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1.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 615-620, 2018.
Artículo en Inglés | WPRIM | ID: wpr-812368

RESUMEN

In the present study, we carried out a phytochemical investigation of the ethanol extract of the aerial parts of Baeckea frutescens, which resulted in the isolation of two new flavonoid glycosides, myricetin 3-O-(5″-O-galloyl)-α-L-arabinofuranoside (1), 6-methylquercetin 7-O-β-D-glucopyranoside (2), one new methylchromone glycoside, 7-O-(4', 6'-digalloyl)-β-D-glucopyranosyl-5-hydroxy-2-methylchromone (3), together with three known compounds (4-6). The structures of these isolated compounds were established on the basis of 1D and 2D NMR techniques and chemical methods. The anti-inflammatory activities of the compounds 1-6 were evaluated for their inhibitory effects against cyclooxygenases-1 and -2 in vitro. Compounds 1-6 showed potent COX-1 and COX-2 inhibiting activities in vitro with IC values ranging from 1.95 to 5.54 μmol·L and ranging from 1.01 to 2.27 μmol·L, respectively.


Asunto(s)
Antiinflamatorios , Química , Ciclooxigenasa 1 , Química , Ciclooxigenasa 2 , Química , Inhibidores de la Ciclooxigenasa , Química , Flavonoides , Química , Estructura Molecular , Myrtaceae , Química , Componentes Aéreos de las Plantas , Química , Extractos Vegetales , Química
2.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 615-620, 2018.
Artículo en Inglés | WPRIM | ID: wpr-773579

RESUMEN

In the present study, we carried out a phytochemical investigation of the ethanol extract of the aerial parts of Baeckea frutescens, which resulted in the isolation of two new flavonoid glycosides, myricetin 3-O-(5″-O-galloyl)-α-L-arabinofuranoside (1), 6-methylquercetin 7-O-β-D-glucopyranoside (2), one new methylchromone glycoside, 7-O-(4', 6'-digalloyl)-β-D-glucopyranosyl-5-hydroxy-2-methylchromone (3), together with three known compounds (4-6). The structures of these isolated compounds were established on the basis of 1D and 2D NMR techniques and chemical methods. The anti-inflammatory activities of the compounds 1-6 were evaluated for their inhibitory effects against cyclooxygenases-1 and -2 in vitro. Compounds 1-6 showed potent COX-1 and COX-2 inhibiting activities in vitro with IC values ranging from 1.95 to 5.54 μmol·L and ranging from 1.01 to 2.27 μmol·L, respectively.


Asunto(s)
Antiinflamatorios , Química , Ciclooxigenasa 1 , Química , Ciclooxigenasa 2 , Química , Inhibidores de la Ciclooxigenasa , Química , Flavonoides , Química , Estructura Molecular , Myrtaceae , Química , Componentes Aéreos de las Plantas , Química , Extractos Vegetales , Química
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