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Updated: Jul 16, 2026

A Straightforward Method for Glucosinolate Extraction and Analysis with High-pressure Liquid Chromatography (HPLC)
Published on: March 15, 2017
Structure of Triterpene-Sapogenins of Aesculus glabra1
E Aurada1, J Jurenitsch, W Kubelka
1Institut für Pharmakognosie der Universität Wien, Währinger Straße 25, A-1090 Wien.
Abstract:
After extraction of coarsely ground seeds of AESCULUS GLABRA Willd. with 80% methanol the saponin fraction was submitted to enzymatic and acid hydrolysis, giving qualitatively identical TLC-spectra of the sapogenins. For separation of the obtained sapogenins silica gel-columns with chloroform-methanol-water mixtures as mobile phases were employed. Five main components (genins G-A to G-E), identified as 21,22-diangeloyl-barringtogenol C, 21,22-diangeloyl-R (1)-barrigenol, 21-angeloyl-barringtogenol C, 22-angeloyl-R (1)-barrigenol and 21-angeloyl-R (1) barrigenol have been isolated. Structure elucidation was accomplished by (1)H-NMR and mass spectrometry of the genins, their acetates and several isopropyliden derivatives. The acid free sapogenins barringtogenol C and R (1) barrigenol (G-F and G-G) were found and identified by thin layer chromatography.
