Imidazopyridine-fused [1,3]-diazepinones: synthesis and antiproliferative activity

Eur J Med Chem. 2014 Mar 21:75:382-90. doi: 10.1016/j.ejmech.2014.01.044. Epub 2014 Jan 30.

Abstract

A series of 15 pyrido-imidazo-1,3-diazepin-5-ones and pyrido-1,3-diazepine-2,5-diones were synthesized and their anticancer activities were evaluated. Among tested compounds on a cell lines panel, compound 6a presents the best growth inhibition activity on 21 cell lines with a cytotoxic effect on MDA-MB-435 melanoma cells. This compound led to deep cell morphological changes and revealed to be an inhibitor of the Hepatocyte progenitor kinase-like kinase (HGK), which is known to be implicated in the migration, adhesion and invasion of various tumor cells.

Keywords: Antitumor activity; Diazepinones; HGK inhibitors; Imidazo[1,2-a]pyridine; Polyfused heterocycles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacology*
  • Azepines / chemistry*
  • Azepines / pharmacology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Drug Screening Assays, Antitumor
  • Humans
  • Neoplasms / drug therapy
  • Neoplasms / enzymology
  • Pyridines / chemistry*
  • Pyridines / pharmacology*

Substances

  • Antineoplastic Agents
  • Azepines
  • Pyridines