Química Nova (Jan 2014)

Isolation and antitrichomonal activity of the chemical constituents of the leaves of Maytenus phyllanthoides Benth. (Celastraceae)

  • Juan Alberto Moo-Puc,
  • Zhelmy Martín-Quintal,
  • Gumersindo Mirón-López,
  • Rosa Esther Moo-Puc,
  • Leovigildo Quijano,
  • Gonzalo J. Mena-Rejón

DOI
https://doi.org/10.1590/S0100-40422014000100016
Journal volume & issue
Vol. 37, no. 1
pp. 85 – 88

Abstract

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Cyclolignan (+)-lyoniresinol (1), veratric acid (2), vanillic acid (3), lupeol, oleanolic acid, 3β-hydroxy-urs-11-en-28,13β-lactone (4), the mixture of α- and β-amyrin, trans-polyisoprene, and β-sitosterol were isolated from the leaves of Maytenus phyllanthoides. The structures of the isolated compounds were established based on spectroscopic data, mainly ¹H and 13C nuclear magnetic resonance (NMR). Compound 1, its acetate analog 1a, and compounds 2, 3, and 4 were tested against Trichomonas vaginalis. (+)-Lyoniresinol showed activity corresponding to IC50 17.57 µM. This is the first report on the occurrence of 3β-hydroxy-urs-11-en-28,13β-lactone (4) in the Celastraceous family and lyoniresinol in the Maytenus genus, and on the antitrichomonal activity of lyoniresinol.

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