Synthesis and biological evaluation of novel lipid A antagonists

Bioorg Med Chem. 2006 Jan 1;14(1):190-9. doi: 10.1016/j.bmc.2005.08.047. Epub 2005 Oct 3.

Abstract

A mimetic of Lipid A with a beta-N(OMe) glycosidic linkage, four linear C-14 hydrophobic chains and without phosphate groups has been prepared together with its beta-O-linked analogue. Both these molecules were active in inhibiting the inflammatory action of Escherichia coli lipid A on MT2 macrophages in a dose-dependent manner, while they were completely devoid of inflammatory activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbohydrate Sequence
  • Carbohydrates / chemical synthesis*
  • Carbohydrates / pharmacology*
  • Lipid A / antagonists & inhibitors*
  • Magnetic Resonance Spectroscopy
  • Molecular Mimicry
  • Molecular Sequence Data
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

  • Carbohydrates
  • Lipid A