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Exploring the impact of the innovative compound 3-(3-(4-hydroxy-2-oxo-2H-chromen-3-yl)-5-(pyridin-3-yl)-1H-pyrazol-1-yl) indolin-2-one on accelerating wound recovery
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  • Published: 21 February 2026

Exploring the impact of the innovative compound 3-(3-(4-hydroxy-2-oxo-2H-chromen-3-yl)-5-(pyridin-3-yl)-1H-pyrazol-1-yl) indolin-2-one on accelerating wound recovery

  • Ahmed Sabt1,
  • Heba Abdelmegeed1,
  • Abdel-Razik H. Abdel-Razik2,
  • Mohamed G. Thabit3,
  • Marwa Balaha4,5,
  • Moataz A. Shaldam4,5,
  • Ahmed M. Reda6,7,
  • Ahmed A. F. Soliman8,
  • Mohamed Abdelraof9,
  • Nehad A. Abdel Latif1,
  • Mai M. Elghonemy1,
  • Eman Y. Ahmed1,
  • Mohamed A. Abdelrahman6,10 &
  • …
  • Rasha Z. Batran1 

Scientific Reports , Article number:  (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biochemistry
  • Biotechnology
  • Chemistry
  • Drug discovery
  • Microbiology

Abstract

Wound healing represents a significant challenge within the field of medical science. Contemporary clinical practices increasingly favor the utilization of herbal compounds to facilitate the repair process. Among these compounds, coumarin-a phytochemical noted for its antibacterial and wound-healing properties-has garnered considerable attention. This study investigates the potential advantages of incorporating coumarin into wound dressings within an experimental model. Our synthesized target compound 3-(3-(4-hydroxy-2-oxo-2H-chromen-3-yl)-5-(pyridin-3-yl)-1H-pyrazol-1-yl) indolin-2-one (CPPI) demonstrated notable antimicrobial activity against the pathogenic Staphylococcus aureus MRSA, Bacillus cereus, and Pseudomonas aeruginosa. Moreover, both in vitro and in vivo experiments showed that CPPI significantly enhanced the migration of skin fibroblast cells and promoted the wound healing process. Furthermore, it facilitated complete re-epithelialization of the wounds. Histological analysis revealed the formation of well-structured granulation tissue and a reduction in indicators of wound infection, evidenced by a minimal presence of inflammatory cells in comparison to untreated wounds. Additionally, in silico molecular docking studies of CPPI indicated significant binding affinity within COX-2 active site along with a stable complex during molecular dynamics simulations. Collectively, the findings of this study suggest that CPPI can provide a protective effect against infections in cutaneous wounds, attributable to its antimicrobial properties.

Data availability

All data generated or analyzed during this study are included in this published article and its supplementary information files.

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Funding

Open access funding provided by The Science, Technology & Innovation Funding Authority (STDF) in cooperation with The Egyptian Knowledge Bank (EKB). This research did not receive funding.

Author information

Authors and Affiliations

  1. Chemistry of Natural Compounds Department, Pharmaceutical and Drug Industries Research Institute, National Research Centre, Dokki, Cairo, 12622, Egypt

    Ahmed Sabt, Heba Abdelmegeed, Nehad A. Abdel Latif, Mai M. Elghonemy, Eman Y. Ahmed & Rasha Z. Batran

  2. Department of Histology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef, 62511, Egypt

    Abdel-Razik H. Abdel-Razik

  3. Department of Pharmaceutical Chemistry, Pharos University in Alexandria, Canal El Mahmoudia street, Beside Green Plaza complex, 21648, Alexandria, Egypt

    Mohamed G. Thabit

  4. Department of Pharmacy, “G. d’Annunzio” University of Chieti-Pescara, 66100, Chieti, Italy

    Marwa Balaha & Moataz A. Shaldam

  5. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh, 33516, Egypt

    Marwa Balaha & Moataz A. Shaldam

  6. College of Pharmacy, University of Kut, Wasit, 52001, Iraq

    Ahmed M. Reda & Mohamed A. Abdelrahman

  7. Department of Biochemistry, Faculty of Pharmacy, Egyptian Russian University, Badr City, Cairo, 11829, Egypt

    Ahmed M. Reda

  8. Pharmacognosy Department, Pharmaceutical and Drug Industries Research Institute, National Research Center, Dokki, Egypt

    Ahmed A. F. Soliman

  9. Microbial Chemistry Department, Biotechnology Research Institute, National Research Centre, 33 El Bohouth St, P.O.12622, Giza, Egypt

    Mohamed Abdelraof

  10. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Egyptian Russian University, Badr City, Cairo, 11829, Egypt

    Mohamed A. Abdelrahman

Authors
  1. Ahmed Sabt
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  2. Heba Abdelmegeed
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  3. Abdel-Razik H. Abdel-Razik
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  5. Marwa Balaha
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  6. Moataz A. Shaldam
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  8. Ahmed A. F. Soliman
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  9. Mohamed Abdelraof
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  10. Nehad A. Abdel Latif
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  11. Mai M. Elghonemy
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  14. Rasha Z. Batran
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Contributions

A.S., E.Y.A and R.Z.B contributed to conceptualization and design of the research work. A.S., E.Y.A, M.M.E and R.Z.B participated in the synthesis and purification of the compounds, and analysis of spectra data. H.A., A.H. A., A.A.F.S. and M.A. performed the biological tests. M.B. and M.A.S conducted molecular docking and dynamic simulations studies. M.G.T., A.M.R. and M.A.A. contributed to visualization. N.A.L. and R.Z.B contributed to supervision, A.S., H.A., A.H.A., M.B., M.A.S., A.A.F.S., M.A., E.Y.A. participated in writing and editing the original manuscript draft. All authors reviewed the manuscript.

Corresponding authors

Correspondence to Eman Y. Ahmed or Rasha Z. Batran.

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Competing interests

The authors declare no competing interests.

Ethical approval

This study was conducted according to the appropriate ethical standards as required by guidance from the Research Ethics Committee, Faculty of Pharmacy, Egyptian Russian University, Egypt, Ethical Approval No. ERUFP-PC-24005.

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Sabt, A., Abdelmegeed, H., Abdel-Razik, AR.H. et al. Exploring the impact of the innovative compound 3-(3-(4-hydroxy-2-oxo-2H-chromen-3-yl)-5-(pyridin-3-yl)-1H-pyrazol-1-yl) indolin-2-one on accelerating wound recovery. Sci Rep (2026). https://doi.org/10.1038/s41598-026-37714-5

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  • Received: 24 September 2025

  • Accepted: 23 January 2026

  • Published: 21 February 2026

  • DOI: https://doi.org/10.1038/s41598-026-37714-5

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Keywords

  • Coumarin
  • Heterocyclic
  • Antibacterial
  • Wound healing
  • In vivo study
  • Molecular modeling
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