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BY-NC-ND 3.0 license Open Access Published by De Gruyter June 2, 2014

Synthesis and Cytotoxic Activity of Methyl Glycyrrhetinate Esterified with Amino Acids

  • René Csuk EMAIL logo , Stefan Schwarz , Bianka Siewert , Ralph Kluge and Dieter Ströhl

Methyl glycyrrhetinate was esterified at position C3 of ring A using different amino acids. A short, unbranched chain of four carbon atoms with two amino groups in positions 2 and 4 was shown to be the most active compound of this series (IC50 = 0:8 M on liposarcoma Lipo cells). These compounds trigger apoptosis as shown by an acridine orange/ethidium bromide assay, trypan blue tests and DNA laddering experiments.

Graphical Abstract

 Synthesis and Cytotoxic Activity of Methyl Glycyrrhetinate Esterified with Amino Acids

Synthesis and Cytotoxic Activity of Methyl Glycyrrhetinate Esterified with Amino Acids

Received: 2012-4-19
Published Online: 2014-6-2
Published in Print: 2012-7-1

© 1946 – 2014: Verlag der Zeitschrift für Naturforschung

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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