首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Syntheses and evaluation of 3-(3-bromo phenyl)-5-phenyl-1-(thiazolo (4,5-b) quinoxaline-2-yl)-2-pyrazoline derivatives.
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Syntheses and evaluation of 3-(3-bromo phenyl)-5-phenyl-1-(thiazolo (4,5-b) quinoxaline-2-yl)-2-pyrazoline derivatives.

机译:3-(3-溴苯基)-5-苯基-1-(噻唑(4,5-b)喹喔啉-2-基)-2-吡唑啉衍生物的合成和评价。

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摘要

A variety of 3-(3-bromo phenyl)-5-phenyl-1-(thiazolo [4,5-b] quinoxaline-2-yl)-2-pyrazoline were obtained by the refluxing of 1-N-thiocarbamoyl 3,5-diphenyl-2-pyrazoline with 2,3-dichloroquinoxaline. The chemical structures of the compounds were elucidated by UV, IR, (1)H NMR, and (13)C NMR spectroscopy. The purity of the compounds was confirmed by their elemental analysis. The antiamoebic activity of these compounds was evaluated by microdilution method against HMI:IMSS strain of Entamoeba histolytica and the IC(50) values were compared with the standard drug metronidazole. Some of the quinoxaline derivatives showed less IC(50) values than metronidazole. To elucidate the toxic effect, MTT assay was performed using kidney epithelial cell line. The results showed that all the compounds are non-toxic.
机译:通过1-N-硫代氨基甲酰基3的回流,获得了各种3-(3-溴苯基)-5-苯基-1-(噻唑并[4,5-b]喹喔啉-2-基)-2-吡唑啉, 5-二苯基-2-吡唑啉与2,3-二氯喹喔啉。通过UV,IR,(1)H NMR和(13)C NMR光谱阐明了化合物的化学结构。化合物的纯度通过其元素分析确认。通过微稀释法评估了这些化合物对溶血性变形杆菌的HMI:IMSS菌株的抗厌氧活性,并将IC(50)值与标准药物甲硝唑进行了比较。某些喹喔啉衍生物的IC(50)值低于甲硝唑。为了阐明毒性作用,使用肾上皮细胞系进行了MTT测定。结果表明所有化合物均无毒。

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