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Merck

08198

Supelco

Eleutheroside E

analytical standard

别名:

[(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

经验公式(希尔记法):
C34H46O18
CAS号:
分子量:
742.72
分類程式碼代碼:
85151701
NACRES:
NA.24

等級

analytical standard

品質等級

化驗

≥98.0% (HPLC)

儲存期限

limited shelf life, expiry date on the label

應用

food and beverages

格式

neat

儲存溫度

2-8°C

SMILES 字串

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-

InChI 密鑰

FFDULTAFAQRACT-RGFZIUCCSA-N

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一般說明

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

應用

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).

包裝

Bottomless glass bottle. Contents are inside inserted fused cone.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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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
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
L B Kardono et al.
Journal of natural products, 53(6), 1447-1455 (1990-11-01)
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Yan-ru Deng et al.
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