4 research outputs found
Substitution of the Side-Chain-Constrained Amino Acids β-Methyl-2‘,6‘-Dimethyl-4‘-Methoxytyrosine in Position 2 of a Bicyclic Oxytocin Analogue Provides Unique Insights into the Bioactive Topography of Oxytocin Antagonists
Cyclic enkephalin analogs with exceptional potency at peripheral .delta. opioid receptors
Cyclic Enkephalin Analogues with Exceptional Potency and Selectivity for δ-Opioid Receptors 1
Analogs of oxytocin containing a modified peptide bond Int
Analogs of deamino-oxytocin and deaminc-cxypressin containing a CH 1 -N H group instead of an amide bond between positions 8 and 9 were synthesized. All tested compounds exhibit significantly lowered biological activities