RESUMEN
OBJECTIVE: To study the chemical constituents of Paeonia lactiflora flowers. METHODS: [corrected] The chemical constituents were isolated and purified by various chromatography methods,and the structures were identified by physicochemical and modem spectroscopic. RESULTS: 11 compounds were identified as gallic acid(1),methyl gallate(2),ethyl gallate(3),1,2,3,6-tetragalloyl-beta-D-glucopyranoside(4), 1,2,3,4,6-pentagalloyl-beta-D-glucopyranoside(5), quercetin-3-O-glucoside-6"-gallate(6), kaempferol-3-O-glucoside-6"-gallate(7), 1-O-galloyl-beta-D-glucose (8), kaempferol-3, 7-di-O-beta-D-glucoside(9), paeoniflorin(10) and albiflorin(11). CONCLUSIONS: Compounds 1-8, 10 and 11 are obtained from the flowers of Paeonia lactiflora for the first time,compounds 6 and 7 are obtained from Paeonia genus for the first time.
Asunto(s)
Medicamentos Herbarios Chinos/química , Flores/química , Paeonia/química , Plantas Medicinales/química , Hidrocarburos Aromáticos con Puentes/química , Hidrocarburos Aromáticos con Puentes/aislamiento & purificación , Cromatografía Líquida de Alta Presión , Medicamentos Herbarios Chinos/aislamiento & purificación , Glucósidos/química , Glucósidos/aislamiento & purificación , Quempferoles/química , Quempferoles/aislamiento & purificación , Estructura Molecular , Monosacáridos/química , Monosacáridos/aislamiento & purificación , Monoterpenos/química , Monoterpenos/aislamiento & purificaciónRESUMEN
This study aimed to seek an efficient method to extract and purify yunaconitine and 8-deacetylyunaconitine from Aconitum vilmorinianum Kom. by accelerated solvent extraction combined with pH-zone-refining counter-current chromatography. The major extraction parameters for accelerated solvent extraction were optimized by an orthogonal test design L9 (3)(4). Then a separation and purification method was established using pH-zone-refining counter-current chromatography with a two-phase solvent system composed of petroleum ether/ethyl acetate/methanol/water (5:5:2:8, v/v) with 10 mM triethylamine in the upper phase and 10 mM HCl in the lower phase. From 2 g crude extract, 224 mg of 8-deacetylyunaconitine (I) and 841 mg of yunaconitine (II) were obtained with a purity of over 98.0%. The chemical structures were identified by ESI-MS and (1)H and (13)C NMR spectroscopy.