Literature DB >> 15740936

Synthesis of aryl semicarbazones as potential anticonvulsant agents.

P Yogeeswari1, D Sriram, V Veena, R Kavya, K Rakhra, J Vaigunda Ragavendran, S Mehta, R Thirumurugan, J P Stables.   

Abstract

A series of 4-ethoxyphenyl semicarbazones (1-10) have been synthesized using an appropriate synthetic route and characterized by elemental analyses and spectral data. The anticonvulsant activity of all the synthesized compounds was evaluated against maximal electroshock induced seizures (MES) and subcutaneous pentylenetetrazole (scPTZ) induced seizure models in mice. The neurotoxicity was assessed using the rotorod method. All the test compounds were administered at doses of 30, 100, and 300 mg/kg body weight and the anticonvulsant activity was noted at 0.5 and 4 h time intervals after the drug administration. Among the compounds tested, compounds except 3, 4 and 10 showed protection from seizures in both the animal models. Compounds 6 and 8 were found to increase gamma-aminobutyric acid (GABA) levels in the medulla oblongata region of the rat brain.

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Year:  2005        PMID: 15740936     DOI: 10.1016/j.biopha.2004.04.013

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


  3 in total

1.  Microwave-assisted synthesis, anticonvulsant activity and quantum mechanical modelling of N-(4-bromo-3-methylphenyl) semicarbazones.

Authors:  Mehta Shalini; Perumal Yogeeswari; Dharmarajan Sriram; Sridharan Induja
Journal:  J Zhejiang Univ Sci B       Date:  2007-01       Impact factor: 3.066

2.  Pyridine-4-carbaldehyde 4-phenylsemicarbazone.

Authors:  Rafael Mendoza-Meroño; Laura Menéndez-Taboada; Eva Fernández-Zapico; Santiago García-Granda
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-04-16

3.  Design, synthesis and anticonvulsant activity of some new 5,7-dibromoisatin semicarbazone derivatives.

Authors:  Dheeraj Kumar; Vijay Kumar Sharma; Rajeev Kumar; Tejendra Singh; Hariram Singh; Amar Deep Singh; R K Roy
Journal:  EXCLI J       Date:  2013-07-11       Impact factor: 4.068

  3 in total

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