Transformations in glycyrrhetinic acid: rearrangement of ring A
- 1 March 1966
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Pharmacy and Pharmacology
- Vol. 18 (3) , 168-174
- https://doi.org/10.1111/j.2042-7158.1966.tb07843.x
Abstract
Methyl 11-oxo-18 β-A-neo-oleana-3, 12-dien-30-oate and the corresponding 18α-isomer have been prepared and tested for anti-inflammatory and antidiuretic activity. Relative to methyl glycyrrhetinate, both kinds of activity and toxicity are reduced by the rearrangement. Features of interest in the nuclear magnetic resonance spectra of 18α- and 18 β-derivatives of glycyrrhetinic acid are recorded.This publication has 4 references indexed in Scilit:
- THE ANTI-INFLAMMATORY ACTIVITY OF GLYCYRRHETINIC ACID AND DERIVATIVESJournal of Pharmacy and Pharmacology, 1958
- Zur Frage des Mechanismus der Hemmung des Bindegewebswachstums durch CortisoneCellular and Molecular Life Sciences, 1950
- Zur Kenntnis der Triterpene. 138. Mitteilung. Über die Wasserabspaltung und Verseifungsgeschwindigkeit bei den epimeren Lupanolen-(2)Helvetica Chimica Acta, 1949
- A SIMPLE AND ACCURATE METHOD FOR THE DETERMINATION OF CHLORIDE IN BIOLOGICAL FLUIDSJournal of Biological Chemistry, 1941