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Steroidal glycosides from the Vietnamese cultivar Cordyline fruticosa "Fairchild red".
Nguyen, Duc Hung; Mitaine-Offer, Anne-Claire; Miyamoto, Tomofumi; Tanaka, Chiaki; Bellaye, Pierre-Simon; Collin, Bertrand; Chambin, Odile; Lacaille-Dubois, Marie-Aleth.
Afiliação
  • Nguyen DH; PEPITE EA 4267, Laboratoire de Pharmacognosie, UFR des Sciences de Santé, Université de Bourgogne Franche-Comté, BP 87900, 21079, Dijon, Cedex, France; Department of Biology, Thainguyen University of Education, Thainguyen University, 24000, Thainguyen, Viet Nam; Department of Pharmaceutical Technolo
  • Mitaine-Offer AC; PEPITE EA 4267, Laboratoire de Pharmacognosie, UFR des Sciences de Santé, Université de Bourgogne Franche-Comté, BP 87900, 21079, Dijon, Cedex, France. Electronic address: anne-claire.offer@u-bourgogne.fr.
  • Miyamoto T; Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
  • Tanaka C; Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
  • Bellaye PS; Plateforme d'Imagerie et de Radiothérapie Précliniques, Service de Médecine Nucléaire, Centre Georges-François Leclerc, BP77980, 21079, Dijon, Cedex, France.
  • Collin B; Plateforme d'Imagerie et de Radiothérapie Précliniques - ICMUB UMR CNRS 6302, Service de Médecine Nucléaire, Centre Georges-François Leclerc, BP77980, 21079, Dijon, Cedex, France.
  • Chambin O; Department of Pharmaceutical Technology, PAM UMR A 02.102, PCAV Team, Université de Bourgogne Franche-Comté, Dijon, France.
  • Lacaille-Dubois MA; PEPITE EA 4267, Laboratoire de Pharmacognosie, UFR des Sciences de Santé, Université de Bourgogne Franche-Comté, BP 87900, 21079, Dijon, Cedex, France.
Phytochemistry ; 192: 112966, 2021 Dec.
Article em En | MEDLINE | ID: mdl-34624728
ABSTRACT
A phytochemical study of Cordyline fruticosa "Fairchild red" (Asparagaceae) from Vietnam, led to the isolation of fourteen steroidal glycosides, including twelve previously undescribed along with two known ones. Ten compounds were obtained by successive solid/liquid chromatographic methods from an aqueous-ethanolic extract of the roots, and four from the aerial parts. Their structures were elucidated mainly by spectroscopic analysis 2D NMR and mass spectroscopy (ESI-MS), as spirostanol glycosides, 5α-spirost-25(27)-ene-1ß,3ß,4α-triol 1-O-ß-D-fucopyranoside, 5α-spirost-(25)27-ene-1ß,3ß,4α-triol 1-O-ß-D-xylopyranoside, 5α-spirost-(25)27-ene-1ß,3ß,4α-triol 1-O-α-L-rhamnopyranosyl-(1 â†’ 2)-ß-D-fucopyranoside, 5α-spirost-(25)27-ene-1ß,3ß,4α-triol 1-O-α-L-rhamnopyranosyl-(1 â†’ 2)-(4-O-sulfo)-ß-D-fucopyranoside, 5α-spirost-25(27)-ene-1ß,3ß-diol 1-O-α-L-rhamnopyranosyl-(1 â†’ 2)-ß-D-fucopyranoside, and 5α-spirost-25(27)-ene-1ß,3ß-diol 1-O-α-L-rhamnopyranosyl-(1 â†’ 2)-α-L-arabinopyranoside. Furostanol glycosides were also isolated as 26-O-ß-D-glucopyranosyl-5α-furost-(25)27-ene-1ß,3ß,4α,22α,26-pentol 1-O-ß-D-fucopyranoside, 26-O-ß-D-glucopyranosyl-22α-methoxy-5α-furost-(25)27-ene-1ß,3ß,4α,26-tetrol 1-O-ß-D-fucopyranoside, 26-O-ß-D-glucopyranosyl-5α-furost-(25)27-ene-1ß,3ß,22α,26-tetrol 1-O-ß-D-glucopyranoside, 26-O-ß-D-glucopyranosyl-5α-furost-(25)27-ene-1ß,3ß,22α,26-tetrol 1-O-α-L-rhamnopyranosyl-(1 â†’ 2)-ß-D-glucopyranoside, 26-O-ß-D-glucopyranosyl-5α-furost-(25)27-ene-1ß,3ß,22α,26-tetrol 1-O-α-L-rhamnopyranosyl-(1 â†’ 2)-ß-D-fucopyranoside, and 26-O-ß-D-glucopyranosyl-22α-methoxy-5α-furost-(25)27-ene-1ß,3ß,26-triol 1-O-α-L-rhamnopyranosyl-(1 â†’ 2)-ß-D-fucopyranoside. All the isolated compounds were further evaluated for their cytotoxicity against 4T1 cell line, from a mouse mammary gland tissue, using MTS method.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saponinas / Cordyline Limite: Animals / Humans Idioma: En Revista: Phytochemistry Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saponinas / Cordyline Limite: Animals / Humans Idioma: En Revista: Phytochemistry Ano de publicação: 2021 Tipo de documento: Article