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Triprenylated flavonoids from Dorstenia psilurus and their alpha-glucosidase inhibition properties
Turibio K Tabopda1, Joseph Ngoupayo, Patrice K Awoussong
1Organic Chemistry Department, University of Yaoundé I, P.O. Box 8664, Yaoundé, Cameroon. ttabopda@yahoo.fr
Abstract:
Six new unusual C-4'-prenylated flavonols, dorsilurins F-K (1-6), together with six known compounds were isolated from the roots of Dorstenia psilurus, and their structures were elucidated on the basis of spectroscopic evidence. The isolated compounds exhibited moderate to low alpha-glucosidase inhibitory activity. Dorsilurin F (1), with three unmodified prenyl groups, was the most active, while dorsilurin K (6), with only one unmodified prenyl group, was the least active compound. Furthermore, NMR data of dorsilurin C (7), isolated some years ago from the same plant, have been revised.
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