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噻吩取代长链查尔酮对肿瘤侵袭的抑制作用

赵松峰 张珩 魏涵 刘芝梅 张晓坚 刘子维

中国药理学通报2018,Vol.34Issue(4):467-472,6.
中国药理学通报2018,Vol.34Issue(4):467-472,6.DOI:10.3969/j.issn.1001-1978.2018.04.007

噻吩取代长链查尔酮对肿瘤侵袭的抑制作用

Tumor invasion inhibition of thiophene substituted long chain chalcones

赵松峰 1张珩 2魏涵 1刘芝梅 3张晓坚 1刘子维2

作者信息

  • 1. 郑州大学第一附属医院药学部,河南 郑州 450052
  • 2. 武汉工程大学化工与制药学院,湖北 武汉 430205
  • 3. 人福医药集团光谷生物城园区科福新药公司,湖北 武汉 430074
  • 折叠

摘要

Abstract

Aim To elucidate the structure-activity re-lationship between a new class of long chain chalcone compounds and tumor invasion. Methods The basic idea of the research was to enhance the specificity by prolonging the molecular structure. Based on the lead compound TSAHC, the thiophene was used as the main derivative at the carbonyl groups to obtain six new chalcones. Then we evaluated the anti-tumor activities of the compounds and the expression of key protein MMP-2 of the tumor invasion. Finally, six new com-pounds were docked to the protein by the SYBYL soft-ware. Results The structures of the six compounds were confirmed by H-NMR and MS. Among them, compound 2,3 showed fine capability to inhibit tumor invasion. The docking results also showed that the sul-fonamide and thiophene groups of the compounds had positive contribution to the target binding of the com-pounds. Conclusion Cell experiments and molecular docking show that the long chain modification of chal-cone by using thiophene as a derivative group can sig-nificantly enhance the anti-tumor invasion.

关键词

查尔酮/肿瘤侵袭/MMP-2/分子对接/构效关系/噻吩

Key words

chalcone/tumor invasion/MMP-2/mo-lecular docking/QSAR/thiophene

分类

医药卫生

引用本文复制引用

赵松峰,张珩,魏涵,刘芝梅,张晓坚,刘子维..噻吩取代长链查尔酮对肿瘤侵袭的抑制作用[J].中国药理学通报,2018,34(4):467-472,6.

基金项目

国家自然科学基金资助项目(No 31700291) (No 31700291)

湖北省自然科学基金面上项目(No 2017CFB712) (No 2017CFB712)

郑州大学第一附属医院院内创新青年基金项目(No ZDYQNNJJ-2015) (No ZDYQNNJJ-2015)

武汉工程大学青年人才项目(No 237114) (No 237114)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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