Evidence map›Paper›PMID 40810169›Full record

ArticleACS pharmacology & translational science2025

Discovery of Anticancer Indole-Based 4,5-Dihydroisoxazole Derivative with Selectivity toward Leukemia Cells.

Monika Majirská, Zuzana Kudličková, Natália Nosálová, Martin Kello, Radka Michalková, Danica Sabolová, Monika Tvrdoňová, Dávid Jáger, Martina Bago Pilátová, Martin Vojtek and 1 more

Abstract read
In one paragraph

Article in ACS pharmacology & translational science, 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. Review
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

11 authors.

Monika MajirskáDepartment of Pharmacology, Faculty of Medicine, Pavol Jozef Šafárik University in Košice, Košice 040 11, Slovakia.
Zuzana KudličkováInstitute of Chemistry, Faculty of Science, Pavol Jozef Šafárik University in Košice, Košice 041 80, Slovakia.
Natália NosálováSmall Animal Clinic, University of Veterinary Medicine and Pharmacy, Košice 041 81, Slovakia.
Martin KelloDepartment of Pharmacology, Faculty of Medicine, Pavol Jozef Šafárik University in Košice, Košice 040 11, Slovakia.ORCID https://orcid.org/0000-0002-2454-5799
Radka MichalkováDepartment of Pharmacology, Faculty of Medicine, Pavol Jozef Šafárik University in Košice, Košice 040 11, Slovakia.
Danica SabolováInstitute of Chemistry, Faculty of Science, Pavol Jozef Šafárik University in Košice, Košice 041 80, Slovakia.
Monika TvrdoňováInstitute of Chemistry, Faculty of Science, Pavol Jozef Šafárik University in Košice, Košice 041 80, Slovakia.ORCID https://orcid.org/0000-0002-9244-7242
Dávid JágerInstitute of Geotechnics, Slovak Academy of Sciences, Košice 040 01, Slovakia.
Martina Bago PilátováDepartment of Pharmacology, Faculty of Medicine, Pavol Jozef Šafárik University in Košice, Košice 040 11, Slovakia.
Martin VojtekLAQV/REQUIMTE, Laboratory of Pharmacology, Department of Drug Sciences, Faculty of Pharmacy, University of Porto, Porto 4050-313, Portugal.ORCID https://orcid.org/0000-0002-9257-7020
Carmen DinizLAQV/REQUIMTE, Laboratory of Pharmacology, Department of Drug Sciences, Faculty of Pharmacy, University of Porto, Porto 4050-313, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Isoxazole-derived compounds possess various bioactivities including anticancer, immunomodulatory, antimicrobial, anti-inflammatory, or antipsychotic effects with successful implementation in clinical practice. Treatment of hematological malignancies with isoxazole derivatives represents a promising area of research. The present study aimed to synthesize 11 novel 3,5-diaryl-4,5-dihydroisoxazole compounds and assess their antiproliferative effects using cell viability assay in a panel of nine cancer types including breast (MCF-7), colon (HCT-116), cervical (HeLa), lung (A549), ovarian cancer (A2780), glioblastoma (U87), hepatocellular carcinoma (HepG2), and leukemia (Jurkat and HL-60) cells as well as two noncancerous cell lines (Bj-5ta and MCF-10A). The most promising compound was further screened using flow cytometry, Western blot, fluorescence microscopy, and chemotaxis/migration cell assays. Compound (±)-3-[3-(4-bromophenyl)-4,5-dihydro-1,2-oxazol-5-yl]-1-methyl-1

Indexed as

cancerhematological malignancyisoxazolineleukemiaselectivity

Identifiers

PMID40810169
PMCPMC12340634

What OpenQuestion holds

Textmetadata
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.