A comparative study of antitumor activities and DNA cleavage on a class of dehydroabietylamine derivatives

Pharmazie. 2013 Nov;68(11):861-5.

Abstract

A series of novel dehydroabietylamine derivatives containing tricyclic diterpene structures were synthesized. The antitumor activities of these compounds against L02, Hey-1B and HepG2 cells were investigated. Significant activity was discovered forfourteen analogs. Meanwhile these compounds exhibit DNA cleavage activities on plasmid DNA (Escherichia coli), which depend on the Schiff base structure and the substituent of the aromatic moiety. Our findings present further information on the relationship between the chemical structure, biological function and DNA cleavage characteristics.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • DNA Cleavage / drug effects*
  • Diterpenes / chemical synthesis*
  • Diterpenes / pharmacology*
  • Drug Screening Assays, Antitumor
  • Humans
  • Indicators and Reagents
  • Iron / chemistry

Substances

  • Antineoplastic Agents
  • Diterpenes
  • Indicators and Reagents
  • Iron