One-pot microwave assisted synthesis of new 2-alkoxycarbonylmethylene-4-oxo-1,5-benzo-, naphtho-, and pyridodiazepines and assessment of their cytogenetic activity

Eur J Med Chem. 2013 Sep:67:302-9. doi: 10.1016/j.ejmech.2013.06.028. Epub 2013 Jun 25.

Abstract

1,5-Benzo-, naphtho-, and pyridodiazepines 3 have been synthesized in excellent yields in one-step from the reaction of o-phenylenediamines with acetonedicarboxylates through microwave assisted acid catalysis. In order to ascertain their cytogenetic activity in vitro at doses equivalent to the per os doses of common 1,4-benzodiazepine drugs, Sister Chromatid Exchanges (SCEs) were employed, and for the determination of cytostaticity the Proliferation Rate Index (PRI) on lymphocytes of human whole blood cultures was estimated. It was found that benzodiazepines 3a, 3c, and 3e exhibit significant cytoprotection, but mild cytostatic effect (a statistically significant reduction of SCEs and a confined decrease of PRI values at similar concentrations). The most active compound was found to be 3e.

Keywords: 1,5-Benzodiazepines; Cytogenetic activity; Microwave irradiation; Proliferation Rate Index; Sister Chromatid Exchanges.

MeSH terms

  • Azepines / chemical synthesis
  • Azepines / chemistry
  • Azepines / pharmacology*
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Humans
  • Lymphocytes / cytology
  • Lymphocytes / drug effects*
  • Microwaves*
  • Molecular Structure
  • Pyridines / chemical synthesis
  • Pyridines / chemistry
  • Pyridines / pharmacology*
  • Sister Chromatid Exchange / drug effects*
  • Sister Chromatid Exchange / genetics
  • Structure-Activity Relationship

Substances

  • Azepines
  • Pyridines