Journal
JOURNAL OF NATURAL PRODUCTS
Volume 71, Issue 11, Pages 1934-1937Publisher
AMER CHEMICAL SOC
DOI: 10.1021/np800134h
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Funding
- University of Athens
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Phytochemical investigation of a methanol extract of Onobrychis ebenoides yielded five new 3-formyl-2-arylbenzofurans, namely, ebenfurans IV-VII (1-5), together with the known compounds ebenfurans I, II (6), and III (7). Only 1 and 7 exhibited growth inhibitory activity against MCF-7 and Ishikawa cells, suggesting that the prenyl moiety at position C-5 is the key determinant of the cytotoxic activity of this group of compounds.
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