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α-Glucosidase inhibitory caged xanthones from the resin of Garcinia hanburyiopen access

Authors
Jin, Y.M.Kim, J.Y.Lee, S.M.Tan, X.F.Park, K.H.
Issue Date
2019
Publisher
Korean Society for Applied Biological Chemistry
Keywords
Caged xanthones; Gambogoic acid; Garcinia hanburyi; Noncompetitive inhibition; α-Glucosidase
Citation
Journal of Applied Biological Chemistry, v.62, no.1, pp 81 - 86
Pages
6
Indexed
SCOPUS
KCI
Journal Title
Journal of Applied Biological Chemistry
Volume
62
Number
1
Start Page
81
End Page
86
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/10659
DOI
10.3839/jabc.2019.012
ISSN
1976-0442
2234-7941
Abstract
A yellow resin (gamboge) from Garcinia hanburyi has been widely used as folk medicine due to its antibacterial and antitumor activities. We isolated four a-glucosidase inhibitory compounds from the methanol extract of gamboge. The compounds (1-4) were identified as gambogoic acid (1), moreollic acid (2), gambogic acid (3), and 10-methoxygambogenic acid (4), respectively through spectroscopic data including 2D-NMR and HREIMS. All compounds were examined in the enzyme inhibition assay against a-glucosidase to identify their inhibitory potencies and kinetic behavior. All compounds (1-4) showed enzyme inhibition against a-glucosidase, but the activity was significantly affected by the methoxy group on C-10 of ring A and pentenyl pyran moiety of ring D. For example, compound 1 (IC 50 =41.4 ?M) bearing pyran ring eight times effective that 4 (IC 50 =350.6 ?M) having geranyl group itself. Most active compound was found out to be gambogoic acid (1) which was analyzed most abundant metabolite in gamboge by LC-ESI-MS/MS. In kinetic study, compounds 1 and 2 were proved as noncompetitive inhibitors. ? The Korean Society for Applied Biological Chemistry 2019.
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