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Original Research Article | OPEN ACCESS

Isolation and evaluation of the antibacterial constituents of Synsepalum brevipes

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

1Department of Organic Chemistry, Faculty of Science, University of Yaoundé 1, Yaoundé, Cameroon; 2Higher Technical Teachers Training College, University of Bamenda, Cameroon; 3Department of Chemistry, Faculty of Science, University of Bamenda, Cameroon; 4General, Organic and Biomedical Chemistry, NMR and Molecular Imaging Laboratory, University of Mons, Place du Parc 20, 7000 Mons, Belgium; 5Department of Pharmaceutical and Medicinal Chemistry, University of Ilorin, Nigeria; 6Center for Microscopy and Molecular Imaging (CMMI), Rue Adrienne Bolland 8, 6041 Gosseilies, Belgium; 7Department of Pharmacognosy and Pharmaceutical Chemistry, Faculty of Medicine and Biomedical Sciences, University of Yaoundé, Cameroon; 8University Institute of Sciences, Technologies and Ethics Yaoundé, Cameroon.

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..

Abstract

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

Keywords: Synsepalum brevipes, Phytochemicals, Antibacterial activity, Sapotaceae

Impact Factor
Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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