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Ternifoliasaponin, a new triterpenoid saponin from the roots of Gardenia ternifolia Schumach & Thonn (Rubiaceae).
Yaya, Hassana; Dabolé, Bernard; Matcheme, Matthieu; Nyemb, Jean Noël; Moussa, Djaouda; Chi, Fru Godloves; Farooq, Rabia; Koubala, Benoît Bargui; Atia, Tul-Wahab; Venditti, Alessandro.
Afiliação
  • Yaya H; Department of Chemistry, Faculty of Science, The University of Maroua, Maroua, Cameroon.
  • Dabolé B; Department of Chemistry, Faculty of Science, The University of Maroua, Maroua, Cameroon.
  • Matcheme M; Department of Refining and Petrochemistry, National Advanced School of Mines and Petroleum Industries, The University of Maroua, Maroua, Cameroon.
  • Nyemb JN; Department of Chemistry, Faculty of Science, The University of Maroua, Maroua, Cameroon.
  • Moussa D; Department of Refining and Petrochemistry, National Advanced School of Mines and Petroleum Industries, The University of Maroua, Maroua, Cameroon.
  • Chi FG; Department of Life and Earth Sciences, Higher Teachers' Training College, The University of Maroua, Maroua, Cameroon.
  • Farooq R; Department of Chemistry, Faculty of Science, University of Buea, Buea, Cameroon.
  • Koubala BB; International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.
  • Atia TW; Department of Chemistry, Faculty of Science, The University of Maroua, Maroua, Cameroon.
  • Venditti A; Department of Life and Earth Sciences, Higher Teachers' Training College, The University of Maroua, Maroua, Cameroon.
Nat Prod Res ; : 1-10, 2023 Nov 10.
Article em En | MEDLINE | ID: mdl-37948554
ABSTRACT
A new triterpenoid saponin, Ternifoliasaponin (1), together with four known compounds (2-5) chikusetsusaponin IVa (2), chikusetsusaponin IVa methyl ester (3), bonushenricoside B (4) and Dianoside C (5) were isolated from roots of Gardenia ternifolia Schumach. & Thonn (Rubiaceae). The structures of isolated compounds were elucidated on the basis of spectroscopic analysis and chemical methods. The antibacterial activities of compounds (3), and (4) were performed by the Muller-Hinton agar diffusion method. The antimicrobial activities of the compounds were studied on Salmonella typhi (Enterobacteriaceae), Staphylococcus aureus and Pseudomonas aeruginosa microorganisms. Compound (3) at 25 mg/mL, showed moderately sensitive effect (8.0 ˂ DIZ ˂14.0 mm) on S. typhi, S. aureus and P. aeruginosa. Compound (4) at 25 mg/mL and compound (3) at 12.5 mg/mL exhibited moderately sensitive effect on S. typhi and S. aureus. Compound (4) inhibited moderately sensitive the S. typhi and P. aeruginosa colonies at 12.5 mg/mL.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article