Synthesis of some new coumarin incorporated thiazolyl semicarbazones as anticonvulsants

Acta Pol Pharm. 2009 Mar-Apr;66(2):161-7.

Abstract

Several heteroaryl semicarbazones were prepared by the reaction of heteroaryl hydrazine carboxamide with aryl aldehydes or ketones. The structures of the synthesized compounds were confirmed by spectral data and elemental analyses. Compounds were tested for anticonvulsant activity utilizing pentylenetetrazole-induced seizure (PTZ) and maximal electroshock seizure (MES) tests at 30, 100 and 300 mg/kg dose levels. Neurotoxicity of the compounds was also assessed at the same dose levels. Three compounds of the series, 6d, 6i and 6n, exhibited significant anticonvulsant activity at 30 mg/kg dose level comparable to the standard drug, phenytoin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticonvulsants / chemical synthesis*
  • Anticonvulsants / pharmacology*
  • Anticonvulsants / toxicity
  • Convulsants
  • Coumarins / chemical synthesis*
  • Coumarins / pharmacology*
  • Coumarins / toxicity
  • Electroshock
  • Female
  • Indicators and Reagents
  • Magnetic Resonance Spectroscopy
  • Male
  • Mice
  • Neurotoxicity Syndromes / psychology
  • Pentylenetetrazole
  • Seizures / chemically induced
  • Seizures / prevention & control
  • Semicarbazones / chemical synthesis*
  • Semicarbazones / pharmacology*
  • Semicarbazones / toxicity
  • Sodium Channels / drug effects
  • Spectrophotometry, Infrared
  • Thiazoles / chemical synthesis*
  • Thiazoles / pharmacology*
  • Thiazoles / toxicity

Substances

  • Anticonvulsants
  • Convulsants
  • Coumarins
  • Indicators and Reagents
  • Semicarbazones
  • Sodium Channels
  • Thiazoles
  • Pentylenetetrazole