Evidence map›Paper›PMID 38271403›Full record

ArticlePloS one2024

Thymoquinone-protoflavone hybrid molecules as potential antitumor agents.

Sara H H Ahmed, Bizhar A Tayeb, Tímea Gonda, Gábor Girst, Kornél Szőri, Róbert Berkecz, István Zupkó, Renáta Minorics, Attila Hunyadi

Abstract read
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Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

9 authors.

Sara H H AhmedInstitute of Pharmacognosy, University of Szeged, Szeged, Hungary.
Bizhar A TayebInstitute of Pharmacodynamics and Biopharmacy, University of Szeged, Szeged, Hungary.ORCID 0000-0001-5197-564X
Tímea GondaInstitute of Pharmacognosy, University of Szeged, Szeged, Hungary.
Gábor GirstInstitute of Pharmacognosy, University of Szeged, Szeged, Hungary.
Kornél SzőriInstitute of Pharmacognosy, University of Szeged, Szeged, Hungary.
Róbert BerkeczInstitute of Pharmaceutical Analysis, University of Szeged, Szeged, Hungary.
István ZupkóInstitute of Pharmacodynamics and Biopharmacy, University of Szeged, Szeged, Hungary.
Renáta MinoricsInstitute of Pharmacodynamics and Biopharmacy, University of Szeged, Szeged, Hungary.
Attila HunyadiInstitute of Pharmacognosy, University of Szeged, Szeged, Hungary.ORCID 0000-0003-0074-3472

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe herein the synthesis of eight new ester-coupled hybrid compounds from thymoquinone and protoflavone building blocks, and their bioactivity testing against multiple cancer cell lines. Among the hybrids, compound 14 showed promising activities in all cell lines studied. The highest activities were recorded against breast cancer cell lines with higher selectivity to MDA-MB-231 as compared to MCF-7. Even though the hybrids were found to be completely hydrolysed in 24 h under cell culture conditions, compound 14 demonstrated a ca. three times stronger activity against U-87 glioblastoma cells than a 1:1 mixture of its fragments. Further, compound 14 showed good tumour selectivity: it acted 4.4-times stronger on U-87 cells than on MRC-5 fibroblasts. This selectivity was much lower, only ca. 1.3-times, when the cells were co-treated with a 1:1 mixture of its non-coupled fragments. Protoflavone-thymoquinone hybrids may therefore serve as potential new antitumor leads particularly against glioblastoma.

Indexed as

Antineoplastic AgentsGlioblastomaBenzoquinonesCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorHumansMolecular StructureStructure-Activity RelationshipAntineoplastic AgentsBenzoquinonesthymoquinone

Identifiers

PMID38271403
PMCPMC10810434

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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.