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首页> 外文期刊>Turkish journal of chemistry >Synthesis and in Vitro Antimicrobial and Cytotoxicity Activities of 2-[(2-nitro-l-phenylalkyl)thio]benzoic Acid Derivatives
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Synthesis and in Vitro Antimicrobial and Cytotoxicity Activities of 2-[(2-nitro-l-phenylalkyl)thio]benzoic Acid Derivatives

机译:2 - [(2-硝基-L-苯基烷基)硫酸衍生物的合成和体外抗微生物和细胞毒性活性

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In this research 14 compounds were tested for their antimicrobial activity.The synthesis of 7 compounds corresponding to 2-[(2-nitro-l-phenyl-propyl)thio]benzoic acids 4 has not been reported before and 7 compounds corresponding to 2-[(2-nitro-l-phenyl-ethyl)thio]benzoic acid 3 were reported by our research group.The antibacterial activity of the title compounds was evaluated by 2 Gram (+) (Staphylococcus aureus,Bacillus subtilis) and 2 Gram (-)(Pseudomonas aeruginosa,Escherichia coli) microorganisms.The antifungal activity of the compounds was also determined against yeast-like fungi (Candida albicans,C.krusei).For antibacterial activity,ampicillin and for antifungal activity,fluconazole and ketoconazole have been used as reference compounds.All of the 2-[(2-nitro-l-phenyl-ethyl)thio]benzoic acid 3 derivatives were more active than the reference compound ketoconazole in the antifungal activity test.The title compounds were also screened by consecutive dilution to explore their toxicity to a Vero cell line.Except for 3d and 3e all of the compounds 3 exhibited lower toxicity than ketoconazole.
机译:在该研究中,测试了14种化合物,用于它们的抗微生物活性。对应于2 - [(2-硝基-1-苯基 - 丙基)硫代]苯甲酸4的7种化合物的合成尚未报道,并且对应于2-的7种化合物[(2-硝基-1-苯基 - 乙基)硫代]苯甲酸3被我们的研究组报道。标题化合物的抗菌活性由2克(+)(葡萄球菌,枯草芽孢杆菌,枯草芽孢杆菌)和2克( - )(假单胞菌铜绿假单胞菌,大肠杆菌)微生物。还针对酵母状真菌(Candida albicans,C.krusei)测定化合物的抗真菌活性。对于抗菌活性,氨苄青霉素和用于抗真菌活性,已经使用氟康唑和酮康唑作为参考化合物,其中2 - [(2-硝基-1-苯基 - 乙基)硫代]苯甲酸3衍生物比抗真菌活性试验中的参考化合物酮康唑更活跃。还通过连续稀释筛选标题化合物探索他们的毒性y到Vero细胞系。3D和3e所有化合物3表现出比酮康唑的低毒性。

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