Sylvestre Tsila Saidou

Mr. Sylvestre Tsila Saidou


Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 July 2025 in Molecules
Verified
Journal Article
Open access
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SSSylvestre Tsila Saidou
Sylvestre Tsila Saidou
MKMc Jesus Kinyok
Mc Jesus Kinyok
JTJoseph Eric Mbasso Tameko
Joseph Eric Mbasso Tameko
Bel Youssouf G. MountessouBel Youssouf G. Mountessou
Bel Youssouf G. Mountessou
KDKevine Johanne Jumeta Dongmo
Kevine Johanne Jumeta Dongmo
BNBruno Lenta Ndjakou
Bruno Lenta Ndjakou
Malaria continues to pose a significant global health burden, driving the search for novel antimalarial agents to address emerging drug resistance. This study evaluated the antiplasmodial potential of Ziziphus mauritiana Lam. (Rhamnaceae) roots through an integrated phytochemical and pharmacological approach. The ethanol extract, along with its derived fractions, demonstrated potent in vitro activity against the chloroquine-sensitive Plasmodium falciparum strain 3D7 (Pf3D7), with the ethyl acetate-soluble (IC50 = 11.35 µg/mL) and alkaloid-rich (IC50 = 4.75 µg/mL) fractions showing particularly strong inhibition. UHPLC-DAD-ESI-QTOF-MS/MS-based molecular networking enabled the identification of thirty-two secondary metabolites (1–32), comprising twenty-five cyclopeptide alkaloids (CPAs), five of which had not yet been described (11, 20, 22, 23, 25), and seven known triterpenoids. Bioactivity-guided isolation yielded thirteen purified compounds (5, 6, 14, 26–30, 32–36), with betulinic acid (30; IC50 = 19.0 µM) and zizyberenalic acid (32; IC50 = 20.45 µM) exhibiting the most potent antiplasmodial effects. Computational ADMET analysis identified mauritine F (4), hemisine A (10), and nummularine R (21) as particularly promising lead compounds, demonstrating favourable pharmacokinetic properties, low toxicity profiles, and predicted activity against both family A G protein-coupled receptors and evolutionarily distinct Plasmodium protein kinases. Quantitative analysis revealed exceptionally high concentrations of key bioactive constituents, notably zizyberenalic acid (24.3 mg/g) in the root extracts. These findings provide robust scientific validation for the traditional use of Z. mauritiana in malaria treatment while identifying specific cyclopeptide alkaloids and triterpenoids as valuable scaffolds for antimalarial drug development. The study highlights the effectiveness of combining advanced metabolomics, bioassay-guided fractionation, and computational pharmacology in natural product-based drug discovery against resistant malaria strains.

18 July 2024 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
PFPatrick Kevin Moto Feune
Patrick Kevin Moto Feune
PKPaulin Teko Keumedjio
Paulin Teko Keumedjio
SBSara Nathalie Edjenguèlè Béboy
Sara Nathalie Edjenguèlè Béboy
YJYannick Sani Jignoua
Yannick Sani Jignoua
FMFabiola Jenny Massah
Fabiola Jenny Massah
PMPaul Fewou Moundipa
Paul Fewou Moundipa