Abstract
Bioassay-guided fractionation of the ethyl acetate extract of the roots of Dalea scandens (Miller) R. Clausen var. paucifolia led to the isolation of new flavonoids, 2(S )-5′-(-1′″,1″′-dimethylallyl)-8-(3″,3″-dimethylallyl)-2′,4′,5,7-tetrahydroxyflavanone, 2(S )-5′-(1″′,1″′-dimethylallyl)-8-(3″,3″-dimethylallyl)-2′-methoxy-4′,5,7-trihydroxyflavanone and 5′-(1″′,1″′-dimethylallyl)-8-(3″,3″-dimethylallyl)-2′,4′,5,7-tetrahydroxyflavone. Structure elucidation was carried out by spectroscopic methods. All three compounds showed significant activity against both methicillin-susceptible and methicillin-resistant Staphylococcus aureus.
Key words
Dalea scandens var. paucifolia
- Fabaceae - prenylated flavonoids - methicillin-resistant Staphylococcus aureus
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N. P. Dhammika Nanayakkara
National Center for Natural Products Research
School of Pharmacy
The University of Mississippi
University
MS 38677, USA
Fax: +1-662-915-7989
Email: dhammika@olemiss.edu