Química Nova (Jan 2009)

First secondary metabolites from Herissantia crispa L (Brizicky) and the toxicity activity against Artemia salina Leach

  • Danielly Albuquerque da Costa,
  • Wemerson Neves Matias,
  • Igara Oliveira Lima,
  • Aline Lira Xavier,
  • Vivian Bruna Machado Costa,
  • Margareth de Fátima Formiga Melo Diniz,
  • Maria de Fátima Agra,
  • Leônia Maria Batista,
  • Maria de Fátima Vanderlei de Souza,
  • Davi Antas e Silva

DOI
https://doi.org/10.1590/S0100-40422009000100009
Journal volume & issue
Vol. 32, no. 1
pp. 48 – 50

Abstract

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The phytochemical investigation of Herissantia crispa led to the isolation of seven compounds, identified as: sitosterol 3-O-β-D-glucopyranoside, stigmasterol 3-O-β-D-glucopyranoside, 3,5,7,4'-tetrahydroxyflavone (kaempferol), 3,5,7,3',4'-pentahydroxyflavone (quercetin), unpublished in the genus Herissantia, besides β-sitosterol, kaempferol 3-O-β-D-(6''-E-p-coumaroil) (tiliroside) glucopyranoside and kaempferol 3,7-di-O-α-L-ramnopyranoside (lespedin), described for the first time in the species. The structural determination of the compounds was made by means of spectroscopy methods such as Infrared Spectroscopy, ¹H and 13C Nuclear Magnetic Resonance, with the aid of two dimensional techniques, and by comparison with literature data. The toxicity activity of the MeOH extract and lespedin on Artemia salina Leach. was also carried out.

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