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New acylated triterpenoid saponins from the roots of Acacia polyacantha Willd. (Fabaceae).
Atangana, Jean Faustin; Messi, Lin Marcellin; Haddad, Mohamed; Mbing, Joséphine Ngo; Boyogueno Begoude, Aime-Didier; Pegnyemb, Dieudonné Emmanuel; Choudhary, Muhammad Iqbal; Noté, Olivier Placide.
Afiliação
  • Atangana JF; Laboratoire de Pharmacochimie des Substances Naturelles, Département de Chimie Organique, Faculté de Sciences, Université de Yaoundé I, BP 812, Yaoundé, Cameroon; H.E.J Research Institute of Chemistry, International Center for Chemical and Biological Sciences (ICCBS), University of Karachi, Karachi,
  • Messi LM; Laboratoire de Pharmacochimie des Substances Naturelles, Département de Chimie Organique, Faculté de Sciences, Université de Yaoundé I, BP 812, Yaoundé, Cameroon; Institut de Recherche Agricole pour le Développement (IRAD), BP 2067, Yaoundé, Cameroon. Electronic address: linmarcellinmessi@yahoo.fr.
  • Haddad M; UMR 152 Pharma Dev, Université de Toulouse, IRD, UPS, France.
  • Mbing JN; Laboratoire de Pharmacochimie des Substances Naturelles, Département de Chimie Organique, Faculté de Sciences, Université de Yaoundé I, BP 812, Yaoundé, Cameroon.
  • Boyogueno Begoude AD; Institut de Recherche Agricole pour le Développement (IRAD), BP 2067, Yaoundé, Cameroon.
  • Pegnyemb DE; Laboratoire de Pharmacochimie des Substances Naturelles, Département de Chimie Organique, Faculté de Sciences, Université de Yaoundé I, BP 812, Yaoundé, Cameroon.
  • Choudhary MI; H.E.J Research Institute of Chemistry, International Center for Chemical and Biological Sciences (ICCBS), University of Karachi, Karachi, 75270, Pakistan.
  • Noté OP; Laboratoire de Pharmacochimie des Substances Naturelles, Département de Chimie Organique, Faculté de Sciences, Université de Yaoundé I, BP 812, Yaoundé, Cameroon. Electronic address: Oliviernote1@yahoo.fr.
Carbohydr Res ; 523: 108725, 2023 Jan.
Article em En | MEDLINE | ID: mdl-36455425
In our continuing search of saponins from the plants of Fabaceae family, phytochemical investigation of the roots of Acacia polyacantha, led to the isolation and structural characterization of six undescribed triterpenoid saponins, named polyacosides A-F (1-6). Their structures were established, using extensive analysis by NMR techniques, mainly 1D NMR (1H, 13C, and DEPT) and 2D NMR (COSY, NOESY, HSQC, TOCSY and HMBC) experiments, HRESIMS and by comparison with the literature data, as 3-O-[ß-d-xylopyranosyl-(1 â†’ 4)- [ß-d-galactopyranosyl-(1 â†’ 2)-ß-d-xylopyranosyl-(1 â†’ 2)]-α-l-arabinopyranosyl]-21-O-[Cis-2-methoxycinnamoyl] machaerinic acid (1), 3-O-[ß-d-xylopyranosyl-(1 â†’ 4)- [ß-d-galactopyranosyl-(1 â†’ 2)-ß-d-xylopyranosyl-(1 â†’ 2)]-α-l-arabinopyranosyl]-21-O- [Cis-3,4-dimethoxycinnamoyl] machaerinic acid. (2), 3-O- [ß-d-galactopyranosyl-(1 â†’ 2)-ß-d-xylopyranosyl-(1 â†’ 2)-α-l-arabinopyranosyl]-21-O- [Trans-4-methoxycinnamoyl] machaerinic acid (3), 3-O- [ß-d-glucopyranosyl-(1 â†’ 2)-ß-d-glucopyranosyl] -21-O- [Cis-3,4-dimethoxycinnamoyl] machaerinic acid (4), 3-O- [ß-d-glucopyranosyl-(1 â†’ 2)-ß-d-glucopyranosyl] -21-O- [Cis-2-methoxycinnamoyl] machaerinic acid (5) and 3-O- [ß-d-glucopyranosyl-(1 â†’ 2)-ß-d-glucopyranosyl] -21-O- [Trans-4-methoxycinnamoyl] machaerinic acid (6). Our findings highlight the presence of methoxycinnamoyl group linked to C-21 of the machaerinic acid aglycone moiety as first report of 21-methoxycinnamoyl-machaerinic acid derivative from the plants of Acacia genus (Fabaceae). This represents therefore a valuable contribution to the chemotaxonomy of the Acacia genus of Fabaceae family, which is known to be a rich source of triterpenoid saponins.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saponinas / Triterpenos / Acacia Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saponinas / Triterpenos / Acacia Idioma: En Ano de publicação: 2023 Tipo de documento: Article