Authors: Hsu Y.M., Wu T.Y., Du Y.C., El-Shazly M.,
Beerhues L., Thang T.D.,
Van Luu H., Hwang T.L., Chang F.R., Wu Y.C.
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Abstract: The
phytochemical investigation of the methanolic extract of Uvaria flexuosa
(Annonaceae) leaves led to the isolation of seven compounds including,
3-methyl-4,5-dihydro-oxepine (flexuvaroxepine A), four polyoxygenated
seco-cyclohexene (flexuvarin A–D) and two polyoxygenated cyclohexene
(flexuvarol A–B) derivatives, together with four known flavones. The
structures of the isolated compounds were elucidated using different
spectroscopic techniques. A plausible biogenetic route of the new compounds
was discussed. The anti-inflammatory activity of the isolated compounds was
evaluated by superoxide anion generation and elastase release assays. Among
the tested compounds, flexuvarol B and chrysin showed the most potent
anti-inflammatory effect by inhibiting superoxide anion generation and
elastase release from human neutrophils in response to fMLP with IC50
2.25–5.55 μM. Moreover, 5-hydroxy-6,7-dimethoxy-flavone showed selective
inhibitory activity on superoxide anion generation (IC50 = 1.19 ± 0.34 μM).
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