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Title

Donepezil + propargylamine + 8-hydroxyquinoline hybrids as new multifunctional metal-chelators, ChE and MAO inhibitors for the potential treatment of Alzheimer's disease

AuthorsWang, Li; Esteban, Gerard; Ojima, Masaki; Bautista-Aguilera, Óscar M.; Inokuchi, Tsutomu; Moraleda, Ignacio; Iriepa, Isabel; Samadi, Abdelouahid ; Youdim, Moussa B. H.; Romero, Alejandro ; Soriano, Elena ; Herrero, Raquel; Fernández Fernández, Ana Patricia ; Martínez-Murillo, Ricardo ; Marco-Contelles, José ; Unzeta, Mercedes
KeywordsDonepezil þ Propargylamine þ 8- Alzheimer’s disease
Hydroxyquinoline hybrids
Multifunctional drugs
Fe/Cu/Zn chelators
ChE and MAO inhibitors
In vivo scopolamine-induced long-term
memory deficit
Alzheimer’s disease
Issue Date2014
PublisherElsevier
CitationEuropean Journal of Medicinal Chemistry 80: 543- 561 (2014)
AbstractThe synthesis, biochemical evaluation, ADMET, toxicity and molecular modeling of novel multi-target-directed Donepezil + Propargylamine + 8-Hydroxyquinoline (DPH) hybrids 1-7 for the potential prevention and treatment of Alzheimer's disease is described. The most interesting derivative was racemic α-aminotrile4-(1-benzylpiperidin-4-yl)-2-(((8-hydroxyquinolin-5-yl) methyl)(prop-2-yn-1-yl)amino) butanenitrile (DPH6) [MAO A (IC50 = 6.2 ± 0.7 μM; MAO B (IC50 = 10.2 ± 0.9 μM); AChE (IC50 = 1.8 ± 0.1 μM); BuChE (IC50 = 1.6 ± 0.25 μM)], an irreversible MAO A/B inhibitor and mixed-type AChE inhibitor with metal-chelating properties. According to docking studies, both DPH6 enantiomers interact simultaneously with the catalytic and peripheral site of EeAChE through a linker of appropriate length, supporting the observed mixed-type AChE inhibition. Both enantiomers exhibited a relatively similar position of both hydroxyquinoline and benzyl moieties with the rest of the molecule easily accommodated in the relatively large cavity of MAO A. For MAO B, the quinoline system was hosted at the cavity entrance whereas for MAO A this system occupied the substrate cavity. In this disposition the quinoline moiety interacted directly with the FAD aromatic ring. Very similar binding affinity values were also observed for both enantiomers with ChE and MAO enzymes. DPH derivatives exhibited moderate to good ADMET properties and brain penetration capacity for CNS activity. DPH6 was less toxic than donepezil at high concentrations; while at low concentrations both displayed a similar cell viability profile. Finally, in a passive avoidance task, the antiamnesic effect of DPH6 was tested on mice with experimentally induced amnesia. DPH6 was capable to significantly decrease scopolamine-induced learning deficits in healthy adult mice. © 2014 Elsevier Masson SAS. All rights reserved.
URIhttp://hdl.handle.net/10261/98829
DOI10.1016/j.ejmech.2014.04.078
Identifiersdoi: 10.1016/j.ejmech.2014.04.078
issn: 0223-5234
e-issn: 1768-3254
Appears in Collections:(IQOG) Artículos
(IC) Artículos
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