Planta Med 2010; 76(7): 708-712
DOI: 10.1055/s-0029-1240627
Natural Product Chemistry
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Cytotoxicity of Natural Compounds Isolated from the Seeds of Garcinia afzelii

Alain Meli Lannang1 , 2 , Gabin Nselapi Louh3 , Bernadette Messi Biloa3 , Justin Komguem3 , Celine Djama Mbazoa3 , Beiban Luc Sondengam3 , Lieve Naesens4 , Christophe Pannecouque4 , Erik De Clercq4 , El H. Sayed El Ashry2
  • 1Department of Chemistry, Higher Teachers' Training College, University of Maroua, Maroua, Cameroon
  • 2Department of Chemistry, Faculty of Science, Alexandria University, Alexandria, Egypt
  • 3Department of Organic Chemistry, Faculty of Science, University of Yaoundé I, Yaoundé, Cameroon
  • 4Rega Institute for Medical Research, Leuven, Belgium
Further Information

Publication History

received June 3, 2009 revised October 23, 2009

accepted October 29, 2009

Publication Date:
20 November 2009 (online)

Abstract

The new compounds guttiferone O (1) and 3-methoxycheffouxanthone (2) have been isolated from the seeds of Garcinia afzelii Engl., together with nine known compounds: 2-hydroxy-1,7-dimethoxyxanthone (3), smeathxanthone A (4), 1,5-dihydroxyxanthone (5), 1,6-dihydroxy-5-methoxyxanthone (6), cheffouxanthone (7), 1,3,5-trihydroxyxanthone (8), smeathxanthone B (9), isoxanthochymol (10) and guttiferone E (11). Their structures were elucidated by means of 1D and 2D‐NMR techniques. All the isolates showed high cytotoxic activity and were found inactive when tested against HIV and influenza viruses.

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Prof. El-Sayed H. El-Ashry

Department of Chemistry
Faculty of Science
Alexandria University

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