Evidence map›Paper›PMID 40176684›Full record

ArticleChemical biology & drug design2025

The Development of Selective Chemical Probes for Serine Arginine Protein Kinase 3.

Danielle Hanke, Conall McCutcheon, Brent D G Page

Abstract read
In one paragraph

Article in Chemical biology & drug design, 2025. 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
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.

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

3 authors.

Danielle HankeFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
Conall McCutcheonFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
Brent D G PageFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.

Funding

Michael Smith Health Research BCNatural Sciences and Engineering Research Council of Canada
6 · The paper itself

Abstract

The serine arginine protein kinases (SRPKs) are a family of kinases whose irregular function is implicated in cancer and viral infections. While the roles of SRPK1 and SRPK2 in disease are well established, much less is known about SRPK3. There are several studies implicating SRPK3 in breast cancer, but the mechanism is still unknown. This work describes the first-reported SRPK3 chemical probes that show excellent selectivity over the other SRPKs. 1-(4-cyanophenyl)-3-phenylurea was identified as an initial hit for SRPK3 through a kinase screen. Subsequent rounds of in silico docking, medicinal chemistry optimization, and biochemical assays were performed to increase its potency and selectivity for SRPK3. Six top compounds were identified that displayed single digit micromolar IC

Indexed as

Protein Kinase InhibitorsProtein Serine-Threonine KinasesBreast NeoplasmsCell Line, TumorCell SurvivalFemaleHumansMolecular Docking SimulationStructure-Activity RelationshipProtein Kinase InhibitorsProtein Serine-Threonine KinasesSRPK3 protein, humanbreast cancerchemical probesmedicinal chemistryserine arginine protein kinasesSRPK3

Identifiers

PMID40176684
PMCPMC11966184

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.