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Yao Xue Xue Bao ; (12): 619-625, 2008.
Article in Chinese | WPRIM | ID: wpr-277786

ABSTRACT

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.


Subject(s)
Animals , Male , Mice , Rats , Antidepressive Agents , Pharmacology , Benzamidines , Pharmacology , Rats, Wistar , Serotonin , Selective Serotonin Reuptake Inhibitors , Pharmacology , Structure-Activity Relationship
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