Evidence map›Paper›PMID 36361896›Full record

ArticleInternational journal of molecular sciences2022

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

Christophe Mesangeau, Pascal Carato, Nicolas Renault, Mathilde Coevoet, Paul-Emmanuel Larchanché, Amélie Barczyk, Luc Buée, Nicolas Sergeant, Patricia Melnyk

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 80% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Christophe MesangeauU1172-LilNCog-Lille Neurosciences & Cognition, Univ. Lille, Inserm, CHU Lille, F-59000 Lille, France.
Pascal CaratoU1172-LilNCog-Lille Neurosciences & Cognition, Univ. Lille, Inserm, CHU Lille, F-59000 Lille, France.ORCID 0000-0002-8893-5155
Nicolas RenaultU1286-INFINITE-Institute for Translational Research in Inflammation, Univ. Lille, Inserm, CHU Lille, F-59000 Lille, France.ORCID 0000-0002-4859-1212
Mathilde CoevoetU1172-LilNCog-Lille Neurosciences & Cognition, Univ. Lille, Inserm, CHU Lille, F-59000 Lille, France.ORCID 0000-0001-7529-6676
Paul-Emmanuel LarchanchéU1172-LilNCog-Lille Neurosciences & Cognition, Univ. Lille, Inserm, CHU Lille, F-59000 Lille, France.
Amélie BarczykU1286-INFINITE-Institute for Translational Research in Inflammation, Univ. Lille, Inserm, CHU Lille, F-59000 Lille, France.
Luc BuéeU1172-LilNCog-Lille Neurosciences & Cognition, Univ. Lille, Inserm, CHU Lille, F-59000 Lille, France.ORCID 0000-0002-6261-4230
Nicolas SergeantU1172-LilNCog-Lille Neurosciences & Cognition, Univ. Lille, Inserm, CHU Lille, F-59000 Lille, France.ORCID 0000-0003-1448-124X
Patricia MelnykU1172-LilNCog-Lille Neurosciences & Cognition, Univ. Lille, Inserm, CHU Lille, F-59000 Lille, France.ORCID 0000-0002-9555-3446
Inserm · FR

Funding

Agence Nationale de la Recherche Labex DistalzAgence Nationale de la Recherche VIDALZAssociation France Alzheimer 2020
6 · The paper itself

Abstract

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

Indexed as

Alzheimer DiseaseAmyloid beta-Protein PrecursorAmyloid beta-PeptidesAmyloid Precursor Protein SecretasesHumansStructure-Activity RelationshipAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAmyloid Precursor Protein SecretasesAlzheimer’s diseaseamyloid protein precursorautophagylysosomepyrazoleβ-secretase

Identifiers

PMID36361896
PMCPMC9658513
OpenAlexW4307947553

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.