A Review on Structure-Activity Relationship of Dietary Polyphenols Inhibiting α-Amylase

The inhibitory effects of dietary polyphenols against -amylase have attracted great interest among researchers. The aim of this review is to give an overview of the research reports on the structureactivity relationship of polyphenols inhibiting -amylase. The molecular structures that influence the inhibition are the following: (1) The hydroxylation of flavonoids improved the inhibitory effect on -amylase; (2) Presence of an unsaturated 2,3-bond in conjugation with a 4-carbonyl group has been associated with stronger inhibition; (3) The glycosylation of flavonoids decreased the inhibitory effect on -amylase depending on the conjugation site and the class of sugar moiety; (4) The methylation and methoxylation of flavonoids obviously weakened the inhibitory effect; (5) The galloylated catechins have higher inhibition than nongalloylated catechins; the catechol-type catechins were stronger than the pyrogallol-type catechins; the inhibition activities of the catechins with 2,3-trans structure were higher than those of the catechins with 2,3-cis structure; (6) Cyanidin-3-glucoside showed higher inhibition against than cyanidin and cyanidin-3-galactoside and cyanidin-3,5-diglucoside had no inhibitory activity; (7) Ellagitannins with -galloyl groups at glucose C-1 positions have higher inhibitory effect than the -galloyl and nongalloyl compounds and the molecular weight of ellagitannins is not an important element.