Hydrolysis and cytotoxic properties of osmium(II)/(III)-DMSO-azole complexes. Short communication

Chem Biodivers. 2008 Aug;5(8):1588-1593. doi: 10.1002/cbdv.200890146.

Abstract

The antiproliferative properties of the osmium(II) complexes cis,fac-[Os(II)Cl(2)(DMSO)(3)(L)] and trans,cis,cis-[Os(II)Cl(2)(DMSO)(2)(L)(2)] (L = 1H-pyrazole, 1H-imidazole) were studied in three human cancer cell lines, namely 41M (ovary), SK-BR-3 (breast), and SW480 (colon). Their activities were compared with those of osmium(III) and ruthenium(III) NAMI-A type complexes on HT-29 (colon) and SK-BR-3 cancer cell lines. While IC(50) values of all the Os(II) complexes were found to be >1000 microM in all cell lines, Os and Ru-NAMI-A type complexes showed remarkable antiproliferative activity. The marginal in vitro cytotoxicity of the Os(II) compounds is presumably attributed to their resistance to hydrolysis. However, the Os-NAMI-A complexes, which are also kinetically stable in aqueous solution, showed reasonable antiproliferative activity in vitro when compared with the analogous Ru compounds and with the Os(II)-DMSO-azole species, indicating that hydrolysis might be not a prerequisite for the antitumor activity of Os-NAMI-A type complexes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azoles / chemistry
  • Azoles / toxicity*
  • Cell Proliferation / drug effects
  • Dimethyl Sulfoxide / chemistry
  • Dimethyl Sulfoxide / toxicity*
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor
  • Humans
  • Hydrolysis / drug effects
  • Ligands
  • Molecular Conformation
  • Organometallic Compounds / chemical synthesis
  • Organometallic Compounds / chemistry*
  • Organometallic Compounds / pharmacology*
  • Osmium / chemistry
  • Osmium / toxicity*
  • Ruthenium / chemistry
  • Stereoisomerism
  • Structure-Activity Relationship
  • Tumor Cells, Cultured

Substances

  • Azoles
  • Ligands
  • Organometallic Compounds
  • Osmium
  • Ruthenium
  • Dimethyl Sulfoxide