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Phenolic Derivatives from Fruits of Dipteryx lacuniferaDucke and Evaluation of Their Antiradical Activities

✍ Scribed by Gerardo Magela V. Júnior; Cleyton Marcos de M. Sousa; Alberto J. Cavalheiro; João Henrique G. Lago; Mariana H. Chaves


Publisher
John Wiley and Sons
Year
2008
Tongue
German
Weight
246 KB
Volume
91
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

The fruits of Dipteryx lacunifera, known as ‘fava de morcego’ and ‘garampara’, comprise pleasant tasting kernels that contain high amounts of fatty acids (mainly oleic acid) and are commonly consumed by inhabitants of the northeast of Brazil. In the present study, the crude EtOH extract of the fruit kernels was separated into hexane‐, Et~2~O‐, AcOEt‐, and H~2~O‐soluble fractions. The Et~2~O fraction was found to exhibit the highest 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) radical‐scavenging activity in vitro, and was subjected to further fractionation. Column chromatography over silica gel and Sephadex LH‐20, followed by preparative HPLC‐C~18~, afforded (−)‐eriodictyol (1), (−)‐butin (2), luteolin (3), 3′,4′,7‐trihydroxyflavone (4), butein (5), and sulfuretin (6). The antiradical activities of compounds 1, 2, 4, and 6, together with the positive controls rutin, butylated hydroxy toluene (BHT), and tert‐butylhydroquinone (TBHQ), were evaluated with the DPPH assay and were found to decrease in the order rutin>4>1>6>2>TBHQ>BHT.


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