应用化学 ›› 2016, Vol. 33 ›› Issue (9): 1067-1072.DOI: 10.11944/j.issn.1000-0518.2016.09.150420

• 研究论文 • 上一篇    下一篇

新型1,1-二氧代-4H-苯并[1,2,4]-噻二嗪类衍生物的合成及其抗肿瘤活性

谭绪霞a,李世宁a,赵杰b,毛伸a,毛龙飞a,徐桂清a*()   

  1. a河南师范大学化学化工学院 河南 新乡 453007
    b天方药业有限公司 河南 驻马店 463000
  • 收稿日期:2015-11-30 接受日期:2016-03-24 出版日期:2016-08-23 发布日期:2016-08-23
  • 通讯作者: 徐桂清
  • 基金资助:
    国家自然科学基金(21402043);河南省产学研项目(132107000035)

Synthesis and Antitumor Activity of Novel 4H-1,2,4-Benzothiadiazine 1,1-Dioxide Derivatives

TAN Xuxiaa,LI Shininga,ZHAO Jieb,MAO Shena,MAO Longfeia,XU Guiqinga*()   

  1. aSchool of Chemistry and Chemical Engineering,He'nan Normal university,Xinxiang,He'nan 453007,China
    bTopfond Pharmaceutical Limited by Share Ltd,Zhumadian,He'nan 463000,China
  • Received:2015-11-30 Accepted:2016-03-24 Published:2016-08-23 Online:2016-08-23
  • Contact: XU Guiqing
  • Supported by:
    Supported by the National Natural Science Foundation of China(No.21402043), the Industry, University, Research Project of He'nan(No.132107000035)

摘要:

以2-硝基苯磺酰氯为起始原料,经多步反应合成了12种新型1,1-二氧代-4H-苯并[1,2,4]-噻二嗪类衍生物,产物收率高,水溶性好,并经1H NMR、13C NMR、MS-ESI和元素分析法确证结构。 用MTT法测试了这类衍生物对肝癌细胞HepG-2生长的抑制作用,结果显示目标化合物能不同程度地抑制肿瘤细胞生长,其中7-氨甲基-3-环丙基-1,1-二氧代-4H-苯并[1,2,4]-噻二嗪 (7c)对肝癌细胞HepG-2的抗性显著,最高抑制率达到79.3%。

关键词: 二氧代-4H-苯并[1,2,4]-噻二嗪类衍生物, 合成, 抗肿瘤活性

Abstract:

Twelve unreported 4H-1,2,4-benzothiadiazine 1,1-dioxide derivatives were synthesized from 2-nitrobenzene sulfonyl chloride with good water-solubility in high yields. These compounds were characterized by 1H NMR, 13C NMR, MS-ESI and elemental analysis. Their inhibiting effects on HepG-2 cell were evaluated with MTT protocol. The results show that 7-(aminomethyl)-3-cyclopropyl-1,1-dioxide-4H-benzo[e][1,2,4]thiadiazine(7c) exhibits the highest inhibition rate of 79.3% among the synthesized compounds.

Key words: 4H-benzothiadiazine dioxides derivatives, synthesis, antitumor activities