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- W2610714733 abstract "Xanthine oxidase is a potential target for treatment of hyperuricemia and gout. In this study, a number of A- and B-ring carboxylated aurone derivatives were synthesized and evaluated for their ability to inhibit xanthine oxidase in vitro. According to the results obtained, two different ranges of inhibitory activity were observed. The aurones with carboxylic acid group at the 4′-position of B-ring were found to be potent inhibitors of the enzyme with IC50 values in the low micromolar range. The effects of these compounds were about 50 fold higher than of A-ring modified aurones with carboxymethoxy group at the 6-position. The binding modes of the carboxylated aurones in the active site of xanthine oxidase were explained using molecular docking calculations." @default.
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- W2610714733 date "2017-07-01" @default.
- W2610714733 modified "2023-10-17" @default.
- W2610714733 title "Carboxylated aurone derivatives as potent inhibitors of xanthine oxidase" @default.
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- W2610714733 doi "https://doi.org/10.1016/j.bmc.2017.04.048" @default.
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