Abstract
Two new xanthones, 1,8-dihydroxy-3-methoxyxanthone
7-O-[α-L-rhamnopyranosyl(1 → 2)-β-D-glucopyranoside]
(1) and 1,8- dihydroxy-3-methoxyxanthone
7-O-[α-L-rhamnopyranosyl(1 → 3)-α-L-rhamno-pyranosyl
(1 → 2)-β-D-xylopyranoside] (2), together with 26 known
xanthones (3–28), were isolated from the aqueous ethanol
extract of the traditional Chinese herb Swertia mussotii. Their
structures were elucidated via spectroscopic analyses including 2D NMR. The
inhibition of α-glucosidase by the isolated xanthones was evaluated
by an in vitro high-throughput screening assay. Our results indicated
that 1,3,5,8-tetrahydroxyxanthone is the best inhibitor with an
IC50 value of 5.33 ± 0.09 µM, while the O-glycosylated
xanthones were poor α-glycosidase inhibitors.
Key words
Gentianaceae -
Swertia mussotii
- xanthones -
α-glucosidase inhibitor - diabetes mellitus