Division of Agricultural Chemicals, IARI, Pusa Campus, New Delhi 110 012, India.
Eur J Med Chem. 2011 Sep;46(9):4089-99. doi: 10.1016/j.ejmech.2011.06.009. Epub 2011 Jun 23.
Novel nalidixic acid based 1,2,4-triazole derivatives were synthesized and characterized using spectral techniques like (1)H NMR, (13)C NMR, IR and mass spectrometry. All these compounds were screened for antimicrobial activity against five bacteria and two pathogenic fungi. Most of these compounds showed better antimicrobial activity than the parent compound, 4-amino-5-mercapto-1,2,4-triazole. Among all the screened compounds, 3-{6-(2-chlorophenyl)-1,2,4-triazolo [3,4-b] [1,3,4]thiadiazol-3-yl}-1-ethyl-7-methyl-1,8-naphthyridin-4(1H)-one (23) was emerged as promising antimicrobial agent (MIC = 16 μg/mL). Quantitative structure activity relationship (QSAR) analysis was carried out using various distance-based topological indices, steric and hydrophobic parameters. Based on the QSAR analysis it is indicative that lipophilic and steric parameters are the pre-requisites for these molecules to act as potent antimicrobial agents.
新型基于萘啶酸的 1,2,4-三唑衍生物通过(1)H NMR、(13)C NMR、IR 和质谱等光谱技术进行合成和表征。所有这些化合物都针对五种细菌和两种致病性真菌进行了抗菌活性筛选。与母体化合物 4-氨基-5-巯基-1,2,4-三唑相比,大多数这些化合物显示出更好的抗菌活性。在所筛选的化合物中,3-{6-(2-氯苯基)-1,2,4-三唑并[3,4-b][1,3,4]噻二唑-3-基}-1-乙基-7-甲基-1,8-萘啶-4(1H)-酮(23)表现出作为有前途的抗菌剂(MIC = 16 μg/mL)。使用各种基于距离的拓扑指数、立体和疏水性参数进行了定量构效关系(QSAR)分析。基于 QSAR 分析表明,亲脂性和立体参数是这些分子作为有效抗菌剂的前提条件。