(1) Biopolymer Research Centre, CNR, c/o Department of Organic Chemistry, University of Padova, Via Marzolo 1, I-35131 Padova, Italy;(2) Department of Pharmacology, University of Padova, L.go Meneghetti 2, I-35131 Padova, Italy
Abstract:
Summary Dermorphin structure-activity relationships toward μ and δ opioid receptors were investigated using a series of synthetic
peptides, in which the aromatic residues at positions 1 or/and 3 of the N-terminal tetrapeptide analogue H-Tyr-d-Arg-Phe-β-Ala-NH2 were replaced by unnatural or constrained amino acids.