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Acta Pharmaceutica Sinica ; (12): 619-625, 2008.
Artigo em Chinês | WPRIM | ID: wpr-277786

RESUMO

A series of biarylbenzamidine analogs were synthesized and tested for their biological activities of inhibiting the reuptake of 5-HT. All of them were new compounds, and their structures were confirmed by 1H NMR and HRMS. Preliminary in vitro pharmacological tests showed that all target compounds exhibited 5-HT reuptake inhibition activity. Among the tested compounds, 5i, 4a and 5m exhibited potent inhibitory activity against 5-HT reuptake in vitro. It is a chance to find a better precursor of SSRIs (selective serotonin reuptake inhibitors) for further optimization of compounds.


Assuntos
Animais , Masculino , Camundongos , Ratos , Antidepressivos , Farmacologia , Benzamidinas , Farmacologia , Ratos Wistar , Serotonina , Inibidores Seletivos de Recaptação de Serotonina , Farmacologia , Relação Estrutura-Atividade
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