Synthesis, cytotoxic evaluation, and DNA binding of novel thiazolo[5,4-b]quinoline derivatives

Bioorg Med Chem. 2008 Feb 1;16(3):1142-9. doi: 10.1016/j.bmc.2007.10.084. Epub 2007 Oct 30.

Abstract

A series of novel alkylamino and 9-anilinothiazolo[5,4-b]quinolines were synthesized as potential antitumoral agents. The in vitro cytotoxicity of these compounds was evaluated on several cell lines. The inclusion of electron-withdrawn/acceptor hydrogen-bond groups at position 3' of the anilino ring and the presence of an alkylamino chain on the tricyclic framework (regardless of its position) seem to be structural features relevant to cytotoxic activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Survival / drug effects
  • DNA / genetics*
  • Humans
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Quinolines / chemical synthesis*
  • Quinolines / chemistry
  • Quinolines / toxicity*
  • Structure-Activity Relationship
  • Thiazoles / chemistry*

Substances

  • Quinolines
  • Thiazoles
  • DNA