| Literature DB >> 2898033 |
H Shimizu1, N Karai, A Hirose, T Tatsuno, H Tanaka, Y Kumasaka, M Nakamura.
Abstract
The propensity of SM-3997 to displace 3H-ligands was tested in vitro in a number of receptor-binding assays. SM-3997 possessed a high affinity towards 5-HT1A receptors, low affinity towards dopamine (D2) and 5-HT2 receptors, and no affinity towards benzodiazepine (BZ), GABA, 5-HT1B and adrenergic receptors. Moreover, SM-3997 facilitated neither 3H-flunitrazepam binding nor 3H-muscimol binding. These results suggest that the action of SM-3997 may be mediated via central 5-HT1A receptors but not the BZ-GABA receptor complex.Entities:
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Year: 1988 PMID: 2898033 DOI: 10.1254/jjp.46.311
Source DB: PubMed Journal: Jpn J Pharmacol ISSN: 0021-5198