ArticleViewAbstractPharmacognosy Journal,2025,17,1,99-106.DOI:10.5530/pj.2025.17.14Published:January 2025Type:Research ArticleIn Vitro Antibacterial Activity, In-Silico Molecular Docking and Pharmacokinetic Profile of a Phytosterol Isolated from The Leaves of Carissa BispinosaWanda Shekwa, Mashilo Mash Matotoka, Tsolanku Sydney Maliehe, and Peter Masoko Wanda Shekwa, Mashilo Mash Matotoka, Tsolanku Sydney Maliehe, Peter Masoko* Department of Biochemistry, microbiology and Biotechnology, University of Limpopo, Private bag X1106, Sovenga 0727, SOUTH AFRICA. Abstract:Carissa bispinosa (L.) Desf. Ex-Brenan is a medicinal plant widely used in South Africa. The study reports on the isolation of a phytosterol from C. bispinosa along with molecular docking and pharmacokinetic studies. The phytochemicals were extracted with hexane, dichloromethane, acetone and methanol. The compound was isolated following a bioactivity-guided isolation protocol using column-chromatography and thin-layer chromatography. Nuclear magnetic resonance (NMR) was used for compound characterisation. The antimicrobial activity was assessed using bioautography and micro-broth dilution assays. AutoDock vina, SwissADME and ADMET lab were used for molecular docking, pharmacokinetic and toxicological properties, respectively. Drug-likeness was evaluated based on Lipinski's rule of five (Ro5). The isolated compound was identified as β-sitosterol. It had an anti-S. aureus activity of (0.31 mg/mL). It revealed binding scores of -7.2 and -6.4 kcal/mol against penicillin-binding protein and DNA gyrase, respectively. It violated one of Ro5 (MLOGP > 4.15). It has no inhibitory effects against isoforms of cytochrome P450. Moreover, it demonstrated no adverse effect on skin, non-carcinogenic and non-hepatotoxic effects. Based on the results, β-sitosterol can be considered as potential anti-S. aureus drug. Further studies may focus on ascertaining the mechanism of action in-vitro and investigating the synergistic effects of the compound with conventional drugs. Keywords:Antimicrobial, Carissa bispinosa, Molecular docking, PharmacokineticsView:PDF (534.66 KB) PDF Images 3D (left) and 2D (right) showing the interactions of β-sitosterol and with (A) penicillin-binding protein, (B) DNA gyrase and gentamicin against (C) Penicillin binding protein and (D) DNA gyrase. ‹ Comprehensive Antioxidant Evaluation of Tiliacora triandra Extracts: Assays of Leaf, Stem, and Root up Health Action Process Approach in Non-Communicable Diseases: A Systematic Review ›