Accéder au contenu
Merck
Toutes les photos(2)

Key Documents

View All Documentation

08198

Supelco

Eleutheroside E

analytical standard

Synonyme(s) :

[(1R,3aR,4S,6aS)-Tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis(2,6-dimethoxy-4,1-phenylene) bis-β-D-glucopyranoside

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
Toutes les photos(2)

About This Item

Formule empirique (notation de Hill):
C34H46O18
Numéro CAS:
39432-56-9
Poids moléculaire :
742.72
Code UNSPSC :
85151701
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥98.0% (HPLC)

Durée de conservation

limited shelf life, expiry date on the label

Application(s)

food and beverages

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

COc1cc(cc(OC)c1O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]3OC[C@@H]4[C@@H]3CO[C@H]4c5cc(OC)c(O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)c(OC)c5

InChI

1S/C34H46O18/c1-43-17-5-13(6-18(44-2)31(17)51-33-27(41)25(39)23(37)21(9-35)49-33)29-15-11-48-30(16(15)12-47-29)14-7-19(45-3)32(20(8-14)46-4)52-34-28(42)26(40)24(38)22(10-36)50-34/h5-8,15-16,21-30,33-42H,9-12H2,1-4H3/t15?,16?,21-,22+,23-,24+,25+,26-,27-,28+,29?,30?,33+,34-

Clé InChI

FFDULTAFAQRACT-RGFZIUCCSA-N

Vous recherchez des produits similaires ? Visite Guide de comparaison des produits

Description générale

Eleutheroside E is one of the major bioactive saponins of Eleutherococcus senticosus.

Application

Eleutheroside E (ELU E) may be used as a reference standard for the analysis of ELU E in:
  • Rat plasma and tissue by solid-phase extraction (SPE) followed by high-performance liquid chromatography (HPLC) and photodiode array detection (PDA).
  • Acanthopanax senticosus by ionic liquids-ultrasound assisted extraction (ILUAE) followed by HPLC with ultraviolet (UV) detection.
  • Eleutherococcus senticosus Maxim. by rapid resolution liquid chromatography (RRLC) equipped with multi-wavelength UV detector.
  • Acanthopanax giraldii Harms by HPLC with diode array detector (DAD).

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
BCCF9712
BCCD0662
BCCB2453
BCBZ8028
BCBW5996

Vous ne trouvez pas la bonne version ?

Si vous avez besoin d'une version particulière, vous pouvez rechercher un certificat spécifique par le numéro de lot.

Rechercher un(e) COA

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Semipreparative separation and determination of eleutheroside E in Acanthopanax giraldii Harms by high-performance liquid chromatography
Wang Z, et al.
Journal of Chromatographic Science, 43(5), 249-252 (2005)
Simultaneous determination of Eleutheroside B and Eleutheroside E in rat plasma by high performance liquid chromatography-electrospray ionization mass spectrometry and its application in a pharmacokinetic study
Ma B, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 917, 84-92 (2013)
Jian-fei Chao et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 31(13), 1078-1080 (2006-10-20)
To investigate the chemical constituents from the branch of Broussonetia papyrifera. Column chromatographic methods were used to isolate the chemical constituents. ESI-MS and NMR methods were employed for their structural elucidation. Six compounds were isolated and identified as (2S)-7, 3'-dihydroxy-4'-methoxyflavan
Chu Van Men et al.
Archives of pharmacal research, 34(12), 2065-2071 (2012-01-03)
A quantitative and pattern recognition analyses were conducted for quality evaluation of Kalopanacis Cortex (KC) using HPLC. For quantitative analysis, four bioactive compounds, liriodendrin, pinoresinol O-β-D-glucopyranoside, acanthoside B and kalopanaxin B, were determined. The analysis method was optimized and validated
Hyun-Ju Jung et al.
Planta medica, 69(7), 610-616 (2003-08-05)
In the present study, liriodendrin isolated by activity-guided fractionation from the ethyl acetate (EtOAc) extracts of the stem bark of Acanthopanax senticosus, was evaluated for anti-inflammatory and antinociceptive activities. Liriodendrin (5, 10 mg/kg/day, p. o.) significantly inhibited the increase of
Afficher tous les articles scientifiques apparentés

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique