Evidence map›Paper›PMID 32085971›Full record

ArticleBioorganic & medicinal chemistry letters2020

Development of 2-(4-pyridyl)-benzimidazoles as PKN2 chemical tools to probe cancer.

Fiona Scott, Angela M Fala, Lewis E Pennicott, Tristan D Reuillon, Katlin B Massirer, Jonathan M Elkins, Simon E Ward

Open access · hybridAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Illumination of understudied ciliary kinases.Frontiers in molecular biosciences · 2024
    Review
  5. Review
  6. Article
  7. 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

7 authors at 3 institutions in 2 countries.

Fiona ScottSussex Drug Discovery Centre, University of Sussex, Sussex House, Falmer, Brighton BN1 9RH, United Kingdom. Electronic address: f.scott@sussex.ac.uk.
Angela M FalaCentro de Química Medicinal (CQMED), Centro de Biologia Molecular e Engenharia Genética (CBMEG), Universidade Estadual de Campinas (UNICAMP), Campinas, SP 13083-875, Brazil; Structural Genomics Consortium, Departamento de Genética e Evolução, Instituto de Biologia, UNICAMP, Campinas, SP 13083-886, Brazil. Electronic address: angelafala@gmail.com.
Lewis E PennicottSussex Drug Discovery Centre, University of Sussex, Sussex House, Falmer, Brighton BN1 9RH, United Kingdom. Electronic address: l.e.pennicott@sussex.ac.uk.
Tristan D ReuillonSussex Drug Discovery Centre, University of Sussex, Sussex House, Falmer, Brighton BN1 9RH, United Kingdom. Electronic address: treuillo@its.jnj.com.
Katlin B MassirerCentro de Química Medicinal (CQMED), Centro de Biologia Molecular e Engenharia Genética (CBMEG), Universidade Estadual de Campinas (UNICAMP), Campinas, SP 13083-875, Brazil; Structural Genomics Consortium, Departamento de Genética e Evolução, Instituto de Biologia, UNICAMP, Campinas, SP 13083-886, Brazil. Electronic address: kmassire@unicamp.br.
Jonathan M ElkinsStructural Genomics Consortium, Nuffield Department of Medicine, University of Oxford, Oxford OX3 7DQ, United Kingdom. Electronic address: jon.elkins@sgc.ox.ac.uk.
Simon E WardSussex Drug Discovery Centre, University of Sussex, Sussex House, Falmer, Brighton BN1 9RH, United Kingdom; Medicines Discovery Institute, Cardiff University, Main Building, Park Place, Cardiff CF10 3AT, United Kingdom. Electronic address: wards10@cardiff.ac.uk.
University of Sussex · GBUniversidade Estadual de Campinas (UNICAMP) · BRUniversity of Oxford · GB

Funding

Wellcome TrustWellcome Trust 106169/ZZ14/Z
6 · The paper itself

Abstract

Kinases are signalling proteins which have proven to be successful targets for the treatment of a variety of diseases, predominantly in cancers. However, only a small proportion of kinases (<20%) have been investigated for their therapeutic viability, likely due to the lack of available chemical tools across the kinome. In this work we describe initial efforts in the development of a selective chemical tool for protein kinase N2 (PKN2), a relatively unexplored kinase of interest in several types of cancer. The most successful compound, 5, has a measured IC

Indexed as

Drug DevelopmentAntineoplastic AgentsBenzimidazolesCrystallography, X-RayDose-Response Relationship, DrugHumansModels, MolecularMolecular StructureNeoplasmsProtein Kinase CProtein Kinase InhibitorsStructure-Activity RelationshipAntineoplastic AgentsBenzimidazolesProtein Kinase CProtein Kinase Inhibitorsprotein kinase NAGC kinaseBenzimidazoleCancerChemical probeChemical toolHeart failureInflammationKinasesPKN2PRK2Protein kinase N2

Identifiers

PMID32085971
PMCPMC7078758
OpenAlexW3005560412

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.