Literature DB >> 11345484

Anticonvulsant activity of p-chlorophenyl substituted arylsemicarbazones--the role of primary terminal amino group.

S N Pandeya1, V Mishra, I Ponnilavarasan, J P Stables.   

Abstract

A series of p-chlorophenyl substituted arylsemicarbazones were synthesized and evaluated for anticonvulsant activity. Most of the compounds provided significant protection against maximal electroshock-induced seizures (MES) at 100 mg/kg after 0.5 h and at 300 mg/kg after 4 h in both MES and pentetrazole-induced (PTZ) seizures. In the strychnine-induced seizures (scSTY), the majority of the compounds showed protection at 30 mg/kg. The compound 2 was active in both MES and PTZ tests. The study has shown that the terminal primary amino group is not necessary for anticonvulsant activity.

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Year:  2000        PMID: 11345484

Source DB:  PubMed          Journal:  Pol J Pharmacol        ISSN: 1230-6002


  3 in total

1.  Synthesis and evaluation of 4-substituted semicarbazones of levulinic acid for anticonvulsant activity.

Authors:  Navneet Aggarwal; Pradeep Mishra
Journal:  J Zhejiang Univ Sci B       Date:  2005-07       Impact factor: 3.066

2.  N-salicyloyltryptamine, a new anticonvulsant drug, acts on voltage-dependent Na+, Ca2+, and K+ ion channels.

Authors:  Démetrius Antonio Machado Araújo; Roberta Amaral Mafra; Andréia Laura Prates Rodrigues; Válter Miguel-Silva; Paulo Sérgio Lacerda Beirão; Reinaldo Nóbrega de Almeida; Lucindo Quintans; Maria Fátima Vanderlei de Souza; Jader Santos Cruz
Journal:  Br J Pharmacol       Date:  2003-12       Impact factor: 8.739

3.  Design and Synthesis of Some Novel 4-(4-substituted aryl) Semicarbazones as Anticonvulsant Agents.

Authors:  Anita Singh; C Pande; P Gahtori; S N Pandeya; J P Stables
Journal:  Indian J Pharm Sci       Date:  2010-05       Impact factor: 0.975

  3 in total

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