...
首页> 外文期刊>In vivo. >Synthesis and cytotoxic activity of certain 2,3,4,9-tetrahydrofuro (2,3-b) quinolin-3,4-dione and ethyl 2-(substituted aniline) -4-oxo-4,5-dihydrofuran-3-carboxylate derivatives in murine leukemia WEHI-3 cells.
【24h】

Synthesis and cytotoxic activity of certain 2,3,4,9-tetrahydrofuro (2,3-b) quinolin-3,4-dione and ethyl 2-(substituted aniline) -4-oxo-4,5-dihydrofuran-3-carboxylate derivatives in murine leukemia WEHI-3 cells.

机译:某些2,3,4,9-四氢呋喃(2,3-b)喹啉-3,4-二酮和乙基2-(取代的苯胺)-4-氧代-4,5-二氢呋喃-3-基的合成及细胞毒性鼠白血病WEHI-3细胞中的羧酸盐衍生物。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

A series of 2,3,4,9-tetrahydrofuro[2,3-b]quinolin-3,4-dione and ethyl 2-(substituted aniline) -4-oxo-4,5-dihydrofuran-3-carboxylate were synthesized and evaluated for cytotoxicity on murine leukemia WEHI-3 cells. The cytotoxic effects of most compounds tested were dose-dependent and the structure-activity relationships indicated that N-substituted benzyl derivatives displayed a stronger inhibitory activity against murine leukemia WEHI-3 cells compared to non-N-substituted benzyl substituted derivatives.
机译:合成了一系列2,3,4,9-四氢呋喃[2,3-b]喹啉-3,4-二酮和2-(取代苯胺)-4-氧代-4,5-二氢呋喃-3-羧酸乙酯并评估了其对鼠白血病WEHI-3细胞的细胞毒性。测试的大多数化合物的细胞毒性作用是剂量依赖性的,并且结构-活性关系表明,与非N-取代的苄基取代的衍生物相比,N-取代的苄基衍生物显示出对鼠白血病WEHI-3细胞更强的抑制活性。

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