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A novel series of cytotoxic iridoid glucosides derived from aucubin: design, synthesis and structure-activity
Vokatsoa C Rakotondramasy1, Christine Mouriès, Xavier Cachet
1Laboratoire de Pharmacognosie de l'Université Paris Descartes, U.M.R./C.N.R.S. n degrees 8638, Faculté des Sciences Pharmaceutiques et Biologiques, 4, Avenue de l'Observatoire, F-75006 Paris, France.
European Journal of Medicinal Chemistry
|March 16, 2010
Abstract:
Five new unsaturated iridolactones 3-7 related to natural cytotoxic oxylipins, Tei 9826, and iridolactone 2, were prepared by parallel synthesis from natural aucubin. It was found that perpivaloyl iridoid glucosides 2, 3, and 4 were markedly cytotoxic against both L1210 and KB-3-1 cell lines.

