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棕矢车菊素对新型冠状病毒RNA聚合酶的抑制活性

邸琨 刘琪 吴巧娜 刘晶磊 王宇佳 苏彦雷 孙殿兴 赵建元

药学研究2026,Vol.45Issue(2):130-133,149,5.
药学研究2026,Vol.45Issue(2):130-133,149,5.DOI:10.13506/j.cnki.jpr.2026.02.002

棕矢车菊素对新型冠状病毒RNA聚合酶的抑制活性

Inhibitory activity of jaceosidin on the SARS-CoV-2 RNA polymerase

邸琨 1刘琪 2吴巧娜 1刘晶磊 2王宇佳 3苏彦雷 2孙殿兴 2赵建元3

作者信息

  • 1. 石家庄市第三医院,河北 石家庄 050011
  • 2. 联勤保障部队第九八○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
  • 折叠

摘要

Abstract

Objective To explore the inhibitory activity of the flavonoid jaceosidin against the RNA polymerase of the novel coronavirus.Methods Molecular docking was first employed to investigate the binding mode of jaceosidin at the active site of RNA polymerase,to determine whether jaceosidin could stably bind to the NTPs channel and obstruct the entry of substrates.Subsequently,the inhibitory pharmacological activity of jaceosidin against RNA polymerase was evaluated using a cell-based assay system for the catalytic reaction of the novel coronavirus RNA polymerase.Results Jaceosidin exhibited favorable binding to the active site of RNA polymerase,occupying the NTPs channel and hindering the entry of nucleotides,thereby achieving pharmacological action to inhibit RNA polymerase-mediated nucleic acid replication.The results of pharmacological experiments at the cellular level demonstrated that jaceosidin possesses inhibitory activity against RNA polymerase,albeit with weaker activity compared to remdesivir.However,jaceosidin exhibited lower cytotoxicity compared to remdesivir.Conclusion The findings of this study indicate that jaceosidin exhibits inhibitory activity against RNA polymerase,providing a potential reference for the development of anti-novel coronavirus drugs.

关键词

新型冠状病毒/RNA聚合酶/活性位点/棕矢车菊素/分子对接/活性测试

Key words

SARS-CoV-2/RNA polymerase/Active site/Jaceosidin/Molecular dock/Activity test

分类

医药卫生

引用本文复制引用

邸琨,刘琪,吴巧娜,刘晶磊,王宇佳,苏彦雷,孙殿兴,赵建元..棕矢车菊素对新型冠状病毒RNA聚合酶的抑制活性[J].药学研究,2026,45(2):130-133,149,5.

基金项目

河北省医学科研课题项目(No.20241370) (No.20241370)

药学研究

2095-5375

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