Glycolipid ester-type heterodimers from Ipomoea tyrianthina and their pharmacological activity

Bioorg Med Chem Lett. 2009 Aug 15;19(16):4652-6. doi: 10.1016/j.bmcl.2009.06.087. Epub 2009 Jun 25.

Abstract

Tyrianthins A (1) and B (2), two new partially acylated glycolipid ester-type heterodimers were isolated from Ipomoea tyrianthina. Scammonic acid A was determined as the glycosidic acid in both monomeric units. Tyrianthin A (1) (IC(50) 0.24+/-0.09 microM and E(max) 81.80+/-0.98%), and tyrianthin B (2) (IC(50) 0.14+/-0.08 microM and E(max) 87.68+/-0.72%) showed significant in vitro relaxant effect on aortic rat rings, in endothelium- and concentration-dependent manners. Also, these compounds were able to increase the release of GABA and glutamic acid in brain cortex, and displayed weak antimycobacterial activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antitubercular Agents / chemistry
  • Antitubercular Agents / isolation & purification
  • Antitubercular Agents / pharmacology
  • Dimerization
  • Glutamic Acid / metabolism
  • Glycolipids / chemistry*
  • Glycolipids / isolation & purification
  • Glycolipids / pharmacology
  • Ipomoea / chemistry*
  • Mice
  • Plant Roots / chemistry
  • Rats
  • Vasodilator Agents / chemistry*
  • Vasodilator Agents / isolation & purification
  • Vasodilator Agents / pharmacology
  • gamma-Aminobutyric Acid / metabolism

Substances

  • Antitubercular Agents
  • Glycolipids
  • Vasodilator Agents
  • tyrianthin A
  • tyrianthin B
  • Glutamic Acid
  • gamma-Aminobutyric Acid