Evidence map›Paper›PMID 42021532›Full record

ArticleJournal of biochemical and molecular toxicology2026

Synthesis, Characterization, and Cytotoxic Activity Properties of Some Novel Purine Derivatives.

Nurdan Akdoğan, Ayşenur Işgüzar, Senem Akkoc, Muhammed Tilahun Muhammed, Sadeq K Alhag, Laila A Al-Shuraym, Ali Dişli

Abstract read
In one paragraph

Article in Journal of biochemical and molecular toxicology, 2026. 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

7 authors.

Nurdan AkdoğanDepartment of Chemistry, Institute of Science, Gazi University, Ankara, Türkiye.ORCID https://orcid.org/0000-0002-5361-7616
Ayşenur IşgüzarDepartment of Chemistry, Institute of Science, Gazi University, Ankara, Türkiye.ORCID https://orcid.org/0009-0006-9642-778X
Senem AkkocDepartment of Basic Pharmaceutical Sciences, Faculty of Pharmacy, Suleyman Demirel University, Isparta, Türkiye.ORCID https://orcid.org/0000-0002-1260-9425
Muhammed Tilahun MuhammedDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Suleyman Demirel University, Isparta, Türkiye.ORCID https://orcid.org/0000-0003-0050-5271
Sadeq K AlhagHealth Specialties, Basic Sciences and Applications Unit, Applied College, King Khalid University, Mohayil Asir, Saudi Arabia.ORCID https://orcid.org/0000-0001-6695-6492
Laila A Al-ShuraymBiology Department, Faculty of Science, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.ORCID https://orcid.org/0000-0002-1378-9579
Ali DişliDepartment of Chemistry, Faculty of Science, Gazi University, Ankara, Türkiye.ORCID https://orcid.org/0000-0002-5409-8838

Funding

Deanship of Scientific Research at King Khalid University for the funding support through the Large Research Groups Program R.G.P.2/7/47Princess Nourah bint Abdulrahman University for supporting this study via the Researchers Supporting Project PNURSP2026R365Suleyman Demirel University Research Fund TSG-2024-9516Türkiye Bilimsel ve Teknolojik Arastirma KurumuTÜrkiye Bilimsel ve Teknolojik AraŞtırma Kurumu
6 · The paper itself

Abstract

This study reports the synthesis of nine new compounds with purine scaffolds. It thoroughly analyzes them using a variety of spectroscopic methods, including high-resolution mass spectrometry (HR-MS), proton nuclear magnetic resonance (¹H NMR), attached proton test nuclear magnetic resonance (¹³C APT NMR), and fourier-transform infrared spectroscopy (FT-IR). The in vitro cytotoxic potential of these compounds was examined using two cancer cell lines: MDA-MB-231, a model of triple-negative breast cancer, and HepG2, a model of liver carcinoma. Furthermore, compounds were tested in a normal mouse fibroblast cell line (L929). Biological screening revealed that two of the synthesized molecules, ethyl 2-(2-(2-(9H-purin-6-yl)hydrazineylidene)-3-(4-methylphenyl)-4-oxothiazolidin-5-ylidene)acetate (4b) and ethyl 2-(2-(2-(9H-purin-6-yl)hydrazineylidene)-3-(4-nitrophenyl)-4-oxothiazolidin-5-ylidene)acetate (4c) exerted cytotoxic effects with IC

Indexed as

Antineoplastic AgentsPurinesAnimalsHep G2 CellsHumansMDA-MB-231 CellsMiceMolecular Docking SimulationAntineoplastic AgentsPurinescytotoxic activitydockingMD simulationPIpurine

Identifiers

PMID42021532
PMCPMC13103636

What OpenQuestion holds

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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.