Discovery of Compounds That Selectively Repress the Amyloidogenic Processing of the Amyloid Precursor Protein: Design, Synthesis and Pharmacological Evaluation of Diphenylpyrazoles.
Alzheimer’s disease
amyloid protein precursor
autophagy
lysosome
pyrazole
β-secretase
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
28 Oct 2022
28 Oct 2022
Historique:
received:
20
09
2022
revised:
14
10
2022
accepted:
18
10
2022
entrez:
11
11
2022
pubmed:
12
11
2022
medline:
15
11
2022
Statut:
epublish
Résumé
The rationale to define the biological and molecular parameters derived from structure-activity relationships (SAR) is mandatory for the lead selection of small drug compounds. Several series of small molecules have been synthesized based on a computer-assisted pharmacophore design derived from two series of compounds whose scaffold originates from chloroquine or amodiaquine. All compounds share similar biological activities. In vivo, Alzheimer's disease-related pathological lesions are reduced, consisting of amyloid deposition and neurofibrillary degeneration, which restore and reduce cognitive-associated impairments and neuroinflammation, respectively. Screening election was performed using a cell-based assay to measure the repression of Aβ
Identifiants
pubmed: 36361896
pii: ijms232113111
doi: 10.3390/ijms232113111
pmc: PMC9658513
pii:
doi:
Substances chimiques
Amyloid beta-Protein Precursor
0
Amyloid Precursor Protein Secretases
EC 3.4.-
Amyloid beta-Peptides
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Agence Nationale de la Recherche
ID : VIDALZ
Organisme : Association France Alzheimer
ID : 2020
Organisme : Agence Nationale de la Recherche
ID : Labex Distalz
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