Synthesis and structure–activity relationship of novel aminotetralin derivatives with high μ selective opioid affinity

Synthesis and structure–activity relationship of novel aminotetralin derivatives with high μ selective opioid affinity Aminotetralins as narcotic antagonists. Synthesis and opiate-related activity of 1-phenyl-1-aminotetralin derivatives Aminothiazolomorphinans with Mixed κ and μ Opioid Activity Syntheses and Opioid Receptor Binding Affinities of 8-Amino-2,6-methano-3-benzazocines Highly selective .kappa. opioid analgesics. Synthesis and structure-activity relationships of novel N-[(2-aminocyclohexyl)aryl]acetamide and N-[(2-aminocyclohexyl)aryloxy]acetamide derivatives 1-Aryl-4-[(1-tetralinyl)alkyl]piperazines:  Alkylamido and Alkylamino Derivatives. Synthesis, 5-HT_1A Receptor Affinity, and Selectivity. 3 Selective Protection and Functionalization of Morphine:  Synthesis and Opioid Receptor Binding Properties of 3-Amino-3-desoxymorphine Derivatives^,1 Selective .kappa.-Opioid Agonists: Synthesis and Structure-Activity Relationships of Piperidines Incorporating an Oxo-Containing Acyl Group High Affinity and Selectivity on 5-HT1A Receptor of 1-Aryl-4-[(1-tetralin)alkyl]piperazines. 2 Synthesis and Pharmacology of a Novel κ Opioid Receptor (KOR) Agonist with a 1,3,5-Trioxazatriquinane Skeleton