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Synthesis and biological evaluation of 6-hydroxychromone based thiosemicarbazones as potential antidiabetic and antioxidant agents
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  • Published: 22 February 2026

Synthesis and biological evaluation of 6-hydroxychromone based thiosemicarbazones as potential antidiabetic and antioxidant agents

  • Wajeeha Zareen1,
  • Nadeem Ahmed1,2,
  • Farhan Siddique3,
  • Parham Taslimi4,
  • Muhammad Ali Khan1,
  • Talha Islam5,
  • Mostafa A. Ismail6,
  • Mariya al-Rashida5,
  • Magdi E. A. Zaki7,
  • Sobhi M. Gomha8,
  • Rima D. Alharthy9 &
  • …
  • Zahid Shafiq1 

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
  • Chemical biology
  • Chemistry
  • Computational biology and bioinformatics
  • Drug discovery

Abstract

A new series of 6-hydroxychromone-based thiosemicarbazones 4(a-p) was synthesized and assessed for their antidiabetic (α-Glucosidase and α-Amylase inhibition) as well as antioxidant (2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2´-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS)) activities. Among the synthesized compounds, compound 4k (IC50 = 1.18 ± 0.19 µg/mL) emerged as the promising α-Glucosidase inhibitor, significantly outperforming the reference drug Acarbose (IC50 = 7.33 ± 0.13 µg/mL). For α-Amylase inhibition, compound 4 g (IC50 = 13.61 ± 2.04 µg/mL) demonstrated excellent activity, compared to Acarbose (IC50 = 43.15 ± 5.22 µg/mL). In antioxidant assays, compound 4o (IC50 = 15.30 ± 1.70 µg/mL) exhibited the strongest DPPH radical scavenging effect, and compound 4 g (IC50 = 6.06 ± 0.15 µg/mL) showed the highest ABTS scavenging activity, surpassing the standard antioxidant Trolox (IC50 = 30.20 ± 5.14 & 18.19 ± 2.47 µg/mL, respectively). Remarkably, these derivatives showed greater efficacy compared to standard inhibitors, underscoring their promise as novel candidates for antidiabetic and antioxidant drug development. Molecular docking analysis demonstrated strong binding and critical interactions within the enzyme active sites. MD simulations confirmed the stability of 4k-α-Glucosidase and 4 g-α-Amylase, with RMSD values below 3.6 Å, low RMSF (< 2.8 Å) at the binding site, and sustained key interactions with Phe 158 and Tyr 151, respectively. The network pharmacology further supported the findings of molecular docking and simulation analysis.

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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Acknowledgements

The authors express their appreciation to the Deanship of Scientific Research at King Khalid University, Saudi Arabia, for this work through Large Research Project under grant number RGP-2/691/46.

Funding

The authors express their appreciation to the Deanship of Scientific Research at King Khalid University, Saudi Arabia, for this work through Large Research Project under grant number RGP-2/691/46.

Author information

Authors and Affiliations

  1. Institute of Chemical Sciences, Bahauddin Zakariya University, 60800, Multan, Pakistan

    Wajeeha Zareen, Nadeem Ahmed, Muhammad Ali Khan & Zahid Shafiq

  2. College of Chemistry & Chemical Engineering, Central South University, Changsha, 410083, Hunan, China

    Nadeem Ahmed

  3. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Bahauddin Zakariya University, Multan, 60800, Pakistan

    Farhan Siddique

  4. Department of Biotechnology, Faculty of Science, Bartin University, 74110, Bartin, Turkey

    Parham Taslimi

  5. Department of Chemistry, Forman Christian College (A Chartered University), Ferozepur Road 54600, Lahore, Pakistan

    Talha Islam & Mariya al-Rashida

  6. Department of Chemistry, Faculty of Science, Research Center for Advanced Materials Science (RCAMS), King Khalid University, P.O. Box 960, Abha, 61421, Saudi Arabia

    Mostafa A. Ismail

  7. Department of Chemistry, Faculty of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh, 11623, Saudi Arabia

    Magdi E. A. Zaki

  8. Department of Chemistry, Faculty of Science, Islamic University of Madinah, Madinah, 42351, Saudi Arabia

    Sobhi M. Gomha

  9. Department of Chemistry, Rabigh Branch, Science & Arts College, King Abdulaziz University, Rabigh, 21911, Saudi Arabia

    Rima D. Alharthy

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  1. Wajeeha Zareen
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Contributions

Wajeeha Zareen, Farhan Siddique: Investigation, Formal analysis. Nadeem Ahmed : Writing – original draft, Validation. Mostafa A. Ismail, Rima D. Alharthy: Formal analysis, software, Funding acquisition. Parham Taslimi, Mariya al-Rashida, Talha Islam: Formal analysis, software, Data curation, Investigation. Supervision, Conceptualization. Magdi E. A. Zaki, Sobhi M. Gomha: Formal analysis, Data curation, Funding acquisition. Zahid Shafiq, Ali Muhamad Khan : Writing – original draft, Supervision, Conceptualization.

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Correspondence to Sobhi M. Gomha or Zahid Shafiq.

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Zareen, W., Ahmed, N., Siddique, F. et al. Synthesis and biological evaluation of 6-hydroxychromone based thiosemicarbazones as potential antidiabetic and antioxidant agents. Sci Rep (2026). https://doi.org/10.1038/s41598-026-40449-y

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  • Received: 05 November 2025

  • Accepted: 12 February 2026

  • Published: 22 February 2026

  • DOI: https://doi.org/10.1038/s41598-026-40449-y

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Keywords

  • 6-Hydroxychromone
  • Thiosemicarbazones
  • Antidiabetic
  • Antioxidant
  • Enzyme inhibition
  • Molecular docking
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