Development of a model for the δ-opioid receptor pharmacophore. 4. Residue 3 dehydrophenylalanine analogues of Tyr-c[ D -Cys-Phe- D -Pen]OH (JOM-13) confirm required gauche orientation of aromatic side chain

We have previously proposed a model for the δ-opioid receptor binding conformation of the high affinity tetrapeptide Tyr-c[ D -Cys-Phe- D -Pen] OH (JOM-13) based on experimental and theoretical conformational analysis of this peptide and a correlation of conformational preferences of further conformationally restricted analogues of this tetrapeptide with their receptor binding affinities. A key element of this model is the requirement that the Phe 3 side chain exist in the x 1 = −60° conformation. Conformational calculations on the residue 3 dehydrophenylalanine analogues of JOM-13 suggest that while the dehydro( Z ) phenylalanine analogue can be superimposed easily with the proposed binding conformer of JOM-13, the dehydro( E )phenylalanine analogue cannot. These results lead to the prediction that the dehydro( Z )-phenylalanine analogue should display similar δ-receptor binding affinity as JOM-13 while the dehydro( E )phenylalanine analogue is expected to bind less avidly. Synthesis and subsequent opioid receptor binding analysis of the dehydrophenylalanine analogues of JOM-13 confirm these predictions, lending support to the δ-pharmacophore model. © 1996 John Wiley & Sons, Inc.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/37870/1/2_ftp.pd