Two new glycosides, ethyl-O-β-D-furanosyl-(1→6)-O-β-D-glucopyranoside (1) and (5-′′)-galloyl-ethyl-O-β-D-furanosyl-(1→6)-O-β-D-glucopyranoside (2), together with eight known compounds (3–10) were obtained from the n-BuOH extraction of Paeonia ostii. Their structures were identified via the extensive spectroscopic analysis. Compounds 1, 3–10 exhibited the anti-inflammation activities, which inhibited the production of NO, TNF-α and IL-1β in LPS-induced RAW264.7 cells with IC50 values ranging from 6.00 to 86.78 µΜ.
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Kong et al. (2024) studied this question.
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