| Literature DB >> 21353774 |
Douglas S Johnson1, Chung Choi, Lorraine K Fay, David A Favor, Joseph T Repine, Andrew D White, Hyacinth C Akunne, Lawrence Fitzgerald, Kim Nicholls, Bradley J Snyder, Steven Z Whetzel, Liming Zhang, Kevin A Serpa.
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).Entities:
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Year: 2011 PMID: 21353774 DOI: 10.1016/j.bmcl.2011.01.059
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823