Cytotoxic activity of proflavine diureas: synthesis, antitumor, evaluation and DNA binding properties of 1',1''-(acridin-3,6-diyl)-3',3''-dialkyldiureas

Bioorg Med Chem. 2008 Apr 1;16(7):3976-84. doi: 10.1016/j.bmc.2008.01.026. Epub 2008 Jan 19.

Abstract

The synthesis of novel 1',1''-(acridin-3,6-diyl)-3',3''-dialkyldiureas was reported. Their biological activity to inhibit cell proliferation was assessed by a MTT assay on two cell lines, HeLa and HCT-116, at micromolar concentration. 1',1''-(Acridin-3,6-diyl)-3',3''-dihexyldiurea hydrochloride was active on a HCT-116 cell line with an IC(50) value of 3.1 microM. The interaction of these compounds with calf thymus DNA was investigated by a variety of spectroscopic techniques including UV-vis, fluorescence and CD spectroscopy. From spectrofluorimetric titrations, binding constants for the DNA-drug complexes were determined (K=0.9-4.2x10(5) M(-1)). Antiproliferative activity of synthesized derivatives might be related to their intercalation into DNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acridines / chemistry*
  • Alkylation
  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / toxicity*
  • Apoptosis / drug effects
  • Cattle
  • Cell Line, Tumor
  • DNA / chemistry*
  • DNA / genetics
  • Humans
  • Molecular Structure
  • Photochemistry
  • Proflavine / chemistry*
  • Spectrophotometry
  • Structure-Activity Relationship
  • Titrimetry
  • Urea / chemical synthesis*
  • Urea / chemistry
  • Urea / toxicity*

Substances

  • Acridines
  • Antineoplastic Agents
  • Urea
  • DNA
  • Proflavine