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Natural Product Research
Formerly Natural Product Letters
Volume 30, 2016 - Issue 4
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Articles

Cytotoxity of two new coumarin derivatives isolated from Launaea mucronata

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Pages 394-398 | Received 23 Dec 2014, Accepted 05 Feb 2015, Published online: 09 Mar 2015
 

Abstract

The chloroform fraction of methanol (MeOH) extract of the aerial parts of Launaea mucronata was in vitro investigated for cytotoxicity against HCT116, HepG2 and MCF-7 cell lines, and resulted with IC50 = 20.0, 18.6 and 14.30 μg/mL, respectively. The chloroform fraction of the MeOH extract was subjected to further fractionation, which led to the isolation of two new coumarin compounds (6-isobutyl coumarin and 6-isobutyl-7-methyl- coumarin). The structures of the new compounds were elucidated by high field 1D and 2D NMR and ESI-MS spectroscopies. Low polar fractions revealed the isolation of other known triterpene compounds which were identified according to its spectral data and comparison with the literature. New coumarin compounds show high cytotoxicity against MCF-7, HCT116 and HepG2 cell lines.

Acknowledgements

The authors are thankful to the Bioassay-Cell Culture Laboratory, National Research Centre, El-Tahrir St., Dokki, Cairo 12622, Egypt for conducting the analysis and determining the results.

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