Evidence map›Paper›PMID 39835556›Full record

ArticleMedicinal chemistry (Shariqah (United Arab Emirates))2025

Promising Anticancer Activity of Pyrazole Compounds against Glioblastoma Multiforme: Their Synthesis,

Kemal Alp Nalcı, Cihat Mete, Zeynep Demir, İshak Bildirici, Adnan Cetin

Abstract read
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In one paragraph

Article in Medicinal chemistry (Shariqah (United Arab Emirates)), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Kemal Alp NalcıDepartment of Pharmacology, Faculty of Pharmacy, Van Yüzüncü Yil University, Van, Türkiye.
Cihat MeteDepartment of Pharmaceutical Chemistry, Faculty of Education, Van Yüzüncü Yil University, Van, Türkiye.
Zeynep DemirDepartment of Pharmaceutical Chemistry, Faculty of Education, Van Yüzüncü Yil University, Van, Türkiye.
İshak BildiriciDepartment of Pharmaceutical Chemistry, Faculty of Education, Van Yüzüncü Yil University, Van, Türkiye.
Adnan CetinDepartment of Chemistry, Faculty of Education, Van Yüzüncü Yil University, Van, Türkiye.ORCID 0000-0003-4838-1503

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlioblastoma Multiforme (GBM), a highly aggressive and prevalent brain cancer with a higher incidence in males, has limited treatment success due to drug resistance, inadequate targeting and penetration of cancer cells, and an incomplete understanding of its molecular pathways. GBM is a highly aggressive brain cancer with limited treatment options. This study investigates the anticancer potential of synthesized pyrazole compounds against GBM cells.

methodsA series of pyrazole derivatives were synthesized and tested for their efficacy against GBM using MTT assays. Molecular docking studies were conducted to explore the binding interactions of these compounds with GBM receptors.

resultsCompounds 3 and 5 demonstrated significant anticancer activity, reducing cell viability more effectively than the control group. MTT assay results confirmed their potency. Molecular docking studies revealed strong binding interactions with GBM receptors, highlighting their potential as anticancer agents.

conclusionThe study evaluated the anticancer activity of synthesized compounds on human GBM cells, with compounds 3 and 5 showing the most promising results. Pyrazole 3 significantly reduced cell viability at high concentrations, while both pyrazoles 3 and 5 required higher doses to achieve substantial effects, as indicated by their IC

Indexed as

Antineoplastic AgentsBrain NeoplasmsGlioblastomaMolecular Docking SimulationPyrazolesCell Line, TumorCell ProliferationCell SurvivalDose-Response Relationship, DrugDrug Screening Assays, AntitumorHumansMolecular StructureStructure-Activity RelationshipAntineoplastic AgentsPyrazolesAnticancerbrain diseasesheterocyclicpharmacologic activitypyrazolespectroscopy.

Identifiers

PMID39835556

What Socratic holds

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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 Socratic graph.