首页> 外文期刊>chemistryselect >Design, Docking, and Synthesis of Quinoline-2H-1,2,4-triazol-3(4H)-ones as Potent Anticancer and Antitubercular Agents
【24h】

Design, Docking, and Synthesis of Quinoline-2H-1,2,4-triazol-3(4H)-ones as Potent Anticancer and Antitubercular Agents

机译:Design, Docking, and Synthesis of Quinoline-2H-1,2,4-triazol-3(4H)-ones as Potent Anticancer and Antitubercular Agents

获取原文
获取原文并翻译 | 示例
           

摘要

abstract_textpA new series quinoline-2H-1,2,4-triazol-3(4H)-ones 7 g-n and 11 g-n were designed and synthesized. Docking studies of title compounds with DNA (PDB: 1AU5) and with long-chain enoyl-acyl carrier protein reductase (InhA) enzyme (PDB ID: 4TZK) as anticancer and antitubercular targets showed good insights on the possible interactions. Further, the compounds were tested for in vitro anticancer activity against HeLa human cervix tumor cell line and also in vitro antitubercular activity against M. tuberculosis H37Rv MTB (ATCC-27294). Some of the compounds exhibited promising activities in both the protocols. Hence, these compounds may be considered as pharmacological lead molecules of interest./p/abstract_text

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