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Merck

08198

Supelco

Eleutheroside E

analytical standard

Sinónimos:

[(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

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About This Item

Fórmula empírica (notación de Hill):
C34H46O18
Número de CAS:
Peso molecular:
742.72
Código UNSPSC:
85151701
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

Ensayo

≥98.0% (HPLC)

caducidad

limited shelf life, expiry date on the label

aplicaciones

food and beverages

Formato

neat

temp. de almacenamiento

2-8°C

cadena 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-

Clave InChI

FFDULTAFAQRACT-RGFZIUCCSA-N

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Descripción general

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

Aplicación

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).

Envase

Bottomless glass bottle. Contents are inside inserted fused cone.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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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)
Tomoko Sano et al.
Journal of natural medicines, 64(3), 257-265 (2010-03-11)
Boi and its original plant Sinomenium acutum from Japan were compared with Seifuto and its botanical origins from China in terms of their internal transcribed spacer (ITS) sequences and major chemical components. Boi, Seifuto, and their botanical origins overall showed
D H Kim et al.
Archives of pharmacal research, 22(1), 30-34 (1999-03-11)
When liriodendrin or syringin was incubated for 24 h with human intestinal bacteria, two metabolites, (+)-syringaresinol-beta-D-glucopyranoside and (+)-syringaresinol, from liriodendrin and one metabolite, synapyl alcohol, from syringin were produced. The metabolic time course of liriodendrin was as follows: at early
L B Kardono et al.
Journal of natural products, 53(6), 1447-1455 (1990-11-01)
By bioactivity-directed fractionation, six cytotoxic constituents have been characterized from the bark of Plumeria rubra collected in Indonesia. Three iridoids, fulvoplumierin [1], allamcin [2], and allamandin [3], as well as 2,5-dimethoxy-p-benzoquinone [4], were found to be active constituents of the
Yan-ru Deng et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 30(4), 272-274 (2005-02-24)
To study the chemical constituents from Lamium maculatum var. kansuense. The chemical constituents were isolated and repeatedly purified on silica gel column and the structures were elucidated by the NMR spectra and physico-chemical properties. Six compounds were obtained and identified

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