Synthesis and evaluation of amino-modified alpha-GalCer analogues

Org Lett. 2010 Jul 2;12(13):2928-31. doi: 10.1021/ol100934z.

Abstract

Alpha-GalCer analogues featuring a phytoceramide 3- and 4-amino group have been synthesized. A Mitsunobu reaction involving phthalimide was employed for the introduction of the amino groups at the 3- and 4-positions of suitable phytosphingosine-derived precursors. The influence of these modifications on the interaction with the T-cell receptor of NKT cells was investigated, as well as the capacity of the amino-modified analogues to induce a cytokine response after in vivo administration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Galactosylceramides / chemical synthesis*
  • Galactosylceramides / chemistry
  • Molecular Conformation
  • Stereoisomerism

Substances

  • Galactosylceramides