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Aroylhydrazones constitute a promising class of 'metal-protein attenuating compounds' for the treatment of Alzheimer's disease: a proof-of-concept based on the study of the interactions between zinc(II) and pyridine-2-carboxaldehyde isonicotinoyl hydrazone
- Source :
- Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry. 23(8)
- Publication Year :
- 2018
-
Abstract
- With the increasing life expectancy of the world’s population, neurodegenerative diseases, such as Alzheimer’s disease (AD), will become a much more relevant public health issue. This fact, coupled with the lack of efficacy of the available treatments, has been driving research directed to the development of new drugs for this pathology. Metal-protein attenuating compounds (MPACs) constitute a promising class of agents with potential application on the treatment of neurodegenerative diseases, such as AD. Currently, most MPACs are based on 8-hydroxyquinoline. Recently, our research group has described the hybrid aroylhydrazone containing the 8-hydroxyquinoline group INHHQ as a promising MPAC. By studying the known structure-related ligand HPCIH, which does not contain the phenol moiety, as a simplified chemical model for INHHQ, we aimed to clarify the real impact of the aroylhydrazone group for the MPAC activity of a compound with potential anti-Alzheimer’s activity. The present work describes a detailed solution and solid-state study of the coordination of HPCIH with Zn2+ ions, as well as its in vitro binding-ability towards this metal in the presence of the Aβ(1–40) peptide. Similar to INHHQ, HPCIH is able to efficiently compete with Aβ(1–40) for Zn2+ ions, performing as expected for an MPAC. The similarity between the behaviors of both ligands is remarkable. Taken together, the data presented herein point to aroylhydrazones, such as the compounds HPCIH and the previously published INHHQ, as encouraging MPACs for the treatment of AD. Fil: Cukierman, Daphne S.. Pontifícia Universidade Católica do Rio de Janeiro; Brasil Fil: Accardo, Elio. Pontifícia Universidade Católica do Rio de Janeiro; Brasil Fil: Gomes, Rosana Garrido. Pontifícia Universidade Católica do Rio de Janeiro; Brasil Fil: De Falco, Anna. Pontifícia Universidade Católica do Rio de Janeiro; Brasil Fil: Miotto, Marco César. Universidad Nacional de Rosario; Argentina Fil: Freitas, Maria Clara Ramalho. Universidade Federal do Rio de Janeiro; Brasil Fil: Lanznaster, Mauricio. Universidade Federal Fluminense; Brasil Fil: Fernández, Claudio O.. Universidad Nacional de Rosario; Argentina Fil: Rey, Nicolás A.. Pontifícia Universidade Católica do Rio de Janeiro; Brasil
- Subjects :
- AROYLHYDRAZONES
Pyridines
Population
Hydrazone
Disease
Química Inorgánica y Nuclear
010402 general chemistry
Ligands
01 natural sciences
Biochemistry
Proof of Concept Study
Inorganic Chemistry
ZINC(II)
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
ALZHEIMER’S DISEASE
Alzheimer Disease
Coordination Complexes
Pyridine
Lack of efficacy
Moiety
education
Nootropic Agents
chemistry.chemical_classification
Aundefined PEPTIDE
education.field_of_study
Amyloid beta-Peptides
Molecular Structure
Chemistry
Ligand
Aβ peptide
Ciencias Químicas
Hydrazones
Combinatorial chemistry
Peptide Fragments
0104 chemical sciences
Zinc
MPAC
CIENCIAS NATURALES Y EXACTAS
030217 neurology & neurosurgery
Protein Binding
Subjects
Details
- ISSN :
- 14321327
- Volume :
- 23
- Issue :
- 8
- Database :
- OpenAIRE
- Journal :
- Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry
- Accession number :
- edsair.doi.dedup.....47698b2f5d0c15e20f360663e4def793