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- Title
Synthesis and Evaluation of the Anticonvulsant Activities of 4-(2-(Alkylthio)benzo[d]oxazol-5-yl)-2,4-dihydro-3H-1,2,4-triazol-3-ones.
- Authors
Song, Ming-Xia; Wang, Zhen-Yuan; He, Shi-Hui; Yu, Sheng-Wang; Chen, Shi-Long; Guo, Dong-Fu; Zhao, Wen-Hao; Deng, Xian-Qing
- Abstract
In this study, a novel series of 4-(2-(alkylthio)benzo[<italic>d</italic>]oxazol-5-yl)-2,4-dihydro-3<italic>H</italic>-1,2,4-triazol-3-ones (<bold>4a</bold>–<bold>m</bold>) was designed and synthesized. The anticonvulsant activities of these compounds were evaluated by using the maximal electroshock seizure (MES) and subcutaneous pentylenetetrazole (scPTZ) seizure models in mice. The neurotoxicity of these compounds was evaluated using the rotarod neurotoxicity test. The majority of compounds showed anti-MES activities at 100 or 300 mg/kg. Compound <bold>4g</bold> was considered to be the most promising, based on its potency against MES- and PTZ-induced seizures with ED50 values of 23.7 and 18.9 mg/kg, respectively. The TD50 value of <bold>4g</bold> was 284.0 mg/kg, which resulted in a higher protective index (PI = TD50/ED50) value than that of carbamazepine and valproate. In an ELISA test, compound <bold>4g</bold> significantly increased the γ-aminobutyric acid (GABA) content in mouse brain. In addition, pretreatment with thiosemicarbazide (an inhibitor of the GABA synthesizing enzyme) significantly decreased the activity of <bold>4g</bold> in the MES model, which suggests that the mechanism through which compound <bold>4g</bold> elicits its anticonvulsive action is at least in part through increasing the GABA level in the brain.
- Subjects
TRIAZOLES; NEUROTOXICOLOGY; ANTICONVULSANTS; GABA; LABORATORY mice
- Publication
Molecules, 2018, Vol 23, Issue 4, p756
- ISSN
1420-3049
- Publication type
Article
- DOI
10.3390/molecules23040756