Evidence map›Paper›PMID 40626906›Full record

ArticleChemMedChem2025

Development of Novel Anticancer Pyrazolopyrimidinones Targeting Glioblastoma.

Kate Byrne, Natalia Bednarz, Ciara McEvoy, John C Stephens, James F Curtin, Gemma K Kinsella

Abstract read
In one paragraph

Article in ChemMedChem, 2025. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Access to Pyrazolo[1,5-Organic letters · 2026
    Article
  3. Article
  4. 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

6 authors.

Kate ByrneSchool of Food Science and Environmental Health, Technological University Dublin, Grangegorman Lower, Dublin 7, Dublin, D07 ADY7, Ireland.
Natalia BednarzSchool of Food Science and Environmental Health, Technological University Dublin, Grangegorman Lower, Dublin 7, Dublin, D07 ADY7, Ireland.
Ciara McEvoySchool of Food Science and Environmental Health, Technological University Dublin, Grangegorman Lower, Dublin 7, Dublin, D07 ADY7, Ireland.
John C StephensDepartment of Chemistry, Maynooth University, Maynooth, W23 F2H6, Ireland.
James F CurtinSchool of Food Science and Environmental Health, Technological University Dublin, Grangegorman Lower, Dublin 7, Dublin, D07 ADY7, Ireland.
Gemma K KinsellaSchool of Food Science and Environmental Health, Technological University Dublin, Grangegorman Lower, Dublin 7, Dublin, D07 ADY7, Ireland.ORCID https://orcid.org/0000-0002-6329-5841

Funding

Fiosraigh Dean of Graduate Research School Award PB04280Science Foundation Ireland 21/FFP-A/9189
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most common and aggressive malignant grade IV brain tumor and is one of the most difficult types of brain cancer to treat with a high incidence of resistance to traditionally used chemotherapeutics. Pyrazolopyrimidinones are fused nitrogen-containing heterocyclic systems which are a scaffold in several bioactive drugs and drug candidates. Here, a structure-activity relationship (SAR) study was performed where 23 substituted pyrazolo[1,5-α]pyrimidinones were screened for cytotoxicity against the GBM U-251 MG cell line and the noncancerous embryonic kidney HEK293 cell line to assess their potential as antiGBM agents capable of selectivity for cancer cells. Through analog synthesis of preliminary HIT compounds with varied structural substituents, a lead compound, 22, has been identified, which proved capable of inducing significant GBM cell death while having a marginal cytotoxicity against the noncancerous cells. The mode of cell death studies suggested that the structurally varied HIT compounds induced cell death through differential mechanisms including cell membrane permeabilization and mitochondria membrane depolarization-dependent mechanisms such as necrosis or apoptosis. The results highlight the potential of pyrazolo[1,5-α]pyrimidinones derivatives as a novel anti-GBM therapy, capable of selectively killing cancer cells. Furthermore, pyrazolo[1,5-α]pyrimidinones provide a scaffold for further development of selective GBM therapies.

Indexed as

Antineoplastic AgentsDrug DevelopmentGlioblastomaPyrazolesPyrimidinonesApoptosisCell Line, TumorCell ProliferationDose-Response Relationship, DrugDrug Screening Assays, AntitumorHEK293 CellsHumansMolecular StructureStructure-Activity RelationshipAntineoplastic AgentsPyrazolesPyrimidinonescancerglioblastomapyrazolo[1,5‐α]pyrimidinonesstructure‐activity relationships

Identifiers

PMID40626906
PMCPMC12530846

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Registered trials

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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.