Antibacterial and DPPH Radical Inhibitory Activities and Molecular Simulation of Compounds Isolated from the Leaves of .

is one of the medicinal plants traditionally used in Ethiopia to treat various ailments, including wounds, snake bites, tuberculosis, and cancer. However, there is a lack of comprehensive investigation regarding the biological activities of the phytoconstituents extracted from its leaves. This study aims to isolate compounds and evaluate their antibacterial properties and DPPH radical scavenging activities, complemented by molecular modeling. Thirteen compounds were identified using GC-MS from combined fractions 4-17. Ursolic acid (), 5-hydroxy-4-methyl-5,6-dihydro-(2)-pyran-2-one (), hyperoside (), and 4--β-d-glucopyranosylcaffeic acid () were purified using chromatographic techniques and characterized using 1D and 2D NMR spectral data and a thorough comparison with literature data. At 5 mg/mL, the inhibition zones (IZs) of isolated compounds ranged from 9.00 to 12.67 mm against all of the evaluated bacteria. Among all isolated compounds, compound exhibited more inhibition against with an inhibition zone of 12.67 mm, and compound also exhibited potent inhibition activity against with an inhibition zone of 11.00 mm. and were better inhibited using compound with IZs of 12.30 and 11.70 mm, respectively. The antibacterial activity of compound against and was validated using molecular docking studies against the target enzymes DNA gyrase B (-8.4 kcal/mol) and quinolone signal A (-9.3 kcal/mol), respectively. At 62.5 μg/mL, the highest (89.2%) and the lowest (50.5%) DPPH radicals were scavenged by compounds and , respectively. Compounds , , and obey Lipinski's rule of five, and none of the isolated compounds were predicted to be fatal if swallowed. These findings reinforce the traditional use of the plant as a remedy for various bacterial diseases. However, further studies are essential to assess the biological and toxicological properties of the isolated compounds.