Synthesis and in-vitro cytotoxic evaluation of novel pyridazin-4-one derivatives

Arch Pharm (Weinheim). 2010 May;343(5):310-3. doi: 10.1002/ardp.200900290.

Abstract

A new series of N-aryl-4-oxo-1,4-dihydro-pyridazine-3-carboxylic acids has been synthesized by condensation of aryldiazonium with 4-hydroxy-6-methyl-2-pyrone. Some of these compounds exhibited in-vitro cytotoxic activity with moderate to excellent growth inhibition against the murine P815 mastocytoma cell line. Compound 5b showed an important cytotoxic activity against cell line P815 (IC(50 )= 0.40 microg/mL).

MeSH terms

  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects*
  • Drug Screening Assays, Antitumor / methods
  • Mice
  • Molecular Structure
  • Pyridazines / chemical synthesis*
  • Pyridazines / pharmacology*
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Pyridazines