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Athamanta sicula L. Root extract: in vitro and in silico evaluation of anti-diabetic and anti-Alzheimer’s activities of apiol and myristicin

  • Khaled Aggoun
  • , Şevki Adem
  • , Zeyad Adil Hameed
  • , Federica POLLASTRO
  • , Brahim Harkati
  • , Hocine Laouer
  • , Stefano Salamone

Research output: Contribution to journalArticlepeer-review

Abstract

This study is the first to analyse the methanolic root extract of Athamanta sicula L., an endemic Mediterranean plant, leading to the isolation of two phenylpropanoids: apiol and myristicin. The extract and isolated compounds were evaluated for their inhibitory potential against α-amylase, α-glucosidase, acetylcholinesterase (AChE), and butyrylcholinesterase (BChE) using in vitro assays, molecular docking, and ADME predictions. The crude extract demonstrated superior inhibition of α-amylase and α-glucosidase compared to acarbose. Among the isolated compounds, apiol showed more activity than myristicin, particularly against α-glucosidase. Both compounds inhibited BChE, with apiol (IC50 = 330.07 µM; MolDock score = −89.89) outperforming myristicin (IC50 = 385.08 µM; MolDock score = −87.86). Favourable ADME properties, including high gastrointestinal absorption and blood-brain barrier penetration, were also predicted. These findings suggest that apiol and myristicin are key contributors to the plant’s bioactivity, making them promising multi-target lead compounds for developing new treatments for diabetes and Alzheimer’s disease.
Original languageEnglish
Pages (from-to)1-7
Number of pages7
JournalNatural Product Research
DOIs
Publication statusPublished - 2026

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • ADME
  • Alzheimer
  • Athamanta sicula
  • apiol
  • diabetes
  • molecular docking
  • myristicin

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