Planta Med 1993; 59(4): 293-295
DOI: 10.1055/s-2006-959684
Papers

© Georg Thieme Verlag Stuttgart · New York

Structure-Related Inhibiting Activity of Some Tobacco Cembranoids on the Prostaglandin Synthesis in vitro

Elisabeth Olsson1 , Anne Holth2 , Eva Kumlin2 , Lars Bohlin2 , Inger Wahlberg1
  • 1Reserca AB, S-118 84 Stockholm, Sweden
  • 2Department of Pharmacognosy, Biomedical Center, Uppsala University, Box 579, S-751 23 Uppsala, Sweden
Further Information

Publication History

1992

1992

Publication Date:
04 January 2007 (online)

Abstract

Structure-related inhibitory effects on the prostaglandin synthesis in vitro have been detected among eight diterpenoids of the cembrane class (1-8). The 4,6-diols 1 and 2 are the most active of the cembranoids studied with IC50 values of 0.36 and 0.39mM, respectively, as compared with an IC50 value of 1.4 for acetylsalicylic acid. Lower activities are found for cem-branoids having undergone oxidation of/at the 11,12 double bond (5-8), while the 4-hydroxy-6-oxocem-branoids 3 and 4 exhibit effects lower than those of 1 and 2 but higher than those of 5-8.