Journal of Medicinal Chemistry · 1978 · 35 citations · 0 references
MedicineMedicinal ChemistryPharmacologyNeuropharmacologyPharmacodynamicsPsychopharmacologyLigand BindingReceptor PharmacologySerotonergic Pharmacology5-Hydroxytryptamine Receptor PharmacologyPharmacology Of Serotonergic AgentsResearch ArticlesSerotonin AgonistsSerotonin PharmacodynamicsSerotonin Receptor PharmacologySerotonin Receptor Subtypes
Hallucinogenic phenylalkylamine and N,N-dimethyltryptamine analogues are known to affect serotonergic systems both in vivo and in vitro. Using a rat stomach fundus model, the 5-HT receptor binding affinities of several of these analogues were determined and compared. The most behaviorally potent analogues examined, DOB, DOM, and 5-methoxy-N,N-dimethyltryptamine, were found to possess rather high affirmities (pA2 = 7.35, 7.12, and 7.08, respectively) for the 5-HT receptors of the model system.