药学刊, 2026 , 44 (7) : 65 -67 . DOI: 10.13193/j.issn.1673-7717.2026.07.013
Pengfei HAN, Yanlei SU, Dianxing SUN, Jing ZHANG, Qian LIU. Study on Inhibitory Pharmacological Activity of Psoralen against SARS-CoV-2 Main Protease and RNA Polymerase[J]. Chinese Archives of Traditional Chinese Medicine, 2026 , 44 (7) : 65 -67 . DOI: 10.13193/j.issn.1673-7717.2026.07.013
  • 国家自然科学基金项目(81672041)
  • 河北省卫生健康委员会重点科研攻关计划项目(20241370)
  • 河北省中医药管理局科研计划项目(2024256)
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2026年第44卷第7期
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doi: 10.13193/j.issn.1673-7717.2026.07.013
  • 首发时间:2026-10-20
  • 出版时间:2026-07-10
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基金
国家自然科学基金项目(81672041)
河北省卫生健康委员会重点科研攻关计划项目(20241370)
河北省中医药管理局科研计划项目(2024256)
作者信息
    1.河北省眼科医院,河北 邢台 054000
    2.联勤保障部队第九八〇医院,河北 石家庄 050082
    3.中国医学科学院,北京协和医学院医药生物技术研究所,北京 100050
    4.河北省优抚医院,河北 石家庄 050051

通讯作者:

苏彦雷(1983-),男,河北石家庄人,副主任药师,硕士研究生导师,硕士,研究方向:中药活性成分研究及临床药学(呼吸专业)。E-mail:。
张晶(1981-),女,河北石家庄人,高级研究员,硕士研究生导师,博士,研究方向:微生物与生化药学。E-mail:。
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2种不同金属材料的力学参数
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鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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