...
首页> 外文期刊>Bioorganic and medicinal chemistry >1,2,4-Triazole and 1,3,4-oxadiazole analogues: Synthesis, MO studies, in silico molecular docking studies, antimalarial as DHFR inhibitor and antimicrobial activities
【24h】

1,2,4-Triazole and 1,3,4-oxadiazole analogues: Synthesis, MO studies, in silico molecular docking studies, antimalarial as DHFR inhibitor and antimicrobial activities

机译:1,2,4-三唑和1,3,4-氧代唑类似物:合成,莫研究,硅分子对接研究,抗疟药作为DHFR抑制剂和抗菌活性

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

1,2,4-Triazole and 1,3,4-oxadiazole analogues are of interest due to their potential activity against microbial and malarial infections. In search of suitable antimicrobial and antimalarial compounds, we report here the synthesis, characterization and biological activities of 1,2,4-triazole and 1,3,4-oxadiazole analogues (SS 1-SS 10). The molecules were characterized by IR, mass, H-1 NMR, C-13 NMR and elemental analysis. The in vitro antimicrobial activity was investigated against pathogenic strains, the results were explained with the help of DFT and PM6 molecular orbital calculations. In vitro cytotoxicity and genotoxicity of the molecules were studied against S. pombe cells. In vitro antimalarial activity was studied. The active compounds were further evaluated for enzyme inhibition efficacy against the receptor Pf-DHFR computationally as well as in vitro to prove their candidature as lead dihydrofolate reductase inhibitors. (C) 2017 Elsevier Ltd. All rights reserved.
机译:由于它们对微生物和疟疾感染的潜在活性,1,2,4-三唑和1,3,4-氧代唑类似物具有感兴趣。 为了寻找合适的抗微生物和抗疟性化合物,我们在此报告1,2,4-三唑和1,3,4-氧代唑类似物(SS 1-SS 10)的合成,表征和生物活性。 该分子的特征在于IR,质量,H-1 NMR,C-13 NMR和元素分析。 研究了对致病菌菌株的体外抗微生物活性,从DFT和PM6分子轨道计算的帮助下解释了结果。 研究了分子的体外细胞毒性和遗传毒性。 研究了体外抗疟活性。 进一步评估活性化合物,用于计算上酶PF-DHFR的酶抑制效果,以及在体外作为铅二氢醇还原酶抑制剂证明其候选物。 (c)2017 Elsevier Ltd.保留所有权利。

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