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首页> 外文期刊>Natural product communications >DNA Topoisomerase I Inhibitory Activity of Quinochalcone C-glycosides from the Florets of Carthamus tinctorius
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DNA Topoisomerase I Inhibitory Activity of Quinochalcone C-glycosides from the Florets of Carthamus tinctorius

机译:DNA Topoisomerase酶I抑制喹啉酮C-糖苷的抑制活性来自Carthamus Tinctorius的小花

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摘要

The DNA topoisomerase (Topo) I inhibitory activity of six quinochalcone C-glycosides (QCGs) isolated from the florets of Carthamus tinctorius were evaluated in vitro. Among them, anhydrosafflor yellow B (AHSYB, 4) and carthorquinoside B (6) could inhibit DNA Topo I at concentrations as low as 100 mu M. Molecular docking study revealed that both of them have the capacity to stabilize Topo I-DNA cleavage complex in silico interacting with the essential binding sites, such as Arg364, Thr718 and TGP11. Besides, both compounds 4 and 6 exhibited no antitumor activity by in vitro cytotoxicity assays.
机译:在体外评估从迦太基菌群小花中分离的六种喹啉C-糖苷(QCG)的DNA拓扑异构酶(TOPO)I抑制活性。 其中,Anhydrosafflor黄B(Ahsyb,4)和迦乙酮苷B(6)可以抑制低至100μm的浓度低至100μm的DNA Topo I.分子对接研究表明,它们都具有稳定Topo I-DNA切割复合物的能力 在硅中与基本结合位点相互作用,例如Arg364,Thr718和TGP11。 此外,两种化合物4和6通过体外细胞毒性测定没有表现出抗肿瘤活性。

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  • 来源
    《Natural product communications》 |2017年第11期|共2页
  • 作者单位

    Nanjing Univ Chinese Med Jiangsu Collaborat Innovat Ctr Chinese Med Resour Nanjing 210023 Jiangsu Peoples R China;

    Nanjing Univ Chinese Med Jiangsu Collaborat Innovat Ctr Chinese Med Resour Nanjing 210023 Jiangsu Peoples R China;

    Nanjing Univ Chinese Med Jiangsu Collaborat Innovat Ctr Chinese Med Resour Nanjing 210023 Jiangsu Peoples R China;

    Nanjing Univ Chinese Med Jiangsu Collaborat Innovat Ctr Chinese Med Resour Nanjing 210023 Jiangsu Peoples R China;

    Nanjing Univ Chinese Med Jiangsu Collaborat Innovat Ctr Chinese Med Resour Nanjing 210023 Jiangsu Peoples R China;

    Ocean Univ China Sch Med &

    Pharm Minist Educ China Key Lab Marine Drugs Qingdao 266003 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 自然科学总论;
  • 关键词

    Quinochalcone C-glycosides; Topoisomerase I; Molecular docking; Cytotoxicity;

    机译:喹啉酮C-糖苷;拓扑异构酶I;分子对接;细胞毒性;

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