Inhibitory effects of lapachol derivatives on epstein-barr virus activation

Bioorg Med Chem. 2003 Feb 20;11(4):483-8. doi: 10.1016/s0968-0896(02)00542-4.

Abstract

Sixteen derivatives (2-17) synthesized from the naphthoquinone lapachol (1), were tested for their inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activation induced by 12-O-tetradecanoylphorbol-13-acetate (TPA), as a test for potential cancer chemopreventive agents. They exhibited a variety of inhibitory activities from very high to moderate, which allow us to suggest structure-activity relationships. Ten of these derivatives are reported for the first time, their structures being thoroughly determined by spectroscopic methods.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acylation
  • Antigens, Viral / biosynthesis
  • Antigens, Viral / genetics
  • Antiviral Agents / chemical synthesis*
  • Antiviral Agents / pharmacology*
  • Cell Line
  • Cyclization
  • Herpesvirus 4, Human / drug effects*
  • Hydroxylation
  • Naphthoquinones / pharmacology*
  • Polycyclic Compounds / chemical synthesis
  • Polycyclic Compounds / pharmacology
  • Structure-Activity Relationship

Substances

  • Antigens, Viral
  • Antiviral Agents
  • Naphthoquinones
  • Polycyclic Compounds
  • lapachol