ABSTRACT
The fruits of Eucalyptus globulus Labill. are known to have a plenty of medicinal properties, such as anti-tumor, anti-inflammatory, and immunosuppressive activity. Our previous study found that the phloroglucinol-sesquiterpene adducts in the fruits of E. globulus were immunosuppressive active constituents, especially Eucalyptin C (EuC). Phosphoinositide 3-kinases-γ (PI3Kγ) plays a pivotal role in T cell mediated excessive immune responses. In this study, EuC was first discovered to be a novel selective PI3Kγ inhibitor with an IC
Subject(s)
Animals , Mice , Eucalyptus , Flavonoids , Fruit , Molecular Docking Simulation , Phosphoinositide-3 Kinase InhibitorsABSTRACT
@#A qualitative analytical method of liquid chromatography coupled with mass spectrometry(LC-MSn)was developed for the identification of main constituents in Chrysanthemum morifolium ‘Fubaiju’. High-performance liquid chromatography(HPLC)was developed for the quantification of five active components, including chlorogenic acid(1), luteolin-7-O-β-D-glucopyranoside(2), luteolin-7-O-β-D-glucopyranuronide(3), 3, 5-Di-caffeoylquinic acid(4), and apigenin-7-O-β-D-glucopyranoside(5). A total of 22 compounds, including 13 flavonoids and 9 phenolic acids, were identified based on their retention behaviors, UV profiles and MS fragment information. Furthermore, a validation method with good linearity(r> 0. 999 9), precision, stability, repeatability and recovery was successfully applied for simultaneous determination of five major components in 10 batches of C. morifolium ‘Fubaiju’ by HPLC-UV method. The established method was proved to be a validation strategy for the quality evaluation of C. morifolium ‘Fubaiju’.
ABSTRACT
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.
Subject(s)
Anti-Inflammatory Agents , Chemistry , Cyclooxygenase 1 , Chemistry , Cyclooxygenase 2 , Chemistry , Cyclooxygenase Inhibitors , Chemistry , Flavonoids , Chemistry , Molecular Structure , Myrtaceae , Chemistry , Plant Components, Aerial , Chemistry , Plant Extracts , ChemistryABSTRACT
@#Phytochemical studies on the fruits of Eucalyptus globulus led to the isolation of twelve compounds. The structures of these compounds were elucidated as: ellagic acid(1), 3-O-methylellagic acid 4′-O-α-rhamnopyranoside(2), valoneic acid dilactone(3), isobiflorin(4), biflorin(5), 8-β-C-glucopyranosyl-5, 7-dihydroxy-2-isobutylchromone(6), 8-β-C-glucopyranosyl-5, 7-dihydroxy-2-isopropylchromone(7), quercetin 3-O-β-D-glucopyranoside(8), quercetin 3-O-β-D-glucuronide-6″-methyl ester(9), (+)-lyoniresin-4-yl β-D-glucopyranoside(10), cypellocarpins A(11), and eucaglobulin 1(12), by means of spectroscopic analyses(ESI-MS, 1H NMR and 13C NMR). Compounds 3-10 were isolated from this plant for the first time.
ABSTRACT
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.