Related Experiment Video
Updated: Feb 4, 2026

The Identification of Sea Lamprey Pheromones Using Bioassay-Guided Fractionation
Published on: July 17, 2018
Bioassay-guided fractionation and identification of wound healing active compounds from Khaya senegalensis leaves
Akrimi Najihah Mohd Khamil1,2, Norizamimie Nordin1, Mohamad Afiq Aizuddin Rosdi3
1Malaysian Institute of Pharmaceuticals and Nutraceuticals, National Institutes of Biotechnology Malaysia, Gelugor, Penang, Malaysia.
Abstract:
This study investigated the wound healing potential of Khaya senegalensis leaves through a comprehensive approach, including phytochemical, antioxidant, cytotoxicity, migration, and molecular docking analyses. Bioassay-guided isolation identified β-sitosterol and stigmasterol, with structures confirmed by NMR and FTIR analyses. Phytochemical screening revealed the presence of flavonoids, saponins, triterpenoids, tannins, and steroids, with solvent polarity significantly influencing composition. The ethyl acetate extract exhibited the strongest DPPH radical scavenging (IC₅₀ = 5.6 mg/mL). The methanol extract had the highest total phenolic content (198.8 mg GAE/g) while the ethyl acetate had the highest flavonoid content (1,228.1 mg QE/g). MTT assays confirmed the cytocompatibility of all extracts, fractions, and isolated compounds in HaCaT and HDF cells (>50% viability at ≤100 µg/mL). Scratch assays demonstrated significant, concentration-dependent wound closure, with optimal effects at 12.5 μg/mL. The most active fraction (1.2H) and subfractions (1.2.1H, 1.2.3H), as well as the isolated compounds, achieved complete wound closure in HDF cells within 24 hours. Molecular docking revealed strong binding of β-sitosterol and stigmasterol with TNF-α and GSK-3β, supporting their role in modulating inflammatory and proliferative pathways. These findings highlight Khaya senegalensis as a promising candidate for promoting wound repair, exerting antioxidant, cytocompatible, and pro-migratory effects.
Related Concept Videos
Leaving Groups
In general, in a nucleophilic substitution reaction, a nucleophile displaces a functional group, called the leaving group, from the substrate to give a substituted product. A leaving group departs the substrate molecule through heterolytic cleavage, taking the pair of electrons with it to become a relatively stable weak base in the form of an anion or a neutral molecule.
In a...
Molecules and Compounds
Organic Compounds
Elements and Compounds
Elements
Elements are classified as atomic or molecular based on the nature of their basic units. They are unique forms of matter with specific chemical and physical properties that cannot break down into smaller substances by ordinary chemical reactions. There...
Effect of Hepatic Disease on Pharmacokinetics: Active Drug, Metabolite and Fraction of Metabolized Drug
Solubility of Ionic Compounds

