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首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Synthesis, Characterization, Antibacterial and Urease Inhibition Studies of Some Novel Symmetrical N~3,N~3-bis-(disubstituted)isophthalyl-bis-(thioureas)
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Synthesis, Characterization, Antibacterial and Urease Inhibition Studies of Some Novel Symmetrical N~3,N~3-bis-(disubstituted)isophthalyl-bis-(thioureas)

机译:新型对称的N〜3,N〜3-双(二取代)间苯二甲酰双(硫脲)的合成,表征,抗菌和脲酶抑制研究

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摘要

A series of some novel N~3,N~3-bis-(disubstituted)isophmalyl-bis-(thioureas), with general formula [C6H4{CONHCSNR1R2}2], where R1 = H (4a-4d, 4f, 4g, 4i, 4j), C6H5(4e)( C6H_(11)(4h) and R2 = C5H4N~3(4a), 4-C6H4COOH(4b), 3-No2C6H4(4c), 2-No2C6H4(4d), C6H5(4e), 2,4(CH3)2C6H3(4f), C6H_(11)(4g, 4h), C5H4N(4i), 3-NH2C6H4(4j) have been synthesized in good to excellent yields by reaction of isophthaloyl isotbiocyanate with primary and secondary amines using dry acetone as solvent. These compounds 3a-j have been characterized by elemental analyses, infrared and ~1H NMR spectroscopy. These compounds were screened for their antibacterial activity against bacterial species, Bacillus subtilis, Staphylococcus aureus, Escherichia coli, S. sonii, Salmonella typhi and Pseudomonas aeroginosa. Some compounds showed potent activity against some bacterial strains and others exhibited strong antibacterial activity. The synthesized compounds 4a-j were also evaluated for urease inhibition and found to exhibit varying degree of urease inhibition activity. Compounds 4a-d were found to be the most active, exhibiting IC_(50)= 26.3 ± 0.5 to 31.1 ± 0.3 μM. It was concluded that these compounds may be a potential source of active antibacterial agents and some of these compounds also exhibit promising urease inhibitory activity.
机译:一系列新颖的N〜3,N〜3-双-(双取代)异麦二烷基-双-(硫脲),通式为[C6H4 {CONHCSNR1R2} 2],其中R1 = H(4a-4d,4f,4g, 4i,4j),C6H5(4e)(C6H_(11)(4h)和R2 = C5H4N〜3(4a),4-C6H4COOH(4b),3-No2C6H4(4c),2-No2C6H4(4d),C6H5( 4e),2,4(CH3)2C6H3(4f),C6H_(11)(4g,4h),C5H4N(4i),3-NH2C6H4(4j)已通过异邻苯二甲酰基异异氰酸酯与伯反应生成了良好的产率化合物3a-j已通过元素分析,红外和〜1H NMR光谱进行了表征,并筛选了这些化合物对细菌,枯草芽孢杆菌,金黄色葡萄球菌,大肠杆菌,S的抗菌活性。这些化合物对某些细菌菌株具有有效的活性,而其他化合物则具有很强的抗菌活性,还对合成的化合物4a-j进行了脲酶抑制作用的评估并发现了不同程度的脲酶抑制活性。发现化合物4a-d是最具活性的,表现出IC_(50)= 26.3±0.5至31.1±0.3μM。结论是这些化合物可能是活性抗菌剂的潜在来源,其中一些化合物还显示出有希望的脲酶抑制活性。

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