The leaves of Chromolaena odorata (Asteraceae) are exploited extensively in West and Central African ethnopharmacy for the treatment of a wide range of conditions, despite this being a non-native species established in the last 50 years. With the objective of seeking bioactive principles, the nonvolatile compounds, an ethanolic (80% v/v) extract was made and fractionated. From the hexane-soluble fraction, three compounds were isolated. Two of these, 5-hydroxy-7,4′-dimethoxyflavanone and 2′-hydroxy-4,4′, 5′,6′-tetramethoxychalcone, have previously been identified in C. odorata leaves. The third was fully characterised spectroscopically and found to be 1,6-dimethyl-4-(1-methylethyl)naphthalene (cadalene), not previously isolated from the Asteraceae. All three compounds were tested for their cytotoxicity and anticancer properties. 2′-Hydroxy-4,4′,5′, 6′-tetramethoxychalcone was found to be both cytotoxic and anticlonogenic at 20 μm in cell lines Cal51, MCF7 and MDAMB-468, and to act synergistically with the Bcl2 inhibitor ABT737 to enhance apoptosis in Cal51 breast cancer cells. Copyright © 2012 John Wiley & Sons, Ltd.
CITATION STYLE
Kouamé, P. B. K., Jacques, C., Bedi, G., Silvestre, V., Loquet, D., Barillé-Nion, S., … Tea, I. (2013). Phytochemicals isolated from leaves of chromolaena odorata: Impact on viability and clonogenicity of cancer cell lines. Phytotherapy Research, 27(6), 835–840. https://doi.org/10.1002/ptr.4787
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