Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1397644 | European Journal of Medicinal Chemistry | 2011 | 5 Pages |
Bifunctional ligands containing an ester linkage between morphine and the δ-selective pharmacophore Dmt-Tic were synthesized, and their binding affinity and functional bioactivity at the μ, δ and κ opioid receptors determined. Bifunctional ligands containing or not a spacer of β-alanine between the two pharmacophores lose the μ agonism deriving from morphine becoming partial μ agonists 4 or μ antagonists 5. Partial κ agonism is evidenced only for compound 4. Finally, both compounds showed potent δ antagonism.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideResearch highlights► Morphine linked to the Dmt-Tic pharmacophore changes its pharmacological profile. μ Dmt-Tic-Morphine shows a antagonist activity comparable to naloxone. ► Dmt-Tic maintains its antagonist activity.