Journal of Medicinal Chemistry · 1996 · 20 citations · 10 references
MedicineMedicinal ChemistryPharmacologyNeuropharmacologyPharmacodynamicsPsychopharmacologyDrug ReceptorsDrug-receptor InteractionsLigand BindingReceptor PharmacologySerotonergic PharmacologyStructure-activity Relationship Analysis5-Hydroxytryptamine 1A Receptor Agonists5-Hydroxytryptamine Receptor PharmacologyBuspirone PharmacologyReceptor-ligand Binding AffinityReceptorsSerotonergic Drug DiscoverySerotonin AgonistsSerotonin Receptor Pharmacology
The synthesis and binding profile on 5-HT1A, 5-HT2, D-1, D-2, alpha 1, and alpha 2 receptors of the N-4 long-chain arylpiperazines 22-40 are reported, where an amino or amido function is inserted into the intermediate chain linked to the alpha position of the tetralin nucleus. Unlike the buspirone analogues, for the amido derivatives studied in this paper, the terminal amide function of long-chain piperazines is not important for 5-HT1A receptor affinity binding, and its removal yields high-affinity 5-HT1A receptor agents.
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Revathi K. Raghupathi, Laura Rydelek‐Fitzgerald, Milt Teitler et al. · Journal of Medicinal Chemistry · 1991 · 69 citations · Full text