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1.
Chem Biodivers ; 17(2): e1900609, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31916412

ABSTRACT

The fruit of Crataegus dahurica Koehne was used to treat the disease of infantile indigestion and dyspepsia as an ethnic medicine and food. As a continuous work on finding the active constituents from the edible herbs, four new biphenyl derivatives (1-4), together with two known compounds (5 and 6), were obtained from the petroleum ether fraction of the fruits of C. dahurica. Their structures were determined by the extensive 1D and 2D NMR spectra and HR-MS spectrometry. Furthermore, the anti-inflammatory activities of all the isolated compounds were investigated, in which compound 4 showed moderately inhibitory effects on NO production in RAW264.7 cells without inducing cytotoxicity.


Subject(s)
Anti-Inflammatory Agents/chemistry , Crataegus/chemistry , Animals , Anti-Inflammatory Agents/isolation & purification , Anti-Inflammatory Agents/pharmacology , Biphenyl Compounds/chemistry , Biphenyl Compounds/isolation & purification , Biphenyl Compounds/pharmacology , Cell Survival/drug effects , Crataegus/metabolism , Fruit/chemistry , Fruit/metabolism , Lipopolysaccharides/toxicity , Macrophages/cytology , Macrophages/drug effects , Macrophages/metabolism , Magnetic Resonance Spectroscopy , Mice , Molecular Conformation , Nitric Oxide/metabolism , RAW 264.7 Cells
2.
Chem Biodivers ; 16(1): e1800424, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30387325

ABSTRACT

Continually phytochemical study of the roots of Heracleum dissectum had led to the isolation of three previously undescribed polyacetylene glycosides (1-3), together with seven known compounds, including one polyacetylene (8) and six coumarins (4-7 and 9-10) using diverse chromatographic methods. The structures of these three new compounds were characterized and identified as deca-4,6-diyn-1-yl ß-d-glucopyranosyl-(1→6)-ß-d-glucopyranosyl-(1→2)-ß-d-glucopyranoside (1), (8Z)-dec-8-ene-4,6-diyn-1-yl ß-d-glucopyranosyl-(1→6)-ß-d-glucopyranosyl-(1→2)-ß-d-glucopyranoside (2), and (8E)-dec-8-ene-4,6-diyn-1-yl ß-d-glucopyranosyl-(1→6)-ß-d-glucopyranosyl-(1→2)-ß-d-glucopyranoside (3) based on their physicochemical properties and extensive analyses of various spectroscopic data. Their triglycerides accumulating activities were assayed and the results showed that the three new polyacetylene glycosides (1-3) exhibited triglyceride accumulating activities in 3T3-L1 adipocytes.


Subject(s)
Glycosides/isolation & purification , Glycosides/pharmacology , Heracleum/chemistry , Plant Extracts/pharmacology , Plant Roots/chemistry , Polyacetylene Polymer/chemistry , Triglycerides/metabolism , 3T3-L1 Cells , Animals , Carbohydrate Conformation , Carbon-13 Magnetic Resonance Spectroscopy , Glycosides/chemistry , Methanol/chemistry , Mice , Plant Extracts/chemistry , Proton Magnetic Resonance Spectroscopy , Spectrometry, Mass, Electrospray Ionization
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