Separation of ethyl acetate fractionation of Dracocephalum peregrinum afforded three new flavonoid glucosides (1-3), and a new cyanogenic glucoside (4). Their structures were elucidated based on HR-electron spray ionization (ESI)-MS, EI-MS, UV, IR, 1D-, and 2D-NMR data. 1-4 were tested in vitro for their antiinflammatory activity against the RAW 264.7, 293 cells. Among the compounds tested, 1-4 shown good antiinflammatory activity at 100 μg/ml by the measurement of nitric oxide (NO) in lipopolysaccharide (LPS) activated macrophages. But only 2 and 3 shown weak antiinflammatory activity at 100 μg/ml during the nuclear factor (NF)-κB activation assay. © 2009 Pharmaceutical Society of Japan.
CITATION STYLE
Fu, P., Zhao, C. C., Tang, J., Shen, Y. H., Xu, X. K., & Zhang, W. D. (2009). New flavonoid glycosides and cyanogenic glycosides from dracocephalum peregrinum. Chemical and Pharmaceutical Bulletin, 57(2), 207–210. https://doi.org/10.1248/cpb.57.207
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