Evidence map›Paper›PMID 39839233›Full record

ArticleRSC advances2025

Microwave-assisted synthesis and

Ashraf A Aly, Hisham A Abd El-Naby, Essam Kh Ahmed, Sageda A Gedamy, Kari Rissanen, Martin Nieger, Alan B Brown, Michael G Shehat, Marwa M Shaaban, Amal Atta

Abstract read
In one paragraph

Article in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

10 authors.

Ashraf A AlyChemistry Department, Faculty of Science, Minia University 61519 El-Minia Egypt ashrafaly63@yahoo.com ashraf.shehata@mu.edu.eg hisham_minia@mu.edu.eg essam.mohd@mu.edu.eg sagedaali332@yahoo.com.ORCID https://orcid.org/0000-0002-0314-3408
Hisham A Abd El-NabyChemistry Department, Faculty of Science, Minia University 61519 El-Minia Egypt ashrafaly63@yahoo.com ashraf.shehata@mu.edu.eg hisham_minia@mu.edu.eg essam.mohd@mu.edu.eg sagedaali332@yahoo.com.
Essam Kh AhmedChemistry Department, Faculty of Science, Minia University 61519 El-Minia Egypt ashrafaly63@yahoo.com ashraf.shehata@mu.edu.eg hisham_minia@mu.edu.eg essam.mohd@mu.edu.eg sagedaali332@yahoo.com.
Sageda A GedamyChemistry Department, Faculty of Science, Minia University 61519 El-Minia Egypt ashrafaly63@yahoo.com ashraf.shehata@mu.edu.eg hisham_minia@mu.edu.eg essam.mohd@mu.edu.eg sagedaali332@yahoo.com.
Kari RissanenDepartment of Chemistry, University of Jyväskylä P. O. Box 35 FIN-40014 Jyväskylä Finland kari.t.rissanen@jyu.fi.ORCID https://orcid.org/0000-0002-7282-8419
Martin NiegerDepartment of Chemistry, University of Helsinki P. O. Box 55, A. I. Virtasen aukio I 00014 Helsinki Finland martin.nieger@helsinki.fi.
Alan B BrownDepartment of Chemistry and Chemical Engineering, Florida Institute of Technology Melbourne FL 32901 USA abrown@fit.edu.
Michael G ShehatDepartment of Microbiology, Faculty of Pharmacy, Alexandria University Alexandria 21521 Egypt michael.shehat@alexu.edu.eg.
Marwa M ShaabanDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Alexandria University Alexandria 21521 Egypt maraw.mamdouh@alexu.edu.eg amal.atta@alexu.edu.eg missalex_pharma@yahoo.com.
Amal AttaDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Alexandria University Alexandria 21521 Egypt maraw.mamdouh@alexu.edu.eg amal.atta@alexu.edu.eg missalex_pharma@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A microwave-assisted method was utilized to synthesize novel pyranoquinolone derivatives as dual acting topoisomerase II/DNA gyrase inhibitors with apoptosis induction ability for halting lung cancer and staphylococcal infection. Herein, the designed rationale was directed toward mimicking the structural features of both topoisomerase II and DNA gyrase inhibitors as well as endowing them with apoptosis induction potential. The absolute configuration of the series was assigned using X-ray diffraction analysis. Cytotoxic activity against NSCLC A549 cells showed that ethyl 2-amino-9-bromo-4-(furan-2-yl)-5-oxo-5,6-dihydro-4

Identifiers

PMID39839233
PMCPMC11749604

What OpenQuestion holds

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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.