The MT2-selective melatonin receptor ligand UCM765 (N-(2-((3-methoxyphenyl)(phenyl)amino)ethyl)acetamide), showed interesting sleep inducing, analgesic and anxiolytic properties in rodents, but suffers from low water solubility and modest metabolic stability. To overcome these limitations, different strategies were investigated, including modification of metabolically liable sites, introduction of hydrophilic substituents and design of more basic derivatives. Thermodynamic solubility, microsomal stability and lipophilicity of new compounds were experimentally evaluated, together with their MT1 and MT2 binding affinities. Introduction of a m-hydroxymethyl substituent on the phenyl ring of UCM765 and replacement of the replacement of the N,N-diphenyl-amino scaffold with a N-methyl-N-phenyl-amino one led to highly soluble compounds with good microsomal stability and receptor binding affinity. Docking studies into the receptor crystal structure provided a rationale for their binding affinity. Pharmacokinetic characterization in rats highlighted higher plasma concentrations for the N-methyl-N-phenyl-amino derivative, consistent with its improved microsomal stability and makes this compound worthy of consideration for further pharmacological investigation.

N-(Anilinoethyl)amide Melatonergic Ligands with Improved Water Solubility and Metabolic Stability / Ferlenghi, F.; Mari, M.; Gobbi, G.; Elisi, G. M.; Mor, M.; Rivara, S.; Vacondio, F.; Bartolucci, S.; Bedini, A.; Fanini, F.; Spadoni, G.. - In: CHEMMEDCHEM. - ISSN 1860-7179. - 16:19(2021), pp. 3071-3082-3082. [10.1002/cmdc.202100405]

N-(Anilinoethyl)amide Melatonergic Ligands with Improved Water Solubility and Metabolic Stability

Ferlenghi F.;Elisi G. M.;Mor M.;Rivara S.;Vacondio F.;
2021

Abstract

The MT2-selective melatonin receptor ligand UCM765 (N-(2-((3-methoxyphenyl)(phenyl)amino)ethyl)acetamide), showed interesting sleep inducing, analgesic and anxiolytic properties in rodents, but suffers from low water solubility and modest metabolic stability. To overcome these limitations, different strategies were investigated, including modification of metabolically liable sites, introduction of hydrophilic substituents and design of more basic derivatives. Thermodynamic solubility, microsomal stability and lipophilicity of new compounds were experimentally evaluated, together with their MT1 and MT2 binding affinities. Introduction of a m-hydroxymethyl substituent on the phenyl ring of UCM765 and replacement of the replacement of the N,N-diphenyl-amino scaffold with a N-methyl-N-phenyl-amino one led to highly soluble compounds with good microsomal stability and receptor binding affinity. Docking studies into the receptor crystal structure provided a rationale for their binding affinity. Pharmacokinetic characterization in rats highlighted higher plasma concentrations for the N-methyl-N-phenyl-amino derivative, consistent with its improved microsomal stability and makes this compound worthy of consideration for further pharmacological investigation.
N-(Anilinoethyl)amide Melatonergic Ligands with Improved Water Solubility and Metabolic Stability / Ferlenghi, F.; Mari, M.; Gobbi, G.; Elisi, G. M.; Mor, M.; Rivara, S.; Vacondio, F.; Bartolucci, S.; Bedini, A.; Fanini, F.; Spadoni, G.. - In: CHEMMEDCHEM. - ISSN 1860-7179. - 16:19(2021), pp. 3071-3082-3082. [10.1002/cmdc.202100405]
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11381/2899746
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