<i>In Vitro</i> Antibacterial and DPPH RadicalInhibitory Activities and <i>In Silico</i> Molecular Simulationof Compounds Isolated from the Leaves of Olinia rochetiana

Olinia rochetiana 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 <i>in vitro</i> antibacterial properties and DPPH radical scavenging activities, complemented by <i>in silico</i> molecular modeling. Thirteen compounds were identified using GC–MS from combined fractions 4–17. Ursolic acid (<b>14</b>), 5-hydroxy-4-methyl-5,6-dihydro-(2<i>H</i>)-pyran-2-one (<b>15</b>), hyperoside (<b>16</b>), and 4-<i>O</i>-β-d-glucopyranosylcaffeic acid (<b>17</b>) 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 <b>14</b> exhibited more inhibition against Streptococcus pyogenes with an inhibition zone of 12.67 mm, and compound <b>17</b> also exhibited potent inhibition activity against Staphylococcus aureus with an inhibition zone of 11.00 mm. Escherichia coli and Pseudomonas aeruginosa were better inhibited using compound <b>16</b> with IZs of 12.30 and 11.70 mm, respectively. The antibacterial activity of compound <b>16</b> against E. coli and P. aeruginosawas validated using <i>in silico</i> molecular docking studies against the target enzymes E. coli DNA gyrase B (−8.4 kcal/mol) and <i>Pseudomonas</i> 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 <b>16</b> and <b>14</b>, respectively. Compounds <b>14</b>, <b>15</b>, and <b>17</b> 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 <i>in vivo</i> studies are essential to assess the biological and toxicological properties of the isolated compounds.

Publication Details

Journal
Figshare
Published
2025-02-27
DOI
https://doi.org/10.1021/acsomega.4c10788.s001
Primary Topic
Natural product bioactivities and synthesis
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article
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article

In Vitro Antibacterial and DPPH RadicalInhibitory Activities and In Silico Molecular Simulationof Compounds Isolated from the Leaves of Olinia rochetiana

Figshare
Natural product bioactivities and synthesis
article

In Vitro Antibacterial and DPPH RadicalInhibitory Activities and In Silico Molecular Simulationof Compounds Isolated from the Leaves of Olinia rochetiana

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Abstract

Olinia rochetiana 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 <i>in vitro</i> antibacterial properties and DPPH radical scavenging activities, complemented by <i>in silico</i> molecular modeling. Thirteen compounds were identified using GC–MS from combined fractions 4–17. Ursolic acid (<b>14</b>), 5-hydroxy-4-methyl-5,6-dihydro-(2<i>H</i>)-pyran-2-one (<b>15</b>), hyperoside (<b>16</b>), and 4-<i>O</i>-β-d-glucopyranosylcaffeic acid (<b>17</b>) 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 <b>14</b> exhibited more inhibition against Streptococcus pyogenes with an inhibition zone of 12.67 mm, and compound <b>17</b> also exhibited potent inhibition activity against Staphylococcus aureus with an inhibition zone of 11.00 mm. Escherichia coli and Pseudomonas aeruginosa were better inhibited using compound <b>16</b> with IZs of 12.30 and 11.70 mm, respectively. The antibacterial activity of compound <b>16</b> against E. coli and P. aeruginosawas validated using <i>in silico</i> molecular docking studies against the target enzymes E. coli DNA gyrase B (−8.4 kcal/mol) and <i>Pseudomonas</i> 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 <b>16</b> and <b>14</b>, respectively. Compounds <b>14</b>, <b>15</b>, and <b>17</b> 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 <i>in vivo</i> studies are essential to assess the biological and toxicological properties of the isolated compounds.

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Natural product bioactivities and synthesis
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<i>In Vitro</i> Antibacterial and DPPH RadicalInhibitory Activities and <i>In Silico</i> Molecular Simulationof Compounds Isolated from the Leaves of Olinia rochetiana · Figshare (2025) | TGRS Research Map | TGRS