Structure-activity relationship of alpha-galactosylceramides against B16-bearing mice

J Med Chem. 1995 Jun 9;38(12):2176-87. doi: 10.1021/jm00012a018.

Abstract

Agelasphin-9b, (2S,3S,4R)-1-O-(alpha-D-galactopyranosyl)-16-methyl-2- [N-((R)-2- hydroxytetracosanoyl)-amino]- 1,3,4-heptadecanetriol, is a potent antitumor agent isolated from the marine sponge Agelas mauritianus. Various analogues of agelasphin-9b (a lead compound) were synthesized, and the relationship between their structures and biological activities was examined using several assay systems. From the results, KRN7000, (2S,3S,4R)-1-O-(alpha-D- galactopyranosyl)-2-(N-hexacosanoylamino)-1,3,4-octadecanetriol , was selected as a candidate for clinical application.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Cell Division / drug effects
  • Drug Screening Assays, Antitumor
  • Female
  • Fetal Blood
  • Galactosylceramides / chemistry
  • Galactosylceramides / pharmacology*
  • Humans
  • Lymphocytes / cytology
  • Lymphocytes / drug effects
  • Melanoma, Experimental / pathology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Porifera / chemistry
  • Spleen / cytology
  • Spleen / drug effects
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Galactosylceramides