Planta Med 2008; 74(8): 870-872
DOI: 10.1055/s-2008-1074546
Natural Products Chemistry
Letter
© Georg Thieme Verlag KG Stuttgart · New York

Further Studies of the Norditerpene (+)-Harringtonolide Isolated from Cephalotaxus harringtonia var. drupacea: Absolute Configuration, Cytotoxic and Antifungal Activities

Laurent Evanno1 , Akino Jossang1 , Julie Nguyen-Pouplin1 , Diane Delaroche2 , Patrick Herson3 , Mannan Seuleiman3 , Bernard Bodo1 , Bastien Nay1
  • 1Laboratoire de Chimie et Biochimie des Substances Naturelles, Muséum National d′Histoire Naturelle, CNRS, Paris, France
  • 2Laboratoire de Synthèse, Structure et Fonction de Molécules Bioactives, Université Pierre et Marie Curie, CNRS, Paris, France
  • 3Laboratoire de Chimie Inorganique et Matériaux Moléculaires, Université Pierre et Marie Curie, CNRS, Paris, France
Further Information

Publication History

Received: January 28, 2008 Revised: April 14, 2008

Accepted: April 19, 2008

Publication Date:
03 June 2008 (online)

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Abstract

Harringtonolide (= hainanolide) is a complex polycyclic fused norditerpene isolated from Cephalotaxus harringtonia var. drupacea. In spite of its appealing biological properties – we measured an IC50 of 43 nM on KB cells and a significant antifungal activity – its absolute configuration has not yet been firmly established. This was done herein using X-ray anomalous scattering after bromination of the tropone ring, unambiguously giving the stereochemistry 5R,6R,7S,13S,14S,15R,16R. Detailed in vitro biological measurements are provided.

References

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