Abstract
Bioactivity-guided fractionation methods were used to identify and purify active components in Tinta Cão grape pomace extract (GPE) that inhibit intestinal α-glucosidases. One active α-glucosidase inhibitor and one new natural product determined as 6-O-(p-coumaroyl)-D-glucopyranoside and methyl 6-O-(p-coumaroyl)-β-D-galactopyranoside, respectively, were isolated from GPE that were previously shown to potently inhibit α-glucosidase. Analysis of the relationship between structures and activity suggested that C(1)-OH of saccharide moiety in phenolic glycosides is necessary for this potent inhibition of intestinal α-glucosidases for the potential development of a novel anti-hyperglycaemic dietary supplement.