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Acta Pharmaceutica Sinica ; (12): 869-873, 2010.
Artículo en Chino | WPRIM | ID: wpr-354562

RESUMEN

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.


Asunto(s)
Animales , Masculino , Ratones , Antidepresivos , Química , Farmacología , Clorhidrato de Duloxetina , Suspensión Trasera , Ratones Endogámicos ICR , Estructura Molecular , Antagonistas del Receptor de Serotonina 5-HT1 , Farmacología , Relación Estructura-Actividad , Natación , Tiofenos , Química , Farmacología
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