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Tyrosinase Inhibition and Mutagenicity of Phenolic Compounds from Mulbeny Leaves

机译:酪氨酸酶抑制作用和穆尔班尼叶中酚类化合物的致突变性

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The tyrosinase inhibition activity and mutagenicity as assessed by the Ames test on phenolic antioxidants (5-Caffeoyl quinic acid, 3,4-Dihydroxy cinnamic acid, Quercetin 3-O-p-D-glucopyranose, Kaempferol 3-Op-D-glucopyranose) and the ethyl acetate fraction isolated from mulbeny leaves were examined. The ethyl acetate fraction and chlorogenic acid exhibited weaker tyrosinase inhibitory activities than kojic acid. In addition, the ethyl acetate fraction from mulbeny leaves, containing phenolic antioxidants, showed no mutagenicity by the Ames test
机译:通过Ames试验评估酚类抗氧化剂(5-咖啡酰奎尼酸,3,4-二羟基肉桂酸,槲皮素3-OpD-吡喃葡萄糖,山奈酚3-Op-D-吡喃葡萄糖)和酪氨酸酶对酪氨酸酶的抑制活性和诱变性。检查了从桑树叶子分离的级分。乙酸乙酯级分和绿原酸显示出比曲酸弱的酪氨酸酶抑制活性。此外,通过Ames试验,来自桑树叶的乙酸乙酯级分含有酚类抗氧化剂,没有显示出致突变性。

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