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Investigation of the Antimycobacterial Activity of 8-hydroxyquinolines

机译:8-羟基喹啉的抗分枝杆菌活性的研究

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摘要

A series of styrylquinolines and quinolineamides based on the 8-hydroxyquinoline moiety were investigated as potential antimycobacterial agents. The lipophilicity of the compounds was measured using RP-HPLC and the tests of their activity against Mycobacterium kansasii, the M. avium complex, M. smegmatis, M. abscessus, M. tuberculosis and M. avium paratuberculosis was performed. Several of the compounds that were obtained appeared to be more effective than isoniazid and ciprofloxacin. The 5,7-dinitro-8-hydroxyquinoline derivative possessed the highest potency against M. abscessus and M. Smegmatis, which was about twice as effective as ciprofloxacin, while 2-(2-hydroxystyryl)-8-hydroxyquinoline-7-carboxylic acid appeared to be comparable with the standard drugs that are against the M. avium complex. The structure activity relationships are discussed.
机译:研究了一系列基于8-羟基喹啉部分的苯乙烯基喹啉和喹啉酰胺作为潜在的抗分枝杆菌药物。使用RP-HPLC测量化合物的亲脂性,并且测试它们对堪萨斯分枝杆菌,鸟分枝杆菌复合体,耻垢分枝杆菌,脓肿支原体,结核分枝杆菌和副结核分枝杆菌的活性。获得的几种化合物似乎比异烟肼和环丙沙星更有效。 5,7-二硝基-8-羟基喹啉衍生物对脓肿分支杆菌和耻垢分枝杆菌具有最高效力,约为环丙沙星的两倍,而2-(2-羟基苯乙烯基)-8-羟基喹啉-7-羧酸似乎与抗鸟分枝杆菌复合物的标准药物具有可比性。讨论了结构活动关系。

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