Structure–activity relationships of novel endomorphin-2 analogues with N–O turns induced by α-aminoxy acids

Abstract

Endomorphin-2 (H-Tyr-Pro-Phe-Phe-NH 2, EM-2) is a putative endogenous μ-opioid receptor ligand. To study the structure–activity relationship against its receptor, we introduced N–O turns into EM-2 and got the analogues with potent affinities for μ-opioid receptor. Our results indicated that N–O turn structures at the Pro 2-aminoxy-Phe 3 position of EM-2 analogues played important roles for their affinities. These novel analogues with N–O turns provided a new approach to develop potent analgesics related to EM-2.