Synthesis and structure-activity relationships of 1,5-diazaanthraquinones as antitumour compounds

Bioorg Med Chem Lett. 2004 Aug 2;14(15):3929-32. doi: 10.1016/j.bmcl.2004.05.055.

Abstract

1,5-Diazaanthraquinone derivatives were synthesized employing single and double hetero Diels-Alder strategies. Their in vitro antitumour activity was assayed using three cell lines. Some of these compounds, specially those bearing methyl or ethyl groups at the C-3,7 positions or chloro at C-4 and methyl at C-7, showed IC(50) values in the 10(-8)M range for human lung carcinoma and human melanoma, which makes them attractive candidates for further development as anticancer agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anthraquinones / chemical synthesis*
  • Anthraquinones / pharmacology*
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology
  • Aza Compounds / chemical synthesis*
  • Aza Compounds / pharmacology
  • Cell Division / drug effects
  • Cell Line, Tumor
  • Humans
  • Models, Molecular
  • Molecular Structure
  • Structure-Activity Relationship

Substances

  • Anthraquinones
  • Antineoplastic Agents
  • Aza Compounds