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This study reports the synthesis and biological evaluation of a series of new side-chain-to-side-chain cyclized endomorphin-2 (EM-2) and morphiceptin analogs of a general structure Tyr-c(Xaa-Phe-Phe-Yaa)NH 2 or Tyr-c(Xaa-Phe-d-Pro-Yaa)NH 2 , respectively, where Xaa and Yaa were l/d Asp or l/d Lys. Further modification of these analogs was achieved by introduction of 2′,6′-dimethyl-l-tyrosine...
In our previous paper we reported synthesis and biological activity of two cyclic analogs of endomorphin-2 (EM-2): Tyr-c(Lys-Phe-Phe-Asp)-NH 2 and Tyr-c(Asp-Phe-Phe-Lys)-NH 2 , achieved by making an amid bond between Lys and Asp side-chains. The first analog did not bind to the μ-opioid receptor, the affinity of the second one was very low. In the present study, we describe the synthesis...
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