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Bioorg Med Chem Lett ; 21(9): 2621-5, 2011 May 01.
Article in English | MEDLINE | ID: mdl-21353774

ABSTRACT

The synthesis and structure-activity relationship (SAR) of a novel series of aryl piperazine napthyridinone D(2) partial agonists is described. Our goal was to optimize the affinities for the D(2), 5-HT(2A) and 5-HT(1A) receptors, such that the D(2)/5-HT(2A) ratio was greater than 5 to ensure maximal occupancy of these receptors when the D(2) occupancy reached efficacious levels. This strategy led to identification of PF-00217830 (2) with robust inhibition of sLMA (MED=0.3mg/kg) and DOI-induced head twitches in rats (31% and 78% at 0.3 and 1mg/kg) with no catalepsy observed at the highest dose tested (10 mg/kg).


Subject(s)
Antipsychotic Agents/pharmacology , Naphthyridines/chemistry , Naphthyridines/pharmacology , Piperazines/chemistry , Piperazines/pharmacology , Receptors, Dopamine D2/agonists , Animals , Antipsychotic Agents/chemistry , Antipsychotic Agents/pharmacokinetics , Bipolar Disorder/drug therapy , Drug Discovery , Haplorhini , Male , Molecular Structure , Naphthyridines/pharmacokinetics , Piperazine , Piperazines/pharmacokinetics , Rats , Receptors, Dopamine D2/chemistry , Schizophrenia/drug therapy , Structure-Activity Relationship
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