Evidence map›Paper›PMID 35628602›Full record

ArticleInternational journal of molecular sciences2022

The Small Molecule GAL-201 Efficiently Detoxifies Soluble Amyloid β Oligomers: New Approach towards Oral Disease-Modifying Treatment of Alzheimer's Disease.

Hermann Russ, Michele Mazzanti, Chris Parsons, Katrin Riemann, Alexander Gebauer, Gerhard Rammes

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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
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

6 authors at 2 institutions in 2 countries.

Hermann RussGalimedix Therapeutics Inc., 2704 Calvend Lane, Kensington, MD 20895, USA.
Michele MazzantiLaboratory of Cellular and Molecular Physiology, Department of Biosciences, University of Milano, Via Celoria 26, 20133 Milano, Italy.ORCID 0000-0002-1819-3811
Chris ParsonsGalimedix Therapeutics Inc., 2704 Calvend Lane, Kensington, MD 20895, USA.
Katrin RiemannDepartment of Anaesthesiology and Intensive Care Medicine, Technical University Munich, Ismaningerstr. 22, 81675 Munich, Germany.
Alexander GebauerGalimedix Therapeutics Inc., 2704 Calvend Lane, Kensington, MD 20895, USA.ORCID 0000-0002-8921-1829
Gerhard RammesDepartment of Anaesthesiology and Intensive Care Medicine, Technical University Munich, Ismaningerstr. 22, 81675 Munich, Germany.
Technical University of Munich · DEUniversity of Milan · IT

Funding

Galimedix The binding experiments, the pharmacokinetic studies, and the in vivo LTP studies have been financially supported by Merz Pharmaceuticals, Frankfurt.
6 · The paper itself

Abstract

Soluble amyloid β (Aβ) oligomers have been shown to be highly toxic to neurons and are considered to be a major cause of the neurodegeneration underlying Alzheimer's disease (AD). That makes soluble Aβ oligomers a promising drug target. In addition to eliminating these toxic species from the patients' brain with antibody-based drugs, a new class of drugs is emerging, namely Aβ aggregation inhibitors or modulators, which aim to stop the formation of toxic Aβ oligomers at the source. Here, pharmacological data of the novel Aβ aggregation modulator GAL-201 are presented. This small molecule (288.34 g/mol) exhibits high binding affinity to misfolded Aβ

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAnimalsHippocampusHumansLong-Term PotentiationNeuronal PlasticityRatsAmyloid beta-PeptidesAlzheimerbeta amyloidGAL-201hippocampusLTPneurodegenerative diseaseslicesoluble oligomerssynaptic plasticity

Identifiers

PMID35628602
PMCPMC9144469
OpenAlexW4281260236

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.