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Acta Pharmaceutica Sinica ; (12): 994-1001, 2009.
Article in Chinese | WPRIM | ID: wpr-354606

ABSTRACT

A series of nitrogen-containing benzoheterocyclic derivatives were synthesized and tested for their antipsychotic activities. Their structures were confirmed by 1H NMR and HR-MS. Preliminary in vitro pharmacological trials showed that most of the target compounds have high affinity with D2 and 5-HT(2A) receptors. Among the tested compounds, 20 exhibited the highest affinity and D2 partial agonist activity. In vivo studies showed 20 has potent antipsychotic activities on apomorphine mice model, which is a chance to find a better precursor of D2 partial agonist for further optimization.


Subject(s)
Animals , Mice , Antipsychotic Agents , Pharmacology , Dopamine Agonists , Pharmacology , Drug Design , Isoquinolines , Pharmacology , Receptors, Dopamine D2 , Structure-Activity Relationship
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