Synthesis, antimicrobial activity and cytotoxicity of some new carbazole derivatives
作者:Zafer Asim Kaplancikli、Leyla Yurttaş、Gülhan Turan-Zitouni、Ahmet Özdemir、Rasime Özic、Şafak Ulusoylar-Yıldırım
DOI:10.3109/14756366.2011.622273
日期:2012.12.1
work, some N-(9-Ethyl-9H-carbazole-3-yl)-2-(phenoxy)acetamide derivatives were synthesised and evaluated for their antimicrobial activity and cytotoxicity. The structural elucidation of the compounds was performed by IR, (1)H-NMR, (13)C-NMR and FAB(+)-MS spectral data and elemental analyses. The title compounds were obtained by reacting 2-chloro-N-(9-ethyl-9H-carbazole-3-yl)acetamide with some substituted
在这项工作中,合成了一些N-(9-乙基-9H-咔唑-3-基)-2-(苯氧基)乙酰胺衍生物,并对其抗微生物活性和细胞毒性进行了评估。通过IR,(1)H-NMR,(13)C-NMR和FAB(+)-MS光谱数据和元素分析进行化合物的结构阐明。通过使2-氯-N-(9-乙基-9H-咔唑-3-基)乙酰胺与一些取代的酚反应获得标题化合物。研究了合成的化合物对微球菌,枯草芽孢杆菌,铜绿假单胞菌,金黄色葡萄球菌,大肠埃希菌,单核细胞增生李斯特菌和白色念珠菌的抗菌和抗真菌活性。化合物N-(9-乙基-9H-咔唑-3-基)-2-(4-乙基苯氧基)乙酰胺(2c)和N-(9-乙基-9H-咔唑-3-基)-2-(喹啉) -8-酰氧基)乙酰胺(2n)表现出显着的抗菌活性。还使用MTT测定法研究了这些化合物的细胞毒性作用,并且发现2n对NIH / 3T3细胞具有最低的细胞毒性活性。