Synthesis and in vitro antitumoral activity of new 3,5-dicyanopyridine derivatives

Bioorg Med Chem. 2007 Feb 15;15(4):1859-67. doi: 10.1016/j.bmc.2006.11.031. Epub 2006 Nov 19.

Abstract

A new series of 2-amino-4-aryl-6-dialkylamino-3,5-dicyanopyridines, 20-47, were synthesized in satisfactory overall yield, through a simple synthetic strategy using 3-amino-3-(dialkylamino)-propenenitriles 1 and 2 as key intermediates. 3,5-Dicyanopyridine derivatives 20-47 were evaluated for their in vitro anticancer activity toward cell lines of nine different types of human cancers. Some of the newly prepared compounds demonstrated inhibitory effects on the growth of a wide range of cancer cell lines generally at 10(-6) M level and in some cases at 10(-8) M concentration.

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Dose-Response Relationship, Drug
  • Humans
  • Pyridines / chemical synthesis*
  • Pyridines / pharmacology

Substances

  • Antineoplastic Agents
  • Pyridines