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Hydroxyphenyl thiosemicarbazones as inhibitors of mushroom tyrosinase and antibrowning agents

机译:羟苯硫半脲酮类作为蘑菇酪氨酸酶抑制剂和抗褐变剂

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摘要

Tyrosinase is a metalloenzyme involved in o-hydroxylation of monophenols and oxidation of o-diphenols to o-quinones, with formation of brown or black pigments (melanines). Tyrosinase inhibitors are of great interest in medicine and cosmetics (skin whitening compounds), but also in food and beverage industry (antibrowning agents). Here we report on the activity as mushroom tyrosinase inhibitors of a series of hydroxyphenyl thiosemicarbazones (1-5): one of them revealed an inhibitory activity stronger than kojic acid, used as reference. Enzymatic inhibition activity was confirmed by colorimetric measurements on small wheels of Fuji apples treated with the hydroxyphenyl thiosemicarbazones. The mechanism of action of compounds 1-5 was investigated by molecular modelling and by studying in solution their speciation with Cu(II) ions, the ions in the active site of the enzyme. Finally, compounds 1-5 were tested on human fibroblasts: they are not cytotoxic and they do not activate cells in a pro-inflammatory way.
机译:酪氨酸酶是一种金属酶,参与单酚的邻羟基化和邻二酚氧化为邻醌,形成棕色或黑色颜料(三聚氰胺)。酪氨酸酶抑制剂在医学和化妆品(皮肤增白化合物)中非常重要,在食品和饮料行业(抗褐变剂)中也很重要。在这里,我们报道了一系列羟苯基硫代半氨基甲酮类化合物(1-5)作为蘑菇酪氨酸酶抑制剂的活性:其中一个显示出比曲酸更强的抑制活性,用作参考。通过比色法在用羟苯基硫代半缩氨基脲处理的富士苹果的小轮上进行比色测量证实了酶抑制活性。通过分子模型研究了化合物1-5的作用机理,并在溶液中研究了它们与Cu(II)离子的形态,即酶活性位点中的离子。最后,化合物1-5在人成纤维细胞上进行了测试:它们没有细胞毒性,并且不以促炎性方式激活细胞。

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