Synthesis and antiproliferative properties of N3/8-disubstituted 3,8-diazabicyclo[3.2.1]octane analogues of 3,8-bis[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl-piperazine

Eur J Med Chem. 2007 Mar;42(3):293-306. doi: 10.1016/j.ejmech.2006.11.013. Epub 2006 Dec 5.

Abstract

A series of novel N(3/8)-disubstituted-3,8-diazabicyclo[3.2.1]octanes in order to improve the in vitro activity of the prototype 3,8-bis[2-(3,4,5-trimethoxyphenyl)pyridyl-4-yl)methylpiperazine (1) were synthesized and evaluated by assays of growth inhibition against several tumor cell lines. Compounds 2a,b,f and m demonstrated not only growth-inhibitory activities against leukemia cancer cells, but also fairly good activities against the growth of certain solid tumors. Among them, 2a is the most potent one with IC(50) values in the low micromolar range. Moreover, compound 2a has been selected for in vitro testing on MCF-7 cell to evaluate the mode of action of this lead compound.

MeSH terms

  • Alkylation
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects
  • Blotting, Western
  • Bridged Bicyclo Compounds, Heterocyclic / chemical synthesis*
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology*
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Cell Nucleus / drug effects
  • Cell Nucleus / ultrastructure
  • Cell Proliferation / drug effects
  • Coloring Agents
  • Diploidy
  • Electrophoresis, Polyacrylamide Gel
  • Humans
  • Indicators and Reagents
  • Microwaves
  • Piperazines / chemical synthesis*
  • Piperazines / pharmacology*
  • Propidium
  • Pyridines / chemical synthesis*
  • Pyridines / pharmacology*
  • Structure-Activity Relationship

Substances

  • 3,8-bis(2-(3,4,5-trimethoxyphenyl)pyridin-4-yl)methyl-piperazine
  • Antineoplastic Agents
  • Bridged Bicyclo Compounds, Heterocyclic
  • Coloring Agents
  • Indicators and Reagents
  • Piperazines
  • Pyridines
  • Propidium