Evidence map›Paper›PMID 38643226›Full record

ArticleScientific reports2024

Synthesis, biofilm formation inhibitory, and inflammation inhibitory activities of new coumarin derivatives.

Ghada E Ahmed, Zeinab A Elshahid, Eslam Reda El-Sawy, Mohamed S Abdel-Aziz, Anhar Abdel-Aziem

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

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  9. Discovery ofFrontiers in chemistry · 2025
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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 3 institutions in 1 country.

Ghada E AhmedHigh Canal Institute of Engineering & Technology, Suez, Egypt.
Zeinab A ElshahidChemistry of Natural and Microbial Products Department, Pharmaceutical and Drug Industries Research Institute, National Research Centre, Giza, Egypt.
Eslam Reda El-SawyChemistry of Natural Compounds Department, National Research Centre, Dokki, Giza, 12622, Egypt.
Mohamed S Abdel-AzizMicrobial Chemistry Department, Genetic Engineering and Biotechnology Institute, National Research Centre, Dokki, Giza, 12622, Egypt.
Anhar Abdel-AziemChemistry Department, Faculty of Science (Girl's Branch), Al-Azhar University, Cairo, 11754, Egypt. anhar@azhar.edu.eg.
National Research Centre · EGAl-Azhar University · EGSuez University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coumarins are heterocycles of great interest in the development of valuable active structures in chemistry and biological domains. The ability of coumarins to inhibit biofilm formation of Gram positive bacterium (Staphylococcus aureus), Gram negative bacterium (Escherichia coli) as well as the methicillin-resistant S. aureus (MRSA) has been previously described. In the present work, new hybrid coumarin-heterocycles have been synthesized via the reaction of coumarin-6-sulfonyl chloride and 6-aminocoumarin with different small heterocycle moieties. The biological efficacy of the new compounds was evaluated towards their ability to inhibit biofilm formation and their anti-inflammatory properties. The antimicrobial activities of the newly synthesized compounds were tested against Gram positive bacterium (S. aureus ATCC 6538), Gram negative bacterium (E. coli ATCC 25922), yeast (Candida albicans ATCC 10231) and the fungus (Aspergillus niger NRRL-A326). Compounds 4d, 4e, 4f, 6a and 9 showed significant MIC and MBC values against S. aureus, E. coli, C. albicans, and methicillin-resistant S. aureus (MRSA) with especial incidence on compound 9 which surpasses all the other compounds giving MIC and MBC values of (4.88 and 9.76 µg/mL for S. aureus), (78.13 and 312.5 µg/mL for E. coli), (9.77 and 78.13 µg/mL for C. albicans), and (39.06 and 76.7 µg/mL for MRSA), respectively. With reference to the antibiofilm activity, compound 9 exhibited potent antibiofilm activity with IC

Indexed as

Anti-Bacterial AgentsMethicillin-Resistant Staphylococcus aureusAnti-Inflammatory AgentsBiofilmsCoumarinsEscherichia coliGram-Negative BacteriaGram-Positive BacteriaHumansInflammationMicrobial Sensitivity TestsStaphylococcus aureusAnti-Bacterial AgentsAnti-Inflammatory AgentsCoumarins6-aminocoumarinAnti-inflammatoryAntimicrobialBiofilmCoumarin-6-sulfonyl chlorideHeterocycles

Identifiers

PMID38643226
PMCPMC11032357
OpenAlexW4394987954

What OpenQuestion holds

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LicenceCC BY
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.