Journal of Medicinal Chemistry · 2003 · 119 citations · 20 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryStructure-activity RelationshipsDrug-receptor InteractionsLigand BindingReceptor PharmacologyStructure-activity Relationship Analysis5-Hydroxytryptamine 3 Receptor AntagonistsAntihistamine PharmacologyHistamine Receptor AntagonismHistamine Receptor AntagonistsHistamine Receptor PharmacologyHistamine ReceptorsMembrane Receptor Activation
4-(Aminoalkoxy)benzylamines were prepared and screened for in vitro activity at the human histamine H(3) receptor. Some members of this series exhibited subnanomolar binding affinities. Analogues in which one nitrogen atom was replaced with a methine group showed greatly reduced binding affinities. Six members of this series were found to be antagonists in a cell-based model of human histamine H(3) receptor activation. One member of this series, 1-[4-(3-piperidin-1-ylpropoxy)benzyl]piperidine (7b), was found to be a selective and potent human H(3) receptor antagonist.
20
Xavier Ligneau, J Tardivel‐Lacombe, Florence Gbahou et al. · British Journal of Pharmacology · 2000 · 149 citations · Full text