首页> 外文期刊>中国化学:英文版 >Design, Synthesis and Cu2+ Recognition of β-Diketoacid and Quinoxalone Derivatives Bearing Caffeoyl or Galloyl Moieties Linked by Arylamide as Potential HIV Integrase Inhibitors
【24h】

Design, Synthesis and Cu2+ Recognition of β-Diketoacid and Quinoxalone Derivatives Bearing Caffeoyl or Galloyl Moieties Linked by Arylamide as Potential HIV Integrase Inhibitors

机译:β-二酮酸和喹诺酮衍生物与咖啡酰胺或没食子酰基部分的合成,设计和Cu2 +的识别与芳酰胺连接作为潜在的HIV整合酶抑制剂

获取原文
获取原文并翻译 | 示例
           

著录项

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