Planta Med 2002; 68(11): 1042-1044
DOI: 10.1055/s-2002-35651
Letter
© Georg Thieme Verlag Stuttgart · New York

Cytotoxic Aporphine Alkaloids from Cassytha filiformis

C. Stévigny1 , S. Block1 , M. C. De Pauw-Gillet2 , E. de Hoffmann3 , G. Llabrès4 , V. Adjakidjé5 , J. Quetin-Leclercq1
  • 1Laboratoire de Pharmacognosie, Unité d’Analyse Chimique et Physico-Chimique des Médicaments, Université Catholique de Louvain, Bruxelles, Belgium
  • 2CRCE, Histologie-Cytologie, Université de Liège, Liège, Belgium
  • 3Laboratoire de Spectrométrie de Masse, Université Catholique de Louvain, Louvain-la-Neuve, Belgium
  • 4Département de Physique Expérimentale, Université de Liège, Liège, Belgium
  • 5Département de Biologie Végétale, Faculté des Sciences et Techniques, Université Nationale du Bénin, Abomey-Calavy, Bénin
Further Information

Publication History

Received: March 8, 2002

Accepted: July 13, 2002

Publication Date:
26 November 2002 (online)

Abstract

Purification of a cytotoxic crude alkaloid extract of Cassytha filiformis led to the isolation of four known aporphine alkaloids: neolitsine, dicentrine, cassythine (= cassyfiline) and actinodaphnine. Their structures were determined by analysis of spectroscopic data. All isolated alkaloids were tested for their cytotoxic activities on cancer and non-cancer cell lines in vitro. Neolitsine was the most active against HeLa and 3T3 cells (IC50 :21.6 μM, and 21.4 μM, respectively). Cassythine and actinodaphnine showed the highest activity against Mel-5 (IC50 : 24.3 μM and 25.7 μM, respectively) and HL-60 (IC50 : 19.9 μM and 15.4 μM, respectively). This is the first report on the cytotoxic activity of C. filiformis extract and of neolitsine and cassythine. Furthermore, the complete NMR data of cassythine and actinodaphnine are given here for the first time.

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Caroline Stévigny

Laboratoire de pharmacognosie

Unité CHAM

UCL 72.30

Avenue E. Mounier 72

1200 Bruxelles

Belgium

Fax: + 32-2-764-73-63

Email: caroline.stevigny@cham.ucl.ac.be

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