Inhibitory effects of quassinoid derivatives on Epstein-Barr virus early antigen activation

Chem Pharm Bull (Tokyo). 1997 Apr;45(4):675-7. doi: 10.1248/cpb.45.675.

Abstract

Short-term in vitro assays for tumor promoters and antitumor promoters (Epstein-Barr virus activation test) were carried out for semisynthetic quassinoids (3-7), which were obtained by esterification of the C-15 OH group of deacetylated isobrucein-B (2). All the ester derivatives showed higher antitumor promoting activity than that of the potent compound 2. A compound containing a fluorinated aliphatic ester showed the highest potency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Viral / drug effects*
  • Antigens, Viral / immunology
  • Antineoplastic Agents, Phytogenic / chemistry*
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology
  • Glaucarubin / analogs & derivatives*
  • Glaucarubin / chemistry
  • Glaucarubin / pharmacology
  • Herpesvirus 4, Human
  • Quassins*
  • Tumor Cells, Cultured
  • Virus Activation / drug effects

Substances

  • Antigens, Viral
  • Antineoplastic Agents, Phytogenic
  • Antiviral Agents
  • Epstein-Barr virus early antigen
  • Quassins
  • isobrucein B
  • Glaucarubin