Microwave assisted synthesis and docking study of N-(2-oxo-2-(4-oxo-2-substituted thiazolidin-3ylamino)ethyl)benzamide derivatives as anticonvulsant agents

Bioorg Med Chem Lett. 2014 Dec 15;24(24):5558-5562. doi: 10.1016/j.bmcl.2014.11.016. Epub 2014 Nov 11.

Abstract

Herewith, we report the design and synthesis of a series of N-(2-oxo-2((4-oxo-2-substituted thiazolidin-3yl)amino)ethyl) benzamide derivatives 7(a-j) under microwave irradiation, based on four component pharmacophoric model to get structural prerequisite indispensable for anticonvulsant activity. The synthesized derivatives were investigated in maximal electroshock seizure (MES), subcutaneous pentylenetetrazole (sc-PTZ) induced seizure and neurotoxicity screening. All the test compounds were administered at a dose of 30, 100 and 300 mg/kg body weight at the time interval of 0.5 h and 4 h. The compounds were also evaluated for behavioral activity and toxicity study. The compound 7 h was found to be most active in MES model. The anticonvulsant screening data shows that 65% of the compounds were found active against MES model when compared to 35% sc-PTZ model. The computational parameter such as docking study, logP determination and ADME prediction were performed to exploit the results.

Keywords: Anticonvulsant evaluation; Benzamide; Computational studies; Microwave irradiation; Thiazolidinone.

MeSH terms

  • Animals
  • Anticonvulsants / chemical synthesis*
  • Anticonvulsants / pharmacology
  • Anticonvulsants / therapeutic use
  • Benzamides / chemistry*
  • Benzamides / pharmacokinetics
  • Benzamides / therapeutic use
  • Binding Sites
  • Disease Models, Animal
  • Half-Life
  • Liver / pathology
  • Mice
  • Microwaves*
  • Molecular Docking Simulation
  • Motor Activity / drug effects
  • Protein Structure, Tertiary
  • Seizures / drug therapy
  • Sodium Channels / chemistry
  • Sodium Channels / metabolism
  • Thiazolidines / chemistry

Substances

  • Anticonvulsants
  • Benzamides
  • Sodium Channels
  • Thiazolidines