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Synthesis and anticonvulsant evaluation of some new 6-[substituted-phenyl] thiazolo[3,2-b][l,2,4]triazole derivatives in mice
IJPR-Iranian Journal of Pharmaceutical Research. 2014; 13 (2): 459-469
em Inglês | IMEMR | ID: emr-142281
ABSTRACT
Epilepsy is the most frequent nearological affiction and afflicts 1% about of the worlds population. Currently there is an urgent need for the development of novel anticonvulsants with higher levels of potency and lower levels of toxicity. In this paper, a series of new 6-[substituted-phenyT] thiazolo[3,2-b][1.2.4]triazole derivatives were synthesized and tested for their anticonvulsant activities using the maximal electroshock [MES] and subcutaneous pentylenetetrazole [PTZ] screens, which are the most widely employed seizure models for early identification of candidate anticonvulsants. Their neurotoxicity was determined applying the rotarod test. In these compounds, 6-[4-fluorophenyl] thiazolo[3,2-b][l,2,4]triazole [3c] showed selective protection against the MES seizures with an ED[50] value of 49.1 mg/Kg and a TD[50] value of 94.1 mg/Kg, which provided compound 3c a protective index [PI = TD[50]/ED[50] of 1.9 in the MES test. 6-[4-Propoxyphenyl]thiazolo[3,2-b][l,2,4]triazole [5b] was found to be active in both models, i.e. MES test and PTZ test. In the PTZ screen, compound 5b gave an ED[50] of 63.4 mg/Kg and a TD[50] of 105.6 mg/Kg, resulting in a PI value of 1.7 which is higher than carbamazepine
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Índice: IMEMR (Mediterrâneo Oriental) Idioma: Inglês Revista: Iran. J. Pharm. Res. Ano de publicação: 2014

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Índice: IMEMR (Mediterrâneo Oriental) Idioma: Inglês Revista: Iran. J. Pharm. Res. Ano de publicação: 2014