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Myxaoside A, a new triterpenoid saponin from Cordia myxa L. (Boraginaceae).
Bernard, Dabolé; Matthieu, Matcheme; Isaac Silvère, Gade; Djaouda, Moussa; Jean Noël, Nyemb; Diguir, Moïse; Clément, Saram; Emmanuel, Talla; Laurent, Sophie; Henoumont, Céline; Venditti, Alessandro; Alex De Theodore, Atchadé; Benoît, Loura.
Afiliação
  • Bernard D; Department of Chemistry, Faculty of science, University of Maroua, Maroua, Cameroon.
  • Matthieu M; Department of Refining and Petrochemistry, National Advanced School of Mines and Petroleum Industries, University of Maroua, Kaélé, Cameroon.
  • Isaac Silvère G; Department of Chemistry, Faculty of science, University of Maroua, Maroua, Cameroon.
  • Djaouda M; Department of Chemistry, Faculty of science, University of Maroua, Maroua, Cameroon.
  • Jean Noël N; Department of Life and Earth Sciences, Higher Teachers' Training College, University of Maroua, Maroua, Cameroun.
  • Diguir M; Department of Refining and Petrochemistry, National Advanced School of Mines and Petroleum Industries, University of Maroua, Kaélé, Cameroon.
  • Clément S; Department of Chemistry, Faculty of science, University of Maroua, Maroua, Cameroon.
  • Emmanuel T; Department of Chemistry, Faculty of science, University of Maroua, Maroua, Cameroon.
  • Laurent S; Department of Chemistry, Faculty of science, University of Ngaoundere, Ngaoundere, Cameroon.
  • Henoumont C; Department of General, Organic and Biomedical Chemistry, Faculty of Medicine and Pharmacy, University of Mons, NMR and Molecular Imaging Laboratory, Mons, Belgium.
  • Venditti A; Department of General, Organic and Biomedical Chemistry, Faculty of Medicine and Pharmacy, University of Mons, NMR and Molecular Imaging Laboratory, Mons, Belgium.
  • Alex De Theodore A; Independent Researcher, Rome, Italy.
  • Benoît L; Department of Organic Chemistry, Faculty of Science, University of Yaoundé I, Yaoundé, Cameroon.
Nat Prod Res ; : 1-6, 2024 Aug 02.
Article em En | MEDLINE | ID: mdl-39092469
ABSTRACT
The phytochemical study of Cordia myxa L. led to the isolation, through chromatographic techniques, of a new triterpenoid saponin, 3-O-[α-L-rhamnopyranosyl-(1→3)-(6-O-acetyl-ß-D-glucopyranosyl)]-22ß-hydroxyolean-12-ene (3) namely Myxaoside A, together with three known compounds, Soyasaponine I (1), oleanolic acid (2), and 3-O-acetyl-oleanolic acid (4). All structures were established, based on 1 & 2D-NMR spectroscopic analysis and comparison with previous published reports. Compound 1-4 were evaluated for their antibacterial activity on various strains of bacteria including Salmonella typhi, Staphylococcus aureus, Pseudomonas aeruginosa, Klebsiella pneumoniae and Vibrio cholerae. It appears that compounds 1 and 3 were active on all the tested microbial species, while compounds 2 and 4, shown no significant effect on S. aureus and K. pneumoniae at low concentrations 6.5 mg/mL and 3.0 mg/mL.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Prod Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Camarões

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Prod Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Camarões