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Acta Pharmaceutica Sinica ; (12): 869-873, 2010.
Artigo em Chinês | WPRIM | ID: wpr-354562

RESUMO

In this paper, duloxetine was chosen as the lead compound. The pharmacophores with 5-HT(1A) antagonism activity were used to replace the naphthyl of duloxetine. A series of duloxetine derivatives had been designed and synthesized and whose structures were confirmed with elemental analysis, MS and H NMR. All synthesized compounds were tested by tail suspension test and forced swimming test in vivo. The test results revealed that most of the compounds have shown better activity than duloxetine at the same dosage. Some of them are worth to be studied further.


Assuntos
Animais , Masculino , Camundongos , Antidepressivos , Química , Farmacologia , Cloridrato de Duloxetina , Elevação dos Membros Posteriores , Camundongos Endogâmicos ICR , Estrutura Molecular , Antagonistas do Receptor 5-HT1 de Serotonina , Farmacologia , Relação Estrutura-Atividade , Natação , Tiofenos , Química , Farmacologia
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