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1.
Bioorg Med Chem ; 8(8): 2037-47, 2000 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-11003148

RESUMEN

In order to find novel nonsteroidal compounds possessing an inhibitory activity against delayed-type hypersensitivity (DTH) reactions, we conducted random screening using a picryl chloride (PC)-induced contact hypersensitivity reaction (CHR) in mice, and found compound 1 as a lead compound. Then we synthesized and evaluated an extensive series of 5-carboxamidouracil derivatives focused on both the uracil and the antioxidative moieties. Among them, we found that the hindered phenol moiety was necessary to exhibit the activities; especially, compounds 28a-28c having the partial structure of vitamin E were found to exert potent activities against the DTH reaction by both oral and topical administration. And compound 28c showed antioxidative activity against lipid peroxidation with an IC50 of 5.9 microM. Compound 28c (CX-659S) was chosen as a candidate drug for the treatment of cutaneous disorders such as atopic dermatitis and allergic contact dermatitis.


Asunto(s)
Antialérgicos/síntesis química , Antialérgicos/farmacología , Dermatitis Alérgica por Contacto/tratamiento farmacológico , Uracilo/síntesis química , Uracilo/farmacología , Animales , Antialérgicos/administración & dosificación , Antialérgicos/química , Antioxidantes/administración & dosificación , Antioxidantes/síntesis química , Antioxidantes/farmacología , Química Encefálica , Evaluación Preclínica de Medicamentos , Humanos , Peroxidación de Lípido/efectos de los fármacos , Masculino , Ratones , Ratones Endogámicos ICR , Estructura Molecular , Cloruro de Picrilo , Distribución Aleatoria , Ratas , Ratas Sprague-Dawley , Relación Estructura-Actividad , Uracilo/administración & dosificación , Uracilo/análogos & derivados
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