α-Glucosidase Inhibitors from the Stems of Knema globularia

Abstract

Six new compounds, globunones A-F (1-6), and two new flavonoids (7 and 8) together with nine known compounds (9-17) were isolated from the stems of Knema globularia. The chemical structures of 1-8 were elucidated by an analysis of their NMR and high-resolution electrospray ionization mass spectrometry data as well as by comparison with literature values. The absolute configurations were determined using time-dependent density functional theory electronic circular dichroism (TD-DFT-ECD). Globunones A-E (1-5) represent the initial combined structures of a flavan-3-ol core and a 1,4-benzoquinone core. Globunone F (6) is the first flavanone-type compound bearing a 2-(2,4-dihydroxyphenyl)-2-oxoethyl group found to date in Nature. Compounds 1-3 and 6-17 were tested for their yeast α-glucosidase inhibitory activity. All compounds tested (except for 13 and 14) showed potent inhibition toward α-glucosidase with IC₅₀ values in the range 0.4-26.6 μM. Calodenin A (15) was the most active compound with an IC₅₀ value of 0.4 μM (the positive control, acarbose, IC₅₀ 93.6 μM). A kinetic analysis of 15 revealed that it is a noncompetitive inhibitor with a K_i value of 3.4 μM.