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dc.contributor.authorRamos, E.-
dc.contributor.authorEgea, Javier-
dc.contributor.authorRios, C. de los-
dc.contributor.authorMarco-Contelles, José-
dc.contributor.authorRomero, A.-
dc.date.accessioned2017-07-27T09:56:21Z-
dc.date.available2017-07-27T09:56:21Z-
dc.date.issued2017-
dc.identifierdoi: 10.4155/fmc-2017-0014-
dc.identifierissn: 1756-8919-
dc.identifiere-issn: 1756-8927-
dc.identifier.citationFuture Medicinal Chemistry 9: 765- 780 (2017)-
dc.identifier.urihttp://hdl.handle.net/10261/153626-
dc.description.abstractMelatonin is an indoleamine produced mainly in the pineal gland. The natural decline of melatonin levels with aging strongly contributes to the development of neurodegenerative disorders. Pleiotropic actions displayed by melatonin prevent several processes involved in neurodegeneration such as neuroinflammation, oxidative stress, excitotoxicity and/or apoptosis. This review focuses on a number of melatonin hybrids resulting from the juxtaposition of tacrine, berberine, tamoxifen, curcumin, N,N-dibenzyl(N-methyl)amine, among others, with potential therapeutic effects for the treatment of neurodegenerative diseases.-
dc.publisherFuture Science-
dc.rightsclosedAccess-
dc.subjectMelatonin-
dc.subjectHybrid compounds-
dc.subjectMTDLs-
dc.subjectMultitarget-directed ligands-
dc.subjectNeurodegeneration-
dc.subjectAlzheimer's disease-
dc.subjectAntioxidant therapy-
dc.titleMelatonin as a versatile molecule to design novel multitarget hybrids against neurodegeneration-
dc.typeartículo-
dc.identifier.doi10.4155/fmc-2017-0014-
dc.relation.publisherversionhttp://dx.doi.org/10.4155/fmc-2017-0014-
dc.date.updated2017-07-27T09:56:21Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.relation.csic-
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