Evidence map›Paper›PMID 31766108›Full record

ArticleMolecules (Basel, Switzerland)2019

[

Christian Lechner, Maren Flaßhoff, Hannes Falke, Lutz Preu, Nadége Loaëc, Laurent Meijer, Stefan Knapp, Apirat Chaikuad, Conrad Kunick

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Diabetic Kinome Inhibitors-A New Opportunity for β-Cells Restoration.International journal of molecular sciences · 2021
    Review
  6. GSK-3β, FYN, and DYRK1A: Master Regulators in Neurodegenerative Pathways.International journal of molecular sciences · 2021
    Review
  7. Review
  8. Article
  9. Article
  10. Article
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 4 institutions in 2 countries.

Christian LechnerInstitut für Medizinische und Pharmazeutische Chemie, Technische Universität Braunschweig, Beethovenstraße 55, 38106 Braunschweig, Germany.
Maren FlaßhoffInstitut für Medizinische und Pharmazeutische Chemie, Technische Universität Braunschweig, Beethovenstraße 55, 38106 Braunschweig, Germany.
Hannes FalkeInstitut für Medizinische und Pharmazeutische Chemie, Technische Universität Braunschweig, Beethovenstraße 55, 38106 Braunschweig, Germany.
Lutz PreuInstitut für Medizinische und Pharmazeutische Chemie, Technische Universität Braunschweig, Beethovenstraße 55, 38106 Braunschweig, Germany.
Nadége LoaëcFaculté de Médecine et des Sciences de la Santé UBO, 22 avenue Camille Desmoulins, 29200-Brest, France.
Laurent MeijerManRos Therapeutics & Perha Pharmaceuticals, Perharidy Research Center, 29680 Roscoff, France.ORCID 0000-0003-3511-4916
Stefan KnappInstitute for Pharmaceutical Chemistry and Buchmann Institute for Molecular Life Sciences, Johann Wolfgang Goethe University, Max-von-Laue-Str. 9, 60438 Frankfurt am Main, Germany.ORCID 0000-0001-5995-6494
Apirat ChaikuadInstitute for Pharmaceutical Chemistry and Buchmann Institute for Molecular Life Sciences, Johann Wolfgang Goethe University, Max-von-Laue-Str. 9, 60438 Frankfurt am Main, Germany.ORCID 0000-0003-1120-2209
Conrad KunickInstitut für Medizinische und Pharmazeutische Chemie, Technische Universität Braunschweig, Beethovenstraße 55, 38106 Braunschweig, Germany.ORCID 0000-0001-7041-5322
Technische Universität Braunschweig · DEGoethe University Frankfurt · DEManRos Therapeutics (France) · FRUniversité de Bretagne Occidentale · FR

Funding

Deutsche Forschungsgemeinschaft Ku-1371/10-1Deutsche Forschungsgemeinschaft SFB 1177European Commission FP7-KBBE-2012 grant (BlueGenics)Fondation Jérôme Lejeune unknownFonds Unique Interministériel TRIAD projectSCG unknown
6 · The paper itself

Abstract

Since hyperactivity of the protein kinase DYRK1A is linked to several neurodegenerative disorders, DYRK1A inhibitors have been suggested as potential therapeutics for Down syndrome and Alzheimer's disease. Most published inhibitors to date suffer from low selectivity against related kinases or from unfavorable physicochemical properties. In order to identify DYRK1A inhibitors with improved properties, a series of new chemicals based on [

Indexed as

Drug DesignDyrk KinasesHalogensHumansIndolesMolecular Docking SimulationMolecular Dynamics SimulationMolecular StructureProtein Kinase InhibitorsProtein Serine-Threonine KinasesProtein-Tyrosine KinasesSolubilitySpectrum AnalysisStructure-Activity RelationshipDyrk KinasesHalogensIndolesProtein Kinase InhibitorsProtein Serine-Threonine KinasesProtein-Tyrosine KinasesDYRK1Aindolemolecular dockingnephelometryprotein kinase inhibitorsolubilityX-ray structure analysis

Identifiers

PMID31766108
PMCPMC6891749
OpenAlexW2984098544

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.