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- W2014747912 abstract "Typical heterocyclic compounds substituted with various functional groups found in Maillard reaction were examined for antioxidant activity. Pyrroles exhibited the greatest antioxidant activity among all heterocyclic compounds tested. All pyrroles inhibited hexanal oxidation by almost 100% at a concentration of 50 μg/ml over 40 days. Addition of a formyl group to the pyrrole ring enhanced antioxidative activity remarkably. Pyrrole-2-carboxaldehyde inhibited hexanal oxidation by about 90% at 5 μg/ml. Unsubstituted furan exhibited the greatest antioxidant activity among furans tested. Addition of all functional groups tested to the furan decreased antioxidative activity. Antioxidant activity of thiophene was increased by the addition of methyl groups, but addition of formyl groups to thiophene decreased antioxidant activity. Thiazoles and pyrazines were ineffective antioxidants at all concentrations tested." @default.
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- W2014747912 date "2002-11-01" @default.
- W2014747912 modified "2023-10-03" @default.
- W2014747912 title "Antioxidative activity of heterocyclic compounds formed in Maillard reaction products" @default.
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- W2014747912 doi "https://doi.org/10.1016/s0531-5131(02)01007-5" @default.
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