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- W2156685597 abstract "The catalytic promiscuity of the novel benzophenone C-glycosyltransferase, MiCGT, which is involved in the biosynthesis of mangiferin from Mangifera indica, was explored. MiCGT exhibited a robust capability to regio- and stereospecific C-glycosylation of 35 structurally diverse druglike scaffolds and simple phenolics with UDP-glucose, and also formed O- and N-glycosides. Moreover, MiCGT was able to generate C-xylosides with UDP-xylose. The OGT-reversibility of MiCGT was also exploited to generate C-glucosides with simple sugar donor. Three aryl-C-glycosides exhibited potent SGLT2 inhibitory activities with IC50 values of 2.6×, 7.6×, and 7.6×10(-7) M, respectively. These findings demonstrate for the first time the significant potential of an enzymatic approach to diversification through C-glycosidation of bioactive natural and unnatural products in drug discovery." @default.
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- W2156685597 date "2015-09-01" @default.
- W2156685597 modified "2023-09-24" @default.
- W2156685597 title "Probing the Catalytic Promiscuity of a Regio- and Stereospecific C-Glycosyltransferase from<i>Mangifera indica</i>" @default.
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- W2156685597 doi "https://doi.org/10.1002/anie.201506505" @default.
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