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首页> 外文期刊>Der Pharma Chemica: journal for medicinal chemistry, pharmaceutical chemistry and computational chemistry >Synthesis, characterization, antibacterial, antifungal evaluation of novel mannich bases of 2,5-disubstiututed indoles
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Synthesis, characterization, antibacterial, antifungal evaluation of novel mannich bases of 2,5-disubstiututed indoles

机译:2,5-二取代吲哚的新型曼尼希碱的合成,表征,抗菌,抗真菌评价

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In an effort to develop potent antimicrobial a series of mannich bases of 2,5-disubstututed indoles were prepared for investigating their antimicrobial activities. All compounds were found to be significantly active against gram positive bacteria: S. aureus, B. subtilus Gram negative bacteria: E.coli, P.aeruginosa and fungal strains: C. albicans, A. niger by tube dilution method. Compound N-((2-(4-bromophenyl)-5-nitro-1H-indol-3-yl)methyl)-Nphenyl benzenamine (MB10) and N-benzyl-N-((2-(4-bromophenyl)-5-nitro-1H-indol-3-yl) methyl) (phenyl) methanamine (MB11) emerged as the best antimicrobial agent in the present study. The structure of the synthesized compounds was confirmed by physico-chemical characteristics and spectroscopic investigations. Docking results of these two compounds with COX-2 (PDB ID: 4COX) also exhibited a strong binding profile.
机译:为了开发有效的抗菌剂,制备了一系列由2,5-二取代的吲哚组成的曼尼希碱,以研究其抗菌活性。通过试管稀释法,发现所有化合物均对革兰氏阳性菌:金黄色葡萄球菌,枯草芽孢杆菌,革兰氏阴性菌:大肠杆菌,铜绿假单胞菌和真菌菌株:白色念珠菌,黑曲霉具有显着活性。化合物N-((2-(4-溴苯基)-5-硝基-1H-吲哚-3-基)甲基)-N苯基苯甲胺(MB10)和N-苄基-N-((2-(4-溴苯基)- 5-硝基-1H-吲哚-3-基)甲基)(苯基)甲胺(MB11)成为本研究中最好的抗菌剂。通过理化特性和光谱研究证实了合成化合物的结构。这两种化合物与COX-2(PDB ID:4COX)的对接结果也显示出很强的结合特性。

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