Synthesis of a resveratrol analogue with high ceramide-mediated proapoptotic activity on human breast cancer cells

J Med Chem. 2005 Nov 3;48(22):6783-6. doi: 10.1021/jm050528k.

Abstract

Resveratrol, a natural product with a stilbene structure, exerts profound proapoptotic activity in human cancer cells, by triggering the accumulation of ceramide, a bioactive sphingolipid. We studied the biological effects of seven methoxylated and/or naphthalene-based resveratrol analogues and compared these compounds with resveratrol with the objective to identify an analogue with higher ceramide-mediated proapoptotic activity relative to resveratrol. Here we show that the compound with three hydroxyls and a naphthalene ring is the most effective in triggering apoptosis coupled to the induction of endogenous ceramide in human cancer cells.

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Apoptosis*
  • Breast Neoplasms
  • Cell Line, Tumor
  • Ceramides / biosynthesis*
  • Drug Screening Assays, Antitumor
  • Female
  • Humans
  • Resveratrol
  • Stilbenes / chemical synthesis*
  • Stilbenes / chemistry
  • Stilbenes / pharmacology
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Ceramides
  • Stilbenes
  • Resveratrol