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Synthesis and anti-bacterial activity of novel 1,3-phenylene-bis-N-acetyl- and N-phenylenepyrazole derivatives

机译:新型1,3-亚苯基-双-N-乙酰基和N-亚苯基吡唑衍生物的合成及抑菌活性

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The 1,1'-(5,5'-(1,3-phenylene)bis(3-aryl-4,5-dihydro-1H-pyrazole-5,1-diyl))di-ethanone ( 5a-e ) and 1,3-bis(1-phenyl-3-(aryl)-4,5-dihydro-1H-pyrazol-5-yl)benzene ( 6a-e ) were synthesized by addition of hydrazine hydrate and/or phenylhydrazine to 1,3-phenylene-bis-chalcone derivatives ( 3a-e ), respectively. The structures of obtained compounds ( 5a-e and 6a-e ) were characterized using the spectroscopic methods (NMR, IR) and elemental analysis. Addition, the in vitro antibacterial activities of compounds ( 5a-e ) was tested against the five human pathogenic bacteria. Gentamycin and Fluconazole were used as positive control. The results were given as inhibition zone (mm) and the compounds 5d and 5e showed the same activity with standard (Fluconazole) against C. albinas .
机译:1,1'-(5,5'-(1,3-亚苯基)双(3-芳基-4,5-二氢-1H-吡唑-5,1-二基))二乙酮(5a-e)通过将水合肼和/或苯肼加到1中来合成1,3-双(1-苯基-3-(芳基)-4,5-二氢-1H-吡唑-5-基)苯(6a-e) ,3-亚苯基-双查耳酮衍生物(3a-e)。使用光谱方法(NMR,IR)和元素分析来表征获得的化合物(5a-e和6a-e)的结构。另外,测试了化合物(5a-e)对五种人类病原菌的体外抗菌活性。庆大霉素和氟康唑用作阳性对照。结果以抑制区(mm)给出,化合物5d和5e显示出与标准品(氟康唑)相同的针对白念珠菌的活性。

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