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Phytochemistry ; 103: 129-136, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-24746259

RESUMO

Seven acylated flavonol glycosides named elaeagnosides A-G, in addition to seven known flavonoids were isolated from the flowers of Elaeagnus angustifolia. Their structures were elucidated by different spectroscopic methods including 1D, 2D NMR experiments and HR-ESI-MS analysis. In order to identify natural antioxidant and tyrosinase inhibitor agents, the abilities of these flavonoids to scavenge the 1,1-diphenyl-2-picrylhydrazyl radical (DPPH) and to inhibit tyrosinase activity were evaluated. Results revealed that two of these compounds had significant anti-oxidant effect and one compound showed weak tyrosinase-inhibitory activity compared with kojic acid, quercetin, or ascorbic acid, which were used as positive control.


Assuntos
Elaeagnaceae/química , Flavonóis/química , Flores/química , Glicosídeos/química , Acilação , Antioxidantes/química , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Monofenol Mono-Oxigenase/antagonistas & inibidores
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