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J Med Chem ; 24(5): 622-5, 1981 May.
Artigo em Inglês | MEDLINE | ID: mdl-7241521

RESUMO

The synthesis of three oligomeric derivatives of 4-isobutylphenyl-2-propionic acid (ibuprofen), namely, the monoester of tetraethylene glycol (I) and the diesters of poly(oxyethylene) samples having molecular weights of 1000 (+/- 50) and 2000 (+/- 150) (II and III), has been performed via the imidazolide method. The antiinflammatory activity of I-III, and of equivalent amounts of free drug, was determined in the carrageenan-induced rat paw edema assay at different times after oral administration and found to be considerably prolonged in the case of the three derivatives. The lowest molecular weight derivative (I) also had an enhanced initial activity with regard to 4-isobutylphenyl-2-propionic acid. These results were confirmed by measuring the plasma levels of 4-isobutylphenyl-2-propionic acid in rats at different times after oral administration.


Assuntos
Ibuprofeno/análogos & derivados , Animais , Anti-Inflamatórios/síntese química , Fenômenos Químicos , Química , Feminino , Ibuprofeno/síntese química , Ibuprofeno/farmacologia , Cinética , Dose Letal Mediana , Masculino , Camundongos , Ratos
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