首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >1,2,5-Oxadiazole N-oxide derivatives as potential anti-cancer agents: synthesis and biological evaluation. Part IV.
【24h】

1,2,5-Oxadiazole N-oxide derivatives as potential anti-cancer agents: synthesis and biological evaluation. Part IV.

机译:1,2,5-恶二唑N-氧化物衍生物作为潜在的抗癌药:合成和生物学评估。第四部分

获取原文
获取原文并翻译 | 示例
           

摘要

Several new 1,2,5-oxadiazole N-oxide derivatives and some deoxygenated analogues were synthesized to be tested as potential selective hypoxic cell cytotoxins. Compounds prepared were designed in order to gain insight into the mechanism of action of this kind of cytotoxin. Compounds were tested in oxia and hypoxia and they proved to be non-selective. 3-Cyano-N(2)-oxide-4-phenyl-1,2,5-oxadiazole showed the best cytotoxic activity in oxia. The cytotoxicity observed for these derivatives could be explained in terms of the electronic characteristics of the 1,2,5-oxadiazole substituents. Electrochemical and ESR studies were performed on the more cytotoxic derivative.
机译:合成了几种新的1,2,5-恶二唑N-氧化物衍生物和一些脱氧类似物,作为潜在的选择性缺氧细胞毒素进行了测试。设计制备的化合物是为了深入了解这种细胞毒素的作用机理。在缺氧和缺氧状态下对化合物进行了测试,证明它们是非选择性的。 3-氰基-N(2)-氧化物-4-苯基-1,2,5-恶二唑显示出最佳的细胞毒性活性。对于这些衍生物观察到的细胞毒性可以用1,2,5-恶二唑取代基的电子特性来解释。对细胞毒性更高的衍生物进行了电化学和ESR研究。

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