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- W2605200212 abstract "Inhibition of mushroom tyrosinase was observed with synthetic dihydropyrano[3,2-b]chromenediones. Among them, DHPC04 displayed the most potent tyrosinase inhibitory activity with a Ki value of 4 μm, comparable to the reference standard inhibitor kojic acid. A kinetic study suggested that these synthetic heterocyclic compounds behave as competitive inhibitors for the L-DOPA binding site of the enzyme. Furthermore, molecular modeling provided important insight into the mechanism of binding interactions with the tyrosinase copper active site." @default.
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- W2605200212 date "2017-06-12" @default.
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- W2605200212 title "Inhibition of tyrosinase by 4 <i>H</i> ‐chromene analogs: Synthesis, kinetic studies, and computational analysis" @default.
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- W2605200212 doi "https://doi.org/10.1111/cbdd.13001" @default.
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