Synergistic action of phytoconstituents drives the anthelmintic potential of Croton penduliflorus stem bark extracts
The growing resistance to anthelmintic drugs highlights the urgent need for new, plant-derived therapeutics. This study investigates the synergistic anthelmintic activity of Croton penduliflorus stem bark extracts. Soxhlet extraction yielded 3.06% from the stem bark, with phytochemical screening revealing sterols as dominant constituents. The stem bark extract showed strong activity against Eudrilus eugeniae, causing paralysis and death within 8 ± 0.6 and 15 ± 0.5 min respectively at 100 mg/mL, with the ethyl acetate fraction being the most potent. GC–MS profiling identified key bioactive phytoconstituents including hexadecanamide, oleamide, and 1-heptacosanol—compounds known to disrupt membrane integrity, induce oxidative stress, and interfere with neuromuscular function. Molecular docking showed moderate binding affinity to β-tubulin, while molecular dynamics simulations revealed short-lived protein-ligand interactions, suggesting a non-exclusive tubulin targeting mechanism. The rapid anthelmintic response, combined with effects among fatty acid amides, sterols, and phenolics, suggests a multifactorial mode of action. These results support the traditional use of C. penduliflorus and underscore its stem bark as a promising source of synergistically acting lead compounds for novel anthelmintic drug development.
Authors
- Michael Konney Laryea (ORCID: https://orcid.org/0000-0002-9321-8898)
- Jehoshaphat Oppong Mensah (ORCID: https://orcid.org/0000-0003-4676-9299)
- Kwadwo Owusu (ORCID: https://orcid.org/0000-0003-1322-0566)
- Lawrence Sheringham Borquaye
- Selina Achiaa Owusu (ORCID: https://orcid.org/0000-0003-1888-4193)
Institutions
- Kwame Nkrumah University of Science and Technology (GH)
Publication Details
- Journal
- Discover Chemistry.
- Published
- 2025-08-26
- DOI
- https://doi.org/10.1007/s44371-025-00265-1
- Primary Topic
- Insect Pest Control Strategies
- Type
- article
- Field-Weighted Citation Impact
- 0.00