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首页> 外文期刊>Organic Chemistry International >Synthesis and Characterization ofN1-Phenylhydrazine-1,2-bis(carbothioamide) and Its Evaluation for Antimicrobial, Antioxidant, and Brine Shrimp Lethality Bioassay
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Synthesis and Characterization ofN1-Phenylhydrazine-1,2-bis(carbothioamide) and Its Evaluation for Antimicrobial, Antioxidant, and Brine Shrimp Lethality Bioassay

机译:N1-苯基肼-1,2-双(碳硫酰胺)的合成,表征及其抗微生物,抗氧化和卤虾致死性生物测定的评价

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The compoundN1-phenylhydrazine-1,2-bis(carbothioamide) was synthesised from phenylisothiocyanate reacting with thiosemicarbazide refluxing the mixture in ethanol. The new compound obtained was characterised by various spectral and elemental analyses. It was subjected to antibacterial, antioxidant and brine shrimp lethality bioassay. The compound showed brine shrimp lethality with LC50value of 12.79 μg which was comparable to vincristine with LC50value of 0.33 μg. The compound did not exhibit any antimicrobial activity against Gram +ve and Gram −ve organisms, as well as against the tested fungal strains. But very good free radical scavenging activity was observed at concentration range of 0.185–100 μg with IC50values of 1.43 μg in comparison to reference standard butylated hydroxytoluene (BHT) with IC50value 16.46 μg.
机译:由苯基异硫氰酸酯与硫代氨基脲反应,将混合物在乙醇中回流,合成了化合物N1-苯基肼-1,2-双(碳硫代酰胺)。通过各种光谱和元素分析对获得的新化合物进行了表征。它经过了抗菌,抗氧化剂和盐水虾杀伤力生物测定。该化合物显示出对虾的致死性,LC50值为12.79μg,与长春新碱相当,LC50值为0.33μg。该化合物对革兰氏+ ve和革兰氏ve生物以及测试的真菌菌株均无任何抗菌活性。但是,与参考标准丁基化羟基甲苯(BHT)的IC50值为16.46μg相比,在0.185–100μg的浓度范围内观察到非常好的自由基清除活性,IC50值为1.43μg。

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