Evidence map›Paper›PMID 32328961›Full record

ArticleMolecular diversity2021

Design, synthesis, and anticancer activity of novel 4-thiazolidinone-phenylaminopyrimidine hybrids.

Aslı Türe, Mustafa Ergül, Merve Ergül, Ahmet Altun, İlkay Küçükgüzel

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular diversity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Diverse Biological Activity of Pyrimidine Derivatives: A Review.Current drug discovery technologies · 2026
    Review
  4. Article
  5. A Review on Medicinal Approaches of Novel Imatinib Derivatives.Current topics in medicinal chemistry · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 4-Thiazolidinone-Bearing Hybrid Molecules in Anticancer Drug Design.International journal of molecular sciences · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. 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

5 authors at 2 institutions in 1 country.

Aslı TüreDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Marmara University, P.O. Box: 34668, Istanbul, Turkey.ORCID http://orcid.org/0000-0003-3422-7425
Mustafa ErgülDepartment of Biochemistry, Faculty of Pharmacy, Sivas Cumhuriyet University, Sivas, Turkey.ORCID http://orcid.org/0000-0003-4303-2996
Merve ErgülDepartment of Pharmacology, Faculty of Pharmacy, Sivas Cumhuriyet University, Sivas, Turkey.ORCID http://orcid.org/0000-0003-4661-8087
Ahmet AltunDepartment of Medical Pharmacology, Faculty of Medicine, Sivas Cumhuriyet University, Sivas, Turkey.ORCID http://orcid.org/0000-0003-2056-8683
İlkay KüçükgüzelDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Marmara University, P.O. Box: 34668, Istanbul, Turkey. ikucukguzel@marmara.edu.tr.ORCID http://orcid.org/0000-0002-7188-1859
Sivas Cumhuriyet Üniversitesi · TRMarmara University · TR

Funding

ECZ-046 ECZ-046SAĞ-C-DRP-111115-0502 SAĞ-C-DRP-111115-0502
6 · The paper itself

Abstract

4-Thiazolidinones and phenylaminopyrimidines are known as anticancer agents. Imatinib is the pioneer phenylaminopyrimidine derivative kinase inhibitor, which is used for the treatment of chronic myeloid leukemia. With a hybrid approach, a novel series of 5-benzylidene-2-arylimino-4-thiazolidinone derivatives containing phenylaminopyrimidine core were designed, synthesized, and tested for their anticancer activity on K562 (chronic myeloid leukemia), PC3 (prostat cancer), and SHSY-5Y (neuroblastoma) cells. Since superior anticancer activity was observed on K562 cells, further biological studies of selected compounds (8, 15, and 34) were performed on K562 cells. For the synthesis of designed compounds, thiourea compounds were converted to 2-imino-1,3-thiazolidin-4-ones with α-chloroacetic acid in the presence of sodium acetate. 5-Benzylidene-2-imino-1,3-thiazolidin-4-one derivatives were obtained by Knoevenagel condensation of 2-imino-1,3-thiazolidin-4-ones with related aldehydes. Compounds 8, 15, and 34 were evaluated for cell viability, apoptosis studies, cell cycle experiments, and DNA damage assays. IC

Indexed as

Antineoplastic AgentsProtein Kinase InhibitorsPyrimidinesThiazolidinesApoptosisCell CycleCell Line, TumorCell SurvivalDNA DamageDrug DesignHumansMolecular Docking SimulationProto-Oncogene Proteins c-abl4-thiazolidinoneAntineoplastic AgentsProtein Kinase InhibitorsProto-Oncogene Proteins c-ablPyrimidinesThiazolidines2-Arylimino-4-thiazolidinone derivativesAnticancer agentsApoptosisMolecular dockingPhenylaminopyrimidines

Identifiers

PMID32328961
OpenAlexW3018941124

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.