Titre :

Discovery of Compounds That Selectively Repress the Amyloidogenic Processing of the Amyloid Precursor Protein: Design, Synthesis and Pharmacological Evaluation of Diphenylpyrazoles.

Auteur(s) :

Mesangeau, Christophe [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Carato, Pascal [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Renault, Nicolas [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Coevoet, Mathilde [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Larchanché, Paul-Emmanuel [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Barczyk, Amélie [Auteur]
Institute for Translational Research in Inflammation - U 1286 [INFINITE]
Buee, Luc [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Sergeant, Nicolas [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Melnyk, Patricia [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172

Titre de la revue :

International Journal of Molecular Sciences

Nom court de la revue :

Int J Mol Sci

Numéro :

23

Date de publication :

2022-11-19

ISSN :

1422-0067

Mot(s)-clé(s) en anglais :

Alzheimer's disease
amyloid protein precursor
lysosome
autophagy
beta-secretase
pyrazole

Discipline(s) HAL :

Sciences du Vivant [q-bio]

Résumé en anglais : [en]

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 ...
Lire la suite >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 Aβ1–x peptide production, the increased stability of APP metabolites, and modulation of the ratio of autophagy markers. These screening parameters enabled us to select compounds as potent non-competitive β-secretase modulators, associated with various levels of lysosomotropic or autophagy modulatory activities. Structure–activity relationship analyses enabled us to define that (1) selectively reducing the production of Aβ1–x, and (2) little Aβx–40/42 modification together with (3) a decreased ratio of p62/(LC3-I/LC3-II) enabled the selection of non-competitive β-secretase modulators. Increased stability of CTFα and AICD precluded the selection of compounds with lysosomotropic activity whereas cell toxicity was associated with the sole p62 enhanced expression shown to be driven by the loss of nitrogen moieties. These SAR parameters are herein proposed with thresholds that enable the selection of potent anti-Alzheimer drugs for which further investigation is necessary to determine the basic mechanism underlying their mode of action.Lire moins >

Langue :

Anglais

Audience :

Internationale

Vulgarisation :

Non

Établissement(s) :

Université de Lille
Inserm
CHU Lille

Collections :

• Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
• Lille Neurosciences & Cognition (LilNCog) - U 1172

Date de dépôt :

2024-01-12T00:06:25Z
2024-02-28T09:57:59Z