首页> 外文期刊>Life sciences >Network pharmacology and molecular docking reveal the mechanism of Scopoletin against non-small cell lung cancer
【24h】

Network pharmacology and molecular docking reveal the mechanism of Scopoletin against non-small cell lung cancer

机译:网络药理学和分子对接揭示了微氨基对非小细胞肺癌的机制

获取原文
获取原文并翻译 | 示例
           

摘要

Aims: Scopoletin is a natural anticarcinogenic and antiviral coumarin component. Many studies have proved its anti-cancer effect, and after the preliminary screening of this study, Scopoletin had the best inhibitory effect on Non-small cell lung cancer (NSCLC). But its mechanism for treating NSCLC is still unclear. Therefore, network pharmacology and molecular docking technology were used to explore the potential anti-NSCLC targets and pathways of Scopoletin. The results were verified in vitro.
机译:目的:东莨菪内酯是一种天然的抗癌和抗病毒香豆素成分。许多研究已经证明了其抗癌作用,在本研究的初步筛选后,东莨菪内酯对非小细胞肺癌(NSCLC)的抑制效果最好。但其治疗非小细胞肺癌的机制尚不清楚。因此,网络药理学和分子对接技术被用来探索东莨菪内酯潜在的抗NSCLC靶点和途径。结果在体外得到验证。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号