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Synthesis, antifungal and antibacterial activity of novel 1,2,4-triazole derivatives

机译:新型1,2,4-三唑衍生物的合成,抗真菌和抗菌活性

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A large number of 1,2,4-triazole-containing ring system have been incorporated into a wide variety of therapeutically interesting drug candidates including anti-inflammatory, central nervous system stimulants, antianxiety, and antimicrobial agents. To overcome the rapid development of drug resistance, new agents should preferably have chemical characteristics that clearly differ from those of existing agents. Thus led to the design and synthesize the new antimicrobial agents. A novel series of Schiff bases based on of 4-(benzylideneamino)-5-phenyl-4H-1,2,4-triazole-3-thiol scaffold was prepared by heating thiocarbohydrazide and substituted benzoic acid and subsequently, treating with substituted benzaldehydes. Seventeen derivatives were synthesized and were biologically screened for antifungal and antibacterial activity. The newly synthesized derivatives of triazole showed antifungal activity against fungal species, Microsporum gypseum; and antibacterial activity against bacterial species, Staphylococcus aureus. It was observed that none of the compounds tested showed positive results for fungi Candida albicans fungi Aspergillus niger, nor against bacterial strain Escherichia coli. Strong antifungal effects were obtained for the synthesized compounds against M. gypseum and were superior or comparable to standard drug ketoconazole. Similarly, all of the synthesized compounds exhibit strong antibacterial activity against S. aureus and were superior or comparable to standard drug streptomycin. It was found that among the triazole derivatives so synthesized, six of them, showed antifungal activity superior to ketoconazole while one of them, showed antibacterial activity superior to streptomycin. Thus, these can be the potential new molecule as an antimicrobial agent.Keywords: Antibacterial activity, antifungal activity, Microsporum gypseum, Schiff bases, Staphylococcus aureus
机译:大量的含1,2,4-三唑的环系统已被纳入多种治疗上令人感兴趣的候选药物,包括抗炎药,中枢神经系统兴奋剂,抗焦虑药和抗菌剂。为了克服耐药性的迅速发展,新药剂应优选具有明显不同于现有药剂的化学特性。从而导致设计并合成了新的抗菌剂。通过加热硫代碳酰肼和取代的苯甲酸,然后用取代的苯甲醛处理,制备了基于4-(亚苄基氨基)-5-苯基-4H-1,2,4-三唑-3-硫醇支架的新型席夫碱系列。合成了十七种衍生物,并对它们的抗真菌和抗菌活性进行了生物学筛选。新合成的三唑衍生物对真菌小孢子石膏具有抗真菌活性。和对细菌种类金黄色葡萄球菌的抗菌活性。观察到,所测试的化合物均未显示对于白色念珠菌真菌黑曲霉真菌或对细菌菌株大肠杆菌呈阳性结果。合成的化合物针对石膏支原体获得了强大的抗真菌作用,并且优于或可比标准药物酮康唑。类似地,所有合成的化合物对金黄色葡萄球菌均显示出强大的抗菌活性,并且优于或可比标准药物链霉素。发现在这样合成的三唑衍生物中,其中的六个具有优于酮康唑的抗真菌活性,而其中的一种具有优于链霉素的抗菌活性。因此,这些可能是作为抗菌剂的潜在新分子。关键词:抗菌活性,抗真菌活性,石膏小孢子菌,席夫碱,金黄色葡萄球菌

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