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Merck

90974

Supelco

Eleutheroside B

analytical standard

Sinónimos:

(E)-4-[-3-Hydroxy-1-propenyl]-2,6-dimethoxyphenyl-β-D-glucopyranoside, Ilexanthin A, Ligustrin, Lilacin, Magnolenin, Methoxyconiferine, Sinapyl alcohol 4-O-glucoside, Syringin, Syringoside

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About This Item

Fórmula empírica (notación de Hill):
C17H24O9
Número de CAS:
Peso molecular:
372.37
Beilstein/REAXYS Number:
97166
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

food and beverages

format

neat

storage temp.

2-8°C

SMILES string

COc1cc(\C=C\CO)cc(OC)c1O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O

InChI

1S/C17H24O9/c1-23-10-6-9(4-3-5-18)7-11(24-2)16(10)26-17-15(22)14(21)13(20)12(8-19)25-17/h3-4,6-7,12-15,17-22H,5,8H2,1-2H3/b4-3+/t12-,13-,14+,15-,17+/m1/s1

InChI key

QJVXKWHHAMZTBY-GCPOEHJPSA-N

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General description

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

Application

Eleutheroside B may be used as a reference standard for the analysis of eleutheroside B in:
  • Rat plasma by protein precipitation with methanol and high performance liquid chromatography-electrospray ionization tandem mass spectrometry (HPLC-ESI-MS/MS).
  • Rat tissue samples by solid-phase extraction (SPE) followed by HPLC combined with photodiode array detection (PDA).
  • Acanthopanax senticosus by ionic liquids-ultrasound assisted extraction (ILUAE) followed by HPLC with ultra-violet (UV) detection.
  • Eleutherococcus senticosus Maxim. by rapid resolution liquid chromatography (RRLC) equipped with multi-wavelength UV detector.
  • Acanthopanax sessiliflorus Seem. (ASS) by ultra-performance liquid chromatography-quadrupole-time-of-flight mass spectrometry (UPLC-Q-TOF-MS).

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Visite la Librería de documentos

Yi-Chun Lai et al.
Natural product communications, 8(3), 363-365 (2013-05-18)
Nineteen compounds and an HPLC inseparable mixture, composed of compounds 20 and 21, were isolated from the leaves and twigs of Dendropanax dentiger (Harms ex Diels) Merr. Of these, syringin (1) is the most abundant, 6'-O-apiofuranosyl dendranthemoside A (16) is
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, Biomedical Sciences and Applications, 917, 84-92 (2013)
Yuan-yuan Song et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 45(8), 1006-1011 (2011-03-01)
This study is to investigate the therapeutic effect of syringin on adjuvant arthritis (AA) in rats and its mechanisms. Complete Freund's adjuvant (FCA) was used to induce AA in rats. Secondary paw swelling of AA rats was measured with volume
Fang Lu et al.
Biomedical chromatography : BMC, 26(10), 1269-1275 (2012-01-26)
We elucidated the structure and metabolite profile of eleutheroside B, a component derived from the extract of Acanthopanax senticosus Harms, after oral administration of the extract in rats. Samples of rat plasma were collected and analyzed by selective high-resolution liquid
Ho-Shan Niu et al.
Neuroscience letters, 445(1), 113-116 (2008-09-09)
Syringin is an active principle purified from the rhizome and root parts of Eleutherococcus senticosus (Araliaceae). The present study is designed to clarify the role of sympathetic activation in the insulinotropic effect of syringin. Plasma glucose lowering effect accompanying with

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