CONFORMATIONAL RESTRICTION OF THE PHENYLALANINE RESIDUE IN A CYCLIC OPIOID PEPTIDE ANALOG - EFFECTS ON RECEPTOR SELECTIVITY AND STEREOSPECIFICITY

In an effort to determine the effect of side chain conformational restriction on opioid receptor selectivity, the cyclic phenylalanine analogues 2-aminoindan-2-carboxylic acid (Aic), 2-aminotetralin-2-carboxylic acid (Atc), and tetrahydroisoquinoline-3-carboxylic acid (Tic) were substituted for Phe in the potent cyclic opioid peptide analogue H-Tyr-D activated Orn-Phe-Glu-NH2, which lacks significant opioid receptor selectivity. Compounds were tested in mu- and delta-opioid receptor representative binding assays and bioassays in vitro. The analogue H-Tyr-D activated Orn-Aic-Glu-NH2 was found to be a potent agonist with high perference of mu-receptors over delta-receptors. Opening of the five-membered ring of Aic in the latter peptide, as achieved through substitution of C-alpha-methylphenylalanine or o-methylphenylalanine, resulted in only slightly selective compounds, indicating that the high mu-selectivity of the Aic analogue is exclusively the consequence of the imposed side chain conformational restriction. Both diastereoisomers of H-Tyr-D activated Orn-(D,L)-Atc-Glu-NH2 were highly mu-selective and, in contrast to the weak affinity observed with the D-Phe3 analogue as compared to the L-Phe3 analogue, both had similar potency. Thus, stereospecificity was lost as a consequence of side chain conformational restriction. Further structure-activity data obtained with analogues containing L- or D-homophenylalanine (Hfe) or 3-(1'-naphthyl)alanine (Nap) in place of Phe3 and consideration of geometric interrelationships between Nap and the L and D isomers of Atc, Hfe, and Phe led to the proposal that the D-Phe3 and the D-Atc3 analogue may have different modes of binding to the receptor. The very low potency observed with H-Tyr-D activated Orn-N-alpha-MePhe-Glu-NH2 (N-alpha-MePhe = N-alpha-methylphenylalanine) and H-Tyr-D activated Orn-Tic-Glu-NH2 indicated that N-alpha-alkylation at the 3-position is detrimental to activity.