Abstract
Herein we report attempts to optimize the pharmacological properties of 5-(2-hydroxyethoxy)-N-acetyltryptamine (5-HEAT), a melatonin receptor ligand previously described by us. Several 5-substituted and 2,5-disubstituted N-acyltryptamines were synthesized and evaluated in vitro for the human cloned MT1 and MT2 receptors. From this series of N-acyltryptamines the 2-bromo derivative (5c) retains the interesting efficacy profile of 5-HEAT and shows increased melatonin receptor affinities; it represents one of the first examples of a high-affinity MT, agonist/MT 2 antagonist. Some other full agonists for both melatonin receptors which exhibit similar or increased affinity relative to that of melatonin were obtained. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA.
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Spadoni, G., Bedini, A., Guidi, T., Tarzia, G., Lucini, V., Pannacci, M., & Fraschini, F. (2006). Towards the development of mixed MT1-agonist/MT 2-antagonist melatonin receptor ligands. ChemMedChem, 1(10), 1099–1105. https://doi.org/10.1002/cmdc.200600133
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