Planta Med 2012; 78(16): 1777-1779
DOI: 10.1055/s-0032-1315256
Letters
Georg Thieme Verlag KG Stuttgart · New York

Pyrone and Unusually Furanone-substituted Flavones from the Leaves of Hoslundia opposita

Rim Salame
1   Chimie des Substances Naturelles, CNRS UMR 8076 BioCIS, Labex LERMIT, Faculté de Pharmacie, Université Paris-Sud, Châtenay-Malabry, France
,
Zakaria Cheikh-Ali
1   Chimie des Substances Naturelles, CNRS UMR 8076 BioCIS, Labex LERMIT, Faculté de Pharmacie, Université Paris-Sud, Châtenay-Malabry, France
,
Christian Bories
2   Chimiothérapie Antiparasitaire, CNRS UMR 8076 BioCIS, Labex LERMIT, Faculté de Pharmacie, Université Paris-Sud, Châtenay-Malabry, France
,
Marcelline Adiko
1   Chimie des Substances Naturelles, CNRS UMR 8076 BioCIS, Labex LERMIT, Faculté de Pharmacie, Université Paris-Sud, Châtenay-Malabry, France
3   Laboratoire de Pharmacologie, Pharmacie Clinique, Thérapeutique et Physiologie, UFR Sciences Pharmaceutiques et Biologiques, Université Cocody-Abidjan, Abidjan, République de Côte dʼIvoire
,
Erwan Poupon
1   Chimie des Substances Naturelles, CNRS UMR 8076 BioCIS, Labex LERMIT, Faculté de Pharmacie, Université Paris-Sud, Châtenay-Malabry, France
,
Pierre Champy
1   Chimie des Substances Naturelles, CNRS UMR 8076 BioCIS, Labex LERMIT, Faculté de Pharmacie, Université Paris-Sud, Châtenay-Malabry, France
› Author Affiliations
Further Information

Publication History

received 25 April 2012
revised 20 July 2012

accepted 24 July 2012

Publication Date:
04 September 2012 (online)

Abstract

Two new unusual 6-furanoflavones, hoslunfuranine (5) and 5-O-methylhoslunfuranine (6), were isolated from the leaves of Hoslundia opposita Vahl.. Four known methylpyranoflavonic analogues [hosloppin (1), hoslundin (2), 5-O-methylhoslundin (3), oppositin (4)], all specific of the species, were also obtained. Their structures were established on the basis of their spectroscopic data. In vitro cytotoxic, trypanocidal, and leishmanicidal activities of compounds 1 and 3 to 6 were evaluated. Compounds 4 and 6 exhibited leishmanicidal potential in the micromolar range.

Supporting Information

 
  • References

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