
pmid: 23017884
A new construct for imitating a natural peptide ligand using a modified retro-inverso sequence is described. It is demonstrated through the synthesis of a peptidomimetic derived from the endogenous sequence of leucine enkephalin. The product was active at 400 nM and selective for μ-opioid receptors.
Molecular Structure, Polyamines, Receptors, Opioid, mu, Biological Availability, Humans, Peptidomimetics
Molecular Structure, Polyamines, Receptors, Opioid, mu, Biological Availability, Humans, Peptidomimetics
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