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Int. J. Mol. Sci. 2014, 15(9), 16114-16133; doi:10.3390/ijms150916114

Synthesis and Characterization of New Bivalent Agents as Melatonin- and Histamine H3-Ligands

1
Dipartimento di Farmacia, Università degli Studi di Parma, Parco Area delle Scienze 27/A, I-43124 Parma, Italy
2
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale, Università degli Studi di Milano, Via Vanvitelli 32, I-20129 Milano, Italy
3
Dipartimento di Scienze Biomolecolari, Università degli Studi di Urbino "Carlo Bo", Piazza Rinascimento 6, I-61029 Urbino, Italy
*
Author to whom correspondence should be addressed.
Received: 1 August 2014 / Revised: 3 September 2014 / Accepted: 4 September 2014 / Published: 12 September 2014
(This article belongs to the Special Issue Advances in the Research of Melatonin 2014)
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Abstract

Melatonin is an endogenous molecule involved in many pathophysiological processes. In addition to the control of circadian rhythms, its antioxidant and neuroprotective properties have been widely described. Thus far, different bivalent compounds composed by a melatonin molecule linked to another neuroprotective agent were synthesized and tested for their ability to block neurodegenerative processes in vitro and in vivo. To identify a novel class of potential neuroprotective compounds, we prepared a series of bivalent ligands, in which a prototypic melatonergic ligand is connected to an imidazole-based H3 receptor antagonist through a flexible linker. Four imidazolyl-alkyloxy-anilinoethylamide derivatives, characterized by linkers of different length, were synthesized and their binding affinity for human MT1, MT2 and H3 receptor subtypes was evaluated. Among the tested compounds, 14c and 14d, bearing a pentyl and a hexyl linker, respectively, were able to bind to all receptor subtypes at micromolar concentrations and represent the first bivalent melatonergic/histaminergic ligands reported so far. These preliminary results, based on binding affinity evaluation, pave the way for the future development of new dual-acting compounds targeting both melatonin and histamine receptors, which could represent promising therapeutic agents for the treatment of neurodegenerative pathologies. View Full-Text
Keywords: melatonin receptor; MT1; MT2; H3 antagonists; bivalent ligands melatonin receptor; MT1; MT2; H3 antagonists; bivalent ligands
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Pala, D.; Scalvini, L.; Lodola, A.; Mor, M.; Flammini, L.; Barocelli, E.; Lucini, V.; Scaglione, F.; Bartolucci, S.; Bedini, A.; Rivara, S.; Spadoni, G. Synthesis and Characterization of New Bivalent Agents as Melatonin- and Histamine H3-Ligands. Int. J. Mol. Sci. 2014, 15, 16114-16133.

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