Synthesis and anticonvulsant evaluation of some new 2,3,8-trisubstituted-4(3H)-quinazoline derivatives

Bioorg Med Chem Lett. 2012 Jan 1;22(1):327-33. doi: 10.1016/j.bmcl.2011.11.007. Epub 2011 Nov 16.

Abstract

A new series of 2,3,8-trisubstituted-4(3H)-quinazoline derivatives were synthesized, evaluated for their anticonvulsant activity against electrically (MES) and chemically (PTZ, picrotoxin and Strychnine) induced seizures and compared with the standard drugs methaqualone and sodium valproate. Compounds 3, 17 and 22 proved to be the most potent compounds of this series with relatively low neurotoxicity and low toxicity in the median lethal dose test as compared with the reference drugs. The obtained results showed that the most active compounds could be useful as a template for future design, modification and investigation to produce more active analogs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticonvulsants / pharmacology*
  • Chemistry, Pharmaceutical / methods*
  • Drug Design
  • Humans
  • Male
  • Methaqualone / pharmacology
  • Mice
  • Models, Chemical
  • Nervous System / drug effects
  • Quinazolines / pharmacology*
  • Seizures / drug therapy*
  • Valproic Acid / pharmacology

Substances

  • Anticonvulsants
  • Quinazolines
  • Valproic Acid
  • Methaqualone