The Structural Transformation of Gardenoside and Its Related Iridoid Compounds by Acid and β-Glucosidase
- 1 October 1987
- journal article
- research article
- Published by Georg Thieme Verlag KG in Planta Medica
- Vol. 53 (05) , 462-464
- https://doi.org/10.1055/s-2006-962773
Abstract
In the course of studies on the metabolism of iridoid compounds, three new compounds derived from 6α-hydroxygeniposide and 6β-hydroxygeniposide, obtained from gardenoside by the hydrochloric acid treatment, were isolated after the hydrolysis with β-glucosidase. The aglycone of 6β-hydroxygeniposide was elucidated as 6β-hydroxygenipin. On the other hand, the aglycones of 6α-hydroxygeniposide were identified as the mixture of stereoisomers, 6α-hydroxygenipin and 6α-hydroxy-1-epi-genipin.This publication has 4 references indexed in Scilit:
- Iridoids of garrya elliptica as plant growth inhibitorsPhytochemistry, 1984
- Studies on Iridoid-Related Compounds, II. The Structure and Antimicrobial Activity of Aglucones of Galioside and GardenosideJournal of Natural Products, 1983
- Iridoids in rothmannia globosaPhytochemistry, 1983
- Four iridoids from Randia canthioidesPhytochemistry, 1982