Natural compound cudraflavone B shows promising anti-inflammatory properties in vitro.

Article Details

Citation

Hosek J, Bartos M, Chudik S, Dall'Acqua S, Innocenti G, Kartal M, Kokoska L, Kollar P, Kutil Z, Landa P, Marek R, Zavalova V, Zemlicka M, Smejkal K

Natural compound cudraflavone B shows promising anti-inflammatory properties in vitro.

J Nat Prod. 2011 Apr 25;74(4):614-9. doi: 10.1021/np100638h. Epub 2011 Feb 14.

PubMed ID
21319773 [ View in PubMed
]
Abstract

Cudraflavone B (1) is a prenylated flavonoid found in large amounts in the roots of Morus alba, a plant used as a herbal remedy for its reputed anti-inflammatory properties. The present study shows that this compound causes a significant inhibition of inflammatory mediators in selected in vitro models. Thus, 1 was identified as a potent inhibitor of tumor necrosis factor alpha (TNFalpha) gene expression and secretion by blocking the translocation of nuclear factor kappaB (NF-kappaB) from the cytoplasm to the nucleus in macrophages derived from a THP-1 human monocyte cell line. The NF-kappaB activity reduction resulted in the inhibition of cyclooxygenase 2 (COX-2) gene expression. Compound 1 acts as a COX-2 and COX-1 inhibitor with higher selectivity toward COX-2 than indomethacin. Pretreatment of cells by 1 shifted the peak in an regulatory gene zinc-finger protein 36 (ZFP36) expression assay. This natural product has noticeable anti-inflammatory properties, suggesting that 1 potentially could be used for development as a nonsteroidal anti-inflammatory drug lead.

DrugBank Data that Cites this Article

Binding Properties
DrugTargetPropertyMeasurementpHTemperature (°C)
IndomethacinProstaglandin G/H synthase 2IC 50 (nM)1900N/AN/ADetails