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 language | English |
|---|---|
| Pages (from-to) | 1-7 |
| Number of pages | 7 |
| Journal | Natural Product Research |
| DOIs | |
| Publication status | Published - 2026 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- ADME
- Alzheimer
- Athamanta sicula
- apiol
- diabetes
- molecular docking
- myristicin
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