Evidence map›Paper›PMID 40610494›Full record

ArticleScientific reports2025

Synthesis, comprehensive in silico studies, and cytotoxicity evaluation of novel quinazolinone derivatives as potential anticancer agents.

David S A Haneen, Abdelaal A Abdalha, Musaab M Alkhatib, Mahmoud Kamal, Ahmed S A Youssef, Wael S I Abou-Elmagd, Sandy S Samir

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. New Quinazolin-4(3Molecules (Basel, Switzerland) · 2025
    Article
  6. 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

7 authors.

David S A HaneenChemistry Department, Faculty of Science, Ain Shams University, Abbassia, Cairo, 11566, Egypt. david.shoukry@sci.asu.edu.eg.ORCID http://orcid.org/0000-0002-8085-2910
Abdelaal A AbdalhaChemistry Department, Faculty of Science, Ain Shams University, Abbassia, Cairo, 11566, Egypt.ORCID http://orcid.org/0000-0002-2573-1681
Musaab M AlkhatibChemistry Department, Faculty of Science, Ain Shams University, Abbassia, Cairo, 11566, Egypt.ORCID http://orcid.org/0000-0002-1964-7432
Mahmoud KamalEntomology Department, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt.ORCID https://orcid.org/0000-0001-7447-0433
Ahmed S A YoussefChemistry Department, Faculty of Science, Ain Shams University, Abbassia, Cairo, 11566, Egypt.ORCID http://orcid.org/0000-0001-5912-4874
Wael S I Abou-ElmagdChemistry Department, Faculty of Science, Ain Shams University, Abbassia, Cairo, 11566, Egypt.ORCID http://orcid.org/0000-0002-8317-3972
Sandy S SamirChemistry Department, Faculty of Science, Ain Shams University, Abbassia, Cairo, 11566, Egypt.ORCID http://orcid.org/0000-0002-5637-8200

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quinazolinone derivatives exhibit significant synthetic and biological properties, making them valuable candidates for anticancer drug development. In this study, we synthesized novel quinazolinone derivatives via reactions of the previously unreported 4H-benzoxazin-4-one derivative (2) with various nitrogen nucleophiles, such as hydrazine hydrate and ammonium acetate, which yielded hydrazide and quinazolinone derivatives (3-6). Further modifications were achieved through reactions with carbon electrophiles and carbonyl compounds (e.g., phthalic anhydride, phenyl isothiocyanate, potassium cyanate, and pyrazole carbaldehyde), resulting in an expanded library of novel quinazolinone derivatives (7-15). The structures of all synthesized compounds were confirmed by spectroscopic and microanalytical techniques. In vitro cytotoxicity evaluations (mean IC

Indexed as

Antineoplastic AgentsQuinazolinonesCell Line, TumorDNA Topoisomerases, Type IIDrug Screening Assays, AntitumorErbB ReceptorsHumansMolecular Docking SimulationMolecular Dynamics SimulationProto-Oncogene Proteins c-metStructure-Activity RelationshipVascular Endothelial Growth Factor Receptor-2Antineoplastic AgentsDNA Topoisomerases, Type IIErbB ReceptorsProto-Oncogene Proteins c-metQuinazolinonesVascular Endothelial Growth Factor Receptor-2Anticancer agentsBenzoxazinoneComputational studiesCytotoxicityHydrazide derivativesMolecular dockingQuinazolinone

Identifiers

PMID40610494
PMCPMC12229541

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Registered trials

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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.