Department of Studies in Chemistry, University of Mysore, Manasagangotri, Mysore 570 006, India.
Eur J Med Chem. 2010 Jun;45(6):2677-82. doi: 10.1016/j.ejmech.2010.02.021. Epub 2010 Feb 12.
In the present investigation, a series of novel {5-chloro-2-[(3-(substitutedphenyl)-1,2,4-oxadiazol-5-yl)-methoxy]-phenyl}-(phenyl)-methanones (3a-i) have been synthesized from 5-(chloromethyl)-3-substitutedphenyl-1,2,4-oxadiazole (2a-i). The newly synthesized compounds were characterized by IR, NMR (1H and 13C), mass spectral and elemental analysis. The title compounds were investigated for in-vitro qualitative (zone of inhibition) and quantitative (MIC) antibacterial activity by agar cup plate and microtitration methods, respectively. The minimum inhibitory concentration and structure activity relationships (SARs) were evaluated. Amongst the synthesized compounds in this series, {5-chloro-2-[(3-(2,5-difluoro-4-methyl-phenyl)-1,2,4-oxadiazol-5-yl)-methoxy]-phenyl}-(phenyl)-methanone (3d) was found to exhibit significant activity with MICs of 21.5, 22.4, 29.8 and 30.6 microg/mL against Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Klebsiella pneumoniae, respectively.
在本研究中,我们合成了一系列新型的{5-氯-2-[(3-(取代苯基)-1,2,4-恶二唑-5-基)-甲氧基]-苯基}-(苯基)-甲酮(3a-i),其原料为 5-(氯甲基)-3-取代苯基-1,2,4-恶二唑(2a-i)。新合成的化合物通过红外光谱、核磁共振氢谱(1H 和 13C)、质谱和元素分析进行了表征。采用琼脂杯碟法和微量稀释法对标题化合物进行了体外定性(抑菌圈)和定量(MIC)抗菌活性测试。评估了最小抑菌浓度和构效关系(SARs)。在所合成的化合物中,{5-氯-2-[(3-(2,5-二氟-4-甲基-苯基)-1,2,4-恶二唑-5-基)-甲氧基]-苯基}-(苯基)-甲酮(3d)对枯草芽孢杆菌、金黄色葡萄球菌、大肠杆菌和肺炎克雷伯菌的 MIC 值分别为 21.5、22.4、29.8 和 30.6 μg/mL,显示出显著的活性。