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Synthesis and Antimicrobial Activity of New Imidazole-Hydrazone Derivatives

机译:新型咪唑-衍生物的合成及抑菌活性

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摘要

Hydrazones demonstrated significant antimicrobial activity, antitubercular activity and antitumoral activity in medicinal areas. The imidazole nucleus is well known to play an important role in living organisms since it is incorporated into the histidine molecule and many other important biological, pharmacological and therapeutic activities. Condensation of 4-phenyl-1H-imidazole-2-carbaIdehyde (3) with various selected benzohydrazides (4a-m) resulted in imidazole-hydrazone derivatives (5a-m). They were evaluated for antibacterial and antifungal activity against A. niger, C. albicans (fungal strains), E. coli and P. aeruginosa (Gram-negative bacteria), S. aureus and S. pyogenes (Gram-positive bacteria) using griseofluvin (for fungi) and ciprofloxacin (for bacteria) as the standard drugs. In general, it is observed that most of the compounds were found to be potent against both the bacterial and fungal strains.
机译:dra在医学领域显示出显着的抗菌活性,抗结核活性和抗肿瘤活性。众所周知,咪唑核在活生物体中起重要作用,因为它被掺入组氨酸分子和许多其他重要的生物学,药理和治疗活性中。 4-苯基-1H-咪唑-2-氨基乙醛(3)与各种选定的苯并酰肼(4a-m)缩合生成咪唑-hydr衍生物(5a-m)。使用灰黄霉素评估了它们对黑曲霉,白色念珠菌(真菌菌株),大肠杆菌和铜绿假单胞菌(革兰氏阴性细菌),金黄色葡萄球菌和化脓性链球菌(革兰氏阳性细菌)的抗菌和抗真菌活性。 (用于真菌)和环丙沙星(用于细菌)作为标准药物。通常,观察到发现大多数化合物对细菌和真菌菌株均有效。

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