Opioid peptides. Partially modified retro-inverso dermorphin analogues. XIII.
Mauro Marastoni, Gianfranco Balboni, Roberto Tomatis, Severo Salvadori, Borea Pa, Licia Uccelli
Abstract
Mauro Marastoni, Gianfranco Balboni, Roberto Tomatis, Severo Salvadori, Borea Pa, Licia Uccelli
Abstract
We studied the effect of partial retro-inverso modification of a selected peptide bond of dermorphin (H-Tyr-D-Ala-Phe-Gly-Tyr-Pro-Ser-NH2) related peptides. The drastic loss of mu-receptor affinity following introduction of retro-inverso peptide bond between Phe1-D-Ala2 in the new peptide analogues, emphasized the importance of this backbone in the dermorphin peptides.
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We studied the effect of partial retro-inverso modification of a selected peptide bond of dermorphin (H-Tyr-D-Ala-Phe-Gly-Tyr-Pro-Ser-NH2) related peptides. The drastic loss of mu-receptor affinity following introduction of retro-inverso peptide bond between Phe1-D-Ala2 in the new peptide analogues, emphasized the importance of this backbone in the dermorphin peptides.
Key concepts: Dermorphin, Chemistry, Stereochemistry, Peptide, Peptide bond, Opioid peptide, Oligopeptide, Peptide synthesis