Drug Res (Stuttg) 2014; 64(01): 40-46
DOI: 10.1055/s-0033-1351316
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Design, Synthesis and Anticonvulsant Activity Evaluation of Novel 4-(4-Substitutedphenyl)-3-Methyl-1H-1,2,4-Triazol-5(4H)-Ones

Y. Zheng
1   College of Pharmacy, Yanbian University, Jilin, China
,
S.-B. Wang
1   College of Pharmacy, Yanbian University, Jilin, China
,
X. Cao
1   College of Pharmacy, Yanbian University, Jilin, China
,
D.-C. Liu
1   College of Pharmacy, Yanbian University, Jilin, China
,
B. Shu
1   College of Pharmacy, Yanbian University, Jilin, China
,
Z.-S. Quan
1   College of Pharmacy, Yanbian University, Jilin, China
› Institutsangaben
Weitere Informationen

Publikationsverlauf

received 06. Juni 2013

accepted 10. Juli 2013

Publikationsdatum:
21. August 2013 (online)

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Abstract

A series of novel 4-(4-substitutedphenyl)-3-methyl-1H-1,2,4-triazol-5(4H)-one derivatives were synthesized and screened for their anticonvulsant activities by the maximal electroshock test (MES) and their neurotoxicity was evaluated by the rotarod neurotoxicity test (TOX). In the MES test, compound 4-{4-[(3-fluorobenzyl)oxy]phenyl}-3-methyl-1H-1,2,4-triazol-5(4H)-one (4n) was found to possess better anticonvulsant activity and higher safety than marketed drugs Carbamazepine with an ED50 value of 25.5 mg/kg and protective index (PI) value>48.8. In addition, the potency of compound 4n against seizures induced by Pentylenetetrazole, 3-Mercaptopropionic acid, and Bicuculline suggested its broad spectrum activity, and the mechanisms of action including inhibition of voltage-gated ion channels and modulation of GABAergic activity might involve in its anticonvulsant activity.