期刊文献+

2-(N-丙基)-6-三氟甲氧基苯并噻唑抗肿瘤活性研究 被引量:1

Research on anti-tumour activity of 2-(N-propylamine)-6-trifluoromethoxy-benzothiazole
下载PDF
导出
摘要 目的研究2-(N-丙基)-6-三氟甲氧基苯并噻唑的抗肿瘤活性和机制。方法采用CCK-8法测定药物对HeLa、HepG2、MCF-7和SP2/0肿瘤细胞增殖的影响;Hoechst 33258染色和Annexin V-FITC/PI双染法,检测药物对MCF-7细胞的促凋亡作用,观察药物作用后肿瘤细胞的形态;采用细胞划痕实验,检测药物对肿瘤细胞迁移能力的影响。结果 2-(N-丙基)-6-三氟甲氧基苯并噻唑能明显抑制4种肿瘤细胞的增殖,且具有较好的选择性,特别是对MCF-7作用最明显,其IC_(50)值为(12.91±0.69)μmol·L^(-1)。对MCF-7细胞有比较强的抗迁移作用,划痕愈合率较对照组明显降低,还可诱导MCF-7细胞的早期凋亡。结论 2-(N-丙基)-6-三氟甲氧基苯并噻唑可抑制肿瘤细胞的增殖,并且通过诱导MCF-7细胞的早期凋亡,抑制MCF-7细胞迁移,从而发挥其增殖抑制作用。 Aim To study the anti-tumour activity and mechanism of 2-(N-propylamine)-6-trifluoromethoxy-benzothiazole. Methods The anti-proliferative activities against HeLa,HepG2,MCF-7 and SP2/0 cancer cell lines were assessed by CCK-8 assay.The morphological changes of cancer cells were observed by Hoechst staining.Effects on the cell migration were evaluated by monolayer cells wound healing assay.The cell apoptosis analysis was evaluated by using the flow cytometric analysis. Results Compound 2-(N-propylamine)-6-trifluoromethoxy-benzothiazole showed good selectivity and inhibitory effects against four tumor cell lines.Especially,the effects on MCF-7 cells were very significant.This compound could inhibit the migration of MCF-7 cells and induce early apoptosis. Conclusions 2-(N-propylamine)-6-trifluoromethoxy-benzothiazole can inhibit the proliferation of four tumor cell lines.It shows inhibitory effects on MCF-7 cells by inducing early apoptosis.
作者 张飞 刘振国 王海芳 武祥龙 刘柳 蔺旭彬 吕文君 刘浩 ZHANG Fei;LIU Zhen-guo;WANG Hai-fang;WU Xiang-long;LIU Liu;LIN Xu-bin;LYU Wen-jun;LIU Hao(Key Lab for Space Bioscience and Biotechnology,School of Life Sciences,Northwestern PolytechnicalUniversity,Xi’an710072,China;Intensive Care Unit,Shaanxi Provincial People’s Hospital,Xi’an710068,China;Shaanxi Key Lab of Integrated Traditional and Western Medicine for Prevention and Treatmentof Cardiovascular Diseases,Shaanxi University of Chinese Medicine,Xi’an712046,China)
出处 《中国药理学通报》 CAS CSCD 北大核心 2019年第5期644-648,共5页 Chinese Pharmacological Bulletin
基金 国家自然科学基金资助项目(No 21202130) 大学生创新创业训练计划项目(No 201710699335)
关键词 苯并噻唑 肿瘤 肿瘤细胞 迁移 增殖 凋亡 benzothiazole cancer tumour cells migration proliferation apoptosis
  • 相关文献

参考文献5

二级参考文献45

  • 1胡燚,郭敏飞,韦萍,陈振初.离子液体中烷基化反应研究进展[J].化学试剂,2006,28(2):79-82. 被引量:6
  • 2郭峰,朱炳阳,迟秀玲,黄红林.迷迭香酸抗过氧化氢诱导血管平滑肌细胞凋亡作用的研究[J].中国药理学通报,2007,23(3):365-370. 被引量:26
  • 3Domino E F, Unna K R, Kerwin J. Pharmacological properties of benzazoles. I. Relationship between strue-ture and paralyzing action[ J ]. J Pharmacol Exp Ther, 1952,1115(4) :486 -497.
  • 4Jimonet P, Audiau F, Barreau M, et al. Riluzole se- ries. Synthesis and in vivo "antiglutamate" activity of 6-substituted-2-benzothiazolamines and 3-substituted- 2- [ J ]. J Med Chem, 1999,42 (15) :2828 - 2843.
  • 5Joyce L L, Batey R A. Heterocycle formation via pal- ladium-catalyzed intramolecular oxidative C-H bond functionalization:An efficient strategy for the synthesis of 2-aminobenzothiazoles [ J ]. Org Lett,2009,11 ( 13 ) : 2792 - 2795.
  • 6Saha P, Ramana T, Purkait N, et 02. Ligand-free cop- per-catalyzed synthesis of substituted benzimidazoles, 2-aminobenzimidazoles,2-aminobenzothiazoles, and ben- zoxazoles [ J]. J Org Chem,2009,74(13) :8719 - 8725.
  • 7Falb E, Sterling J, Herzig Y, et al. Propargyl-triflu- ommethoxy-aminobenzothiazole derivatives, their prep- aration and use : US 20 130 172 364 [ P]. 2013.
  • 8Sheldriek G M. SHELXL-97, program for crystal strut- tare refinement [ K ]. Germany: University of Gettingen, 1997.
  • 9Sheldrick G M. SHELXL-97,program for crystal struc- tare solution [ K ]. Germany:University of Gottingen, 1997.
  • 10刘华业,张晓飞,高文涛.3-乙酰基-2-氯吲哚中氨基的烷基化和苄基化保护研究[J].化学试剂,2010,32(9):832-834. 被引量:3

共引文献23

同被引文献1

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部