Alpha-glucosidase inhibitory activity of Aeschynanthus maculatus.
- Author:
Pu-yu TIAN
1
;
Wen-yi KANG
Author Information
- Publication Type:Journal Article
- MeSH: Enzyme Inhibitors; chemistry; pharmacology; Ferns; chemistry; Glycoside Hydrolase Inhibitors; Plant Exudates; chemistry; pharmacology
- From: China Journal of Chinese Materia Medica 2012;37(19):2910-2912
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the inhibitory activity of Aeschynanthus maculatus on alpha-glucosidase.
METHODThe inhibilitory model of in vitro alpha-glucosidase was established. Active extracts of A. maculatus were isolated and identified bymultiple chromatographic methods, and their molecular structures were identifiied by spectral techniques.
RESULTSeven coumpounts were isolated from A. maculatus and isolated as lupeol(1), stigmasterol(2), ursolic acid(3), stigmast-5,22(E)-diene-3beta-ol(4), beta-daucosterol(5), 3-hydroxy-12-taraxasten-28-oic-acid(6) and oleanic acid(7). Compounds 1 (IC50 25.41 mg x L(-1)),3(IC0 4.42 mg L(-1)),4(IC50 11.50 mg x L(-1)),6(IC50 14.17 mg x L(-1)) and 7(IC50 2.88 mg x L(-1)) had higher inhibitory activities than that of acarbose (IC50 1103.01 mg x L(-1)) as the positive control drug.
CONCLUSIONCompound 1-7 were isolated from this plant for the first time. Compound 6 was isolated from Gesneriaceae family for the first time. Compound 7 was isolated from Aeschynanthus genus for the first time.