Summary
Acetophenone derivatives with a cortisone-like side chain have been investigated for their catalytic effect on the autoxydation of linolenic acid.ω-Hydroxy-acetophenone and the substitutedω-hydroxy-3,4-dimethoxyacetophenone are the substances with the simplest structure having a catalytic effect quantitatively and qualitatively similar to that of cortisone.
The significance of substituents in the ring for the catalytic activity of the side chain is discussed.
References
W. Schuler undR. Meier, Hoppe-Seylers Z.302, 236 (1955).
W. Schuler, unveröffentlichte Befunde.
F. Bernheim, M. K. Wilbur undC. B. Kenaston, Arch. Biochem. Biophys.38, 177 (1952).
A. Ottolenghi, F. Bernheim undK. M. Wilbur, Arch. Biochem. Biophys.56, 157 (1955).
C. W. Shuster, Proc. Soc. exp. Biol. Med. N. Y.90, 423 (1955).
W. D. Fisher andK. M. Wilbur, J. Elisha Mitchell Soc.70, 124 (1954).
K. M. Wilbur, G. B. Kenaston, N. Wolfson, A. Ottolenghi undM. E. Gaulden, Anat. Rec.120, 708 (1954).
W. Schuler undR. Meier, Arch. exp. Path. Pharmakol.228, 474 (1956).
W. Schuler undR. Meier, Helv. physiol. Acta15, 279 (1957).
Herrn Professor Dr.T. Reichstein danken wir auch an dieser Stelle bestens.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Schuler, W., Meier, R. Über einen Cortison-äquivalenten Katalysator der Autoxydation der Linolsäurein vitro. Experientia 14, 288–289 (1958). https://doi.org/10.1007/BF02167003
Published:
Issue Date:
DOI: https://doi.org/10.1007/BF02167003