1. Academic Validation
  2. Weakly antimalarial flavonol arabinofuranosides from Calycolpus warszewiczianus

Weakly antimalarial flavonol arabinofuranosides from Calycolpus warszewiczianus

  • J Nat Prod. 2006 May;69(5):826-8. doi: 10.1021/np050484i.
Daniel Torres-Mendoza 1 José González Eduardo Ortega-Barría María V Heller Todd L Capson Kerry McPhail William H Gerwick Luis Cubilla-Rios
Affiliations

Affiliation

  • 1 Laboratory of Tropical Bioorganic Chemistry, Faculty of Natural, Exact Sciences and Technology, University of Panama, Panama City, Republic of Panama.
Abstract

Three new flavonol arabinosides (2-4) were isolated from the young leaves of Calycolpus warszewiczianus. The structures were determined as myricetin-3-O-alpha-L-3' '-acetylarabinofuranoside (2), myricetin-3-O-alpha-L-3' ',5' '-diacetylarabinofuranoside (3), and 5-galloylquercetin-3-O-alpha-L-arabinofuranoside (4). Molecular structures were elucidated using NMR spectroscopy in combination with IR and MS data. Two known compounds, myricetin-3-O-alpha-L-arabinofuranoside (1) and (-)-epi-catechin (5), were also isolated. The compounds were tested in vitro against a chloroquine-resistant strain of Plasmodium falciparum, Leishmania mexicana, and Trypanosoma cruzi parasites. Compound 4 demonstrated weak activity against a chloroquine-resistant strain of P. falciparum (14.5 microM), whereas none of the compounds demonstrated activity against L. mexicana and T. cruzi at the concentrations of 40 and 50 microg/mL, respectively, and no cytotoxicity was detected against mammalian cells below 100 microg/mL.

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