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A new homologous series of anticonvulsants: phenyl alcohol amides. Synthesis and pharmacological evaluation.

作者信息

Meza-Toledo S E, Zenteno-García M T, Juárez-Carvajal E, Martínez-Muñoz D, Carvajal-Sandoval G

机构信息

Departamento de Bioquímica, Escuela Nacional de Ciencias Biológica, Instituto Politécnico Nacional (IPN), Mexico City, Mexico.

出版信息

Arzneimittelforschung. 1990 Dec;40(12):1289-91.

PMID:2095124
Abstract

The anticonvulsant activity of a homologous series of phenyl alcohol amides is described. (+-)-2-Hydroxy-2-phenylbutyramide (1), (+-)-3-hydroxy-3-phenylpentanamide (2) and (+-)-4-hydroxy-4-phenylhexanamide (3) were prepared and tested for their anticonvulsant profile and neurotoxicity. 1, 2 and 3 exhibited a broad profile of anticonvulsant activity and a similar significant activity in the seizures provoked by maximal electroshock, pentetrazol, 4-aminopyridine, bicuculline and thiosemicarbazide, but in the strychnine and picrotoxin tests, the protection was variable. The rotarod ataxia test was used to evaluate their neurotoxicity. In this test 2 possesses the lowest neurotoxicity.

摘要

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