Molecules (Feb 2007)

Reactive Oxygen Species Scavenging Activity of Flavone Glycosides from Melilotus neapolitana

  • Pietro Monaco,
  • Palma Oriano,
  • Claudio Mastellone,
  • Annunziata Golino,
  • Severina Pacifico,
  • Brigida D'Abrosca,
  • Antonio Fiorentino

DOI
https://doi.org/10.3390/12020263
Journal volume & issue
Vol. 12, no. 2
pp. 263 – 270

Abstract

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One new and six known flavone glycosides were isolated from the MeOH extract of Melilotus neapolitana Ten. The new compound, identified as 7-O-β-D-gluco-pyranosyloxy-4',5-dihydroxy-3-[O-α-L-rhamnopyranosyl-(1→6)-3-O-β-D-glucopyrano-syloxy]flavone (1) by 1D and 2D NMR techniques and mass spectra, was isolated along with kaempferol-3-O-rutinoside (2), kaempferol-3-O-glucoside (3), rutin (4), quercetin-3-O-glucoside (5), isorhamnetin-3-O-rutinoside (6), and isorhamnetin-3-O-glucoside (7). The antioxidant and radical scavenging activities of these compounds and the whole crude methanol extract were evaluated. The organic extract can inhibit MDA marker’s synthesis by 57%. All the metabolites displayed good reducing power, with the kaempferol (2,3) and isorhamnetin derivatives (6,7) being less active than the corresponding quercetin derivatives 4,5.

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