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- W2415706035 endingPage "10139" @default.
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- W2415706035 abstract "Although numerous biologically active molecules exist as glycosides in nature, information on the activity, stability, and solubility of glycosylated antioxidants is rather limited to date. In this work, a wide variety of antioxidants were glycosylated using different phosphorylase enzymes. The resulting antioxidant library, containing α/β-glucosides, different regioisomers, cellobiosides, and cellotriosides, was then characterized. Glycosylation was found to significantly increase the solubility and stability of all evaluated compounds. Despite decreased radical-scavenging abilities, most glycosides were identified to be potent antioxidants, outperforming the commonly used 2,6-bis(1,1-dimethylethyl)-4-methylphenol (BHT). Moreover, the point of attachment, the anomeric configuration, and the glycosidic chain length were found to influence the properties of these phenolic glycosides." @default.
- W2415706035 created "2016-06-24" @default.
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- W2415706035 date "2015-11-11" @default.
- W2415706035 modified "2023-10-17" @default.
- W2415706035 title "Enzymatic Glycosylation of Phenolic Antioxidants: Phosphorylase-Mediated Synthesis and Characterization" @default.
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- W2415706035 doi "https://doi.org/10.1021/acs.jafc.5b04380" @default.
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