Mai Hoang Linh, Grellier Philippe, Prost Elise, Lemoine Pascale, Poullain Cyril, Dumontet Vincent, Deguin Brigitte, Vo Thi Bach Hue, Michel Sylvie, Grougnet Raphaël
Laboratoire de Pharmacognosie, Université de Paris Descartes, Sorbonne Paris Cité, Faculté de Pharmacie de Paris, UMR-CNRS 8638 COMETE, 4 avenue de l'Observatoire, 75006 Paris, France.
Unité Molécules de Communication et Adaptation des Microorganismes (MCAM, UMR 7245), Muséum National d'Histoire Naturelle, CNRS, Sorbonne Universités, CP52, 57 rue Cuvier, 75005 Paris, France.
Phytochemistry. 2016 Feb;122:193-202. doi: 10.1016/j.phytochem.2015.11.001. Epub 2015 Nov 19.
A cycloartane gardurvilleic acid, three 3,4-seco-cycloartanes securvienol, secodienurvilleic acid, securvitriol, a 3,4;9,10-seco-cycloartane gardheptlactone, two dammaranes urvilone, urvilol, along with eight known cycloartanes and 3,4-seco-cycloartanes and four known dammaranes have been isolated from the bud exudate of Gardenia urvillei, an endemic tree to the New Caledonian dry forest. Two other dammarane derivatives have been obtained by semisynthesis. The structures of the original compounds were determined by spectroscopic methods and chemical correlations. In association with previously published data, the description of oxidized side-chains in position 17 are now available for two couples of diastereoisomers. Evaluation of anti-parasite activity and cytotoxicity has shown noticeable results for some of the isolated triterpenes.