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New 5-Hydroxy-2-(hydroxymethyl)-4H-pyran-4-one Derivative Has Both Tyrosinase Inhibitory and Antioxidant Properties

机译:新的5-羟基-2-(羟甲基)-4H-吡喃-4-酮衍生物兼具酪氨酸酶抑制作用和抗氧化作用

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摘要

Kojic acid,5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one,is produced from carbohydrate sources in an aerobic process by a variety of microorganisms.It showed broad biological activities such as inhibition of tyrosinase,scavenging of the free radicals,chelating activity of metal ions4 and prevention of photodamage.Its various activities are due to gamma-pyranone structure having enolic hydroxy 1 group.Recently,enolic hydroxyl group of kojic acid has been focused as an alternative of carboxylic acid in retinoid structure.We synthesized 3,4-methylenedioxy cinnamic acid ester of kojic acid as a new retinoidal compound.In this study,we evaluated biological activities of new kojic acid derivative 1,2-((3E)-4(2H,3H-benzo[3,4-d]l,3-dioxolan-5-yl)-2-oxo-but-3-enyloxy)-5-hydroxy-4H-pyran-4-one.
机译:5-羟-2-(羟甲基)-4H-吡喃-4-酮曲酸是由多种微生物在需氧过程中从碳水化合物来源产生的,具有广泛的生物学活性,如抑制酪氨酸酶,清除酪氨酸等。自由基,金属离子的螯合活性和防止光损伤。其各种活性是由于具有烯醇式羟基1的γ-吡喃酮结构引起的。我们合成了曲酸的3,4-亚甲基二氧基肉桂酸酯作为一种新的类维生素A化合物。在这项研究中,我们评估了新曲酸衍生物1,2-((3E)-4(2H,3H-苯并[3] ,4-d] l,3-二氧戊环-5-基)-2-氧代-丁-3-烯氧基)-5-羟基-4H-吡喃-4-酮。

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