ERDEM, Sinem AslanMITAINE-OFFER, Anne-ClaireMiyamoto, TomofumiKartal, MURATLACAILLE-DUBOIS, Marie-Aleth2020-10-292020-10-292015-02-01ERDEM S. A. , MITAINE-OFFER A., Miyamoto T., Kartal M., LACAILLE-DUBOIS M., -Triterpene saponins from Eryngium kotschyi-, PHYTOCHEMISTRY, cilt.110, ss.160-165, 2015http://hdl.handle.net/20.500.12645/26755Four new oleanane-type saponins 3-O-alpha-L-rhamnopyranosyl-(1 -> 4)-beta-D-glucuronopyranosyl-22-O-beta, beta-dimethylacryloylA1-barrigenol (1), 3-O-alpha-L-rhamnopyranosyl-(1 -> 4)-beta-D-glucuronopyranosyl-22-O-angeloylA1-barrigenol (2), 3-O-beta-D-glucopyranosyl-(1 -> 2)-[beta-D-glucopyranosyl-(1 -> 6)]-beta-D-glucopyranosyl-21,22,28-O-triacetyl-(3 beta,21 beta,22 alpha)-olean-12-en-16-one (3), and 3-O-beta-D-glucopyranosyl-(1 -> 2)-glucopyranosyl-22-O-beta-D-glucopyranosylsteganogenin (4), along with the known 3-O-beta-D-galactopyranosyl-(1 -> 2)-[alpha-L-arabinopyranosyl-(1 -> 3)]-beta-D-glucuronopyranosyl-22-O-angeloylA1-barrigenol and 3-O-alpha-L-rhamnopyranosyl-(1 -> 4)-beta-D-glucuronopyranosyloleanolic acid, were isolated from a methanol extract of the roots of Eryngium kotschyi by multiple chromatographic steps. Saponins 3 and 4 are unusual by the original structure of their aglycon. Compound 3 possessed an oleanane-type skeleton with a 21,22,28-triacetylation and a ketone function at the C-16 position. For compound 4, the 17,22-secooleanolic acid skeleton is rarely found in natural saponins. (C) 2014 Elsevier Ltd. All rights reserved.ArticleWOS:0003509213000178492150855310.1016/j.phytochem.2014.11.017