首页> 外文期刊>Molecules >Synthesis, Biological Evaluation and Structure-Activity Relationships of New Quinoxaline Derivatives as Anti-Plasmodium falciparum Agents
【24h】

Synthesis, Biological Evaluation and Structure-Activity Relationships of New Quinoxaline Derivatives as Anti-Plasmodium falciparum Agents

机译:新型喹喔啉衍生物作为抗恶性疟原虫药物的合成,生物学评价和构效关系

获取原文
           

摘要

We report the synthesis and antimalarial activities of eighteen quinoxaline and quinoxaline 1,4-di-N-oxide derivatives, eight of which are completely novel. Compounds 1a and 2a were the most active against Plasmodium falciparum strains. Structure-activity relationships demonstrated the importance of an enone moiety linked to the quinoxaline ring.
机译:我们报告了十八种喹喔啉和喹喔啉1,4-二-N-氧化物衍生物的合成和抗疟疾活性,其中八种是完全新颖的。化合物1a和2a对恶性疟原虫菌株最具活性。构效关系证明了与喹喔啉环连接的烯酮部分的重要性。

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