Ochrolifuanines, alkaloid analogs of emetine and tubulosine: hemisynthesis and research on cytotoxic and antitumor properties

Seguin, E.; Trinh Minh Chau; Koch, M.; André, S.; Farjaudon, N.; Pareyre, C.; Tempête, C.; Robert-Géro, M.; Bourut, C.; Chenu, E.

Annales Pharmaceutiques Francaises 43(3): 301-310

1985


ISSN/ISBN: 0003-4509
PMID: 4083694
Document Number: 256357
Several ochrolifuanines, indole alkaloid analogs of emetine and tubulosine have been synthesized by PICTET-Spengler condensation between dihydrocorynantheal and various tryptamines. The study of the biological properties of these molecules (i.e.: determination of the cytotoxicity using the Allium test, effect on the growth of normal chick embryo fibroblasts, the transformation of these cells by Rous sarcoma virus and the effect on P 388 leukemia of mice) has established the expected cytotoxicity but has shown a lack of specificity towards tumor cells. The results are discussed in order to orient further synthesis to prepare more selective derivatives.

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