Fomene Tsapy Raphaelle1,
Ache Roland Ndifor2,3 ,
Ngnintedo Dominique1,
Ambassa Pantaléon1,
Céline Henoumont4,
Njinga Ngaitad Stanislaus5,
Sophie Laurent4,6,
Fotso Wabo Ghislain1,
Ngameni Bathelemy7,
Bonaventure Tchaleu Ngadjui1,8
For correspondence:- Ache Ndifor Email: rolyndifor@gmail.com Tel:+237-676 444 329
Received: 15 February 2025 Accepted: 20 May 2025 Published: 31 May 2025
Citation: Raphaelle FT, Ndifor AR, Dominique N, Pantaléon A, Henoumont C, Stanislaus NN, et al. Isolation and evaluation of the antibacterial constituents of Synsepalum brevipes. Trop J Pharm Res 2025; 24(5):711-717 doi: https://dx.doi.org/10.4314/tjpr.v24i5.9
© 2025 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Purpose: To isolate and evaluate the antibacterial constituents of Synsepalum brevipes. Methods: The compounds were isolated using varying chromatographic separation methods. The structures were established using 1D and 2D nuclear magnetic resonance (NMR) spectroscopic methods, mass spectroscopy (MS), and by comparison with existing data. Extracts, fractions, and selected compounds were assessed against six bacterial strains using the broth microdilution method. Results: Chemical constituents isolated were identified as taraxeryl acetate, taraxerol, ursolic acid, oleanolic acid, betulinic acid, lupeol, herannone, spinasterol, spinasterol-3-O-β-D-glucopyranoside, eicosanoic acid, asperphernamate, hyperoside, spinasterone, arganin C, and butyroside B. The crude extracts and fractions were inactive against all the bacterial strains. The three compounds, which include oleanolic acid, ursolic acid, and hyperoside, exhibited moderate inhibitory activity with minimum inhibitory concentration (MIC) ranging from 12.5 to 50 μg/mL against the tested bacteria. Oleanolic acid revealed moderate bactericidal effects on Escherichia coli, and methicillin-resistant Staphylococcus (minimum bactericidal concentration (MBC) = 100 μg/mL, while ursolic acid showed moderate bactericidal effects on methicillin-resistant Staphylococcus aureus (MBC = 50 μg/mL). Conclusion: These results show that two triterpenoids and one phenolic exhibit moderate antibacterial effects against Escherichia coli, methicillin-resistant Staphylococcus, and Staphylococcus aureus
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