GLPBio

Eleutheroside E

Catalog No.: GN10300Purity:>98.00%Synonyms: Syringin E
Eleutheroside E (EE) is a principal active component of Acanthopanax senticosus that possesses anti-fatigue, neuroprotective and immunomodulatory activities.

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Eleutheroside E
Cas No.: 39432-56-9
10mM (in 1mL DMSO)In Stock
$27.00
1
5mgIn Stock
$17.00
1
10mgIn Stock
$25.00
1
25mgIn Stock
$50.00
1
50mgIn Stock
$88.00
1
100mgIn Stock
$140.00
1

Citations

1 publicationsPublications from researchers using this product
IF 11

Description

Eleutheroside E (EE) is a principal active component of Acanthopanax senticosus that possesses anti-fatigue, neuroprotective and immunomodulatory activities[1].

In vitro, Eleutheroside E (100, 300 and 500μM; 48h) can improve the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) -induced apoptosis of PC-12 cells by increasing the mitochondrial membrane potential and reducing the level of intracellular reactive oxygen species (ROS)[2]. Eleutheroside E (25μM; 72h) inhibited the cell viability with promoted apoptosis in Cervical cancer (CC) cells[3]. Eleutheroside E (30, 60 and 100mM; 12h) administration attenuated the cardiomyocyte apoptosis induced by hypoxia-reoxygenation (H/R) injury[4].

In vivo, Pre-treatment with Eleutheroside E (50 and 100 mg/kg; 3 days; i.p.) can improve the pathological manifestations of high-altitude pulmonary edema (HAPE), such as alveolar hemorrhage, thickening of the alveolar walls, inflammatory cell infiltration, and alveolar and interstitial edema, with the effects being positively related to the dose[1]. Supplementation with Eleutheroside E (50 mg/kg/d; 4 weeks) can prevent radiation-induced cognitive impairment and damage of neuron morphology and ultrastructures in the hippocampus of mice[5]. Eleutheroside E (10mg/kg; 20 days; gavage) alleviates cerebral ischemia-reperfusion injury in a 5-hydroxytryptamine receptor 2C (Htr2c)-dependent manner in rats[6].

References:
[1] Shen Z, Huang D, Jia N, Zhao S, Pei C, Wang Y, Wu Y, Wang X, Shi S, Wang F, He Y, Wang Z. Protective effects of Eleutheroside E against high-altitude pulmonary edema by inhibiting NLRP3 inflammasome-mediated pyroptosis. Biomed Pharmacother. 2023 Nov;167:115607.
[2] Yao Y, Liao C, Qiu H, Liang L, Zheng W, Wu L, Meng F. Effect of Eleutheroside E on an MPTP-Induced Parkinson's Disease Cell Model and Its Mechanism. Molecules. 2023 Apr 29;28(9):3820.
[3] Cai Y, Zhang J, Xin T, Xu S, Liu X, Gao Y, Huang H. Eleutheroside E functions as anti-cervical cancer drug by inhibiting the phosphatidylinositol 3-kinase pathway and reprogramming the metabolic responses. J Pharm Pharmacol. 2022 Sep 1;74(9):1251-1260.
[4] Wang S, Yang X. Eleutheroside E decreases oxidative stress and NF-κB activation and reprograms the metabolic response against hypoxia-reoxygenation injury in H9c2 cells. Int Immunopharmacol. 2020 Jul;84:106513.
[5] Song C, Duan F, Ju T, Qin Y, Zeng D, Shan S, Shi Y, Zhang Y, Lu W. Eleutheroside E supplementation prevents radiation-induced cognitive impairment and activates PKA signaling via gut microbiota. Commun Biol. 2022 Jul 8;5(1):680.
[6] Liu Z, Gao W, Xu Y. Eleutheroside E alleviates cerebral ischemia-reperfusion injury in a 5-hydroxytryptamine receptor 2C (Htr2c)-dependent manner in rats. Bioengineered. 2022 May;13(5):11718-11731.

Protocol

Cell experiment [1]:

Cell lines

Hela and SiHa

Preparation Method

After being administered with 0 and 25µM Eleutheroside E, Hela and SiHa cells were collected, washed with phosphate-buffered saline (PBS), resuspended by 0.5ml of bind buffer, and stained with 5µl propidium iodide (PI) and 5µl Annexin V/FITC at room temperature for 15min. The cell apoptosis was analysed on a FACScan flow cytometry using CellQuest software.

Reaction Conditions

25μM; 72h

Applications

Eleutheroside E inhibited the cell viability with promoted apoptosis in Cervical cancer (CC) cells.
Animal experiment [2]:

Animal models

male Sprague-Dawley rats; 100–110g; 4–5 weeks

Preparation Method

The all 42 rats were divided into the following six groups (n = 7) in a manner of random number table: (1) Sham, (2) Eleutheroside E, (3) HAPE, (4) Eleutheroside E 50mg/kg + HAPE, (5) Eleutheroside E 100mg/kg + HAPE and (6) Eleutheroside E 100mg/kg + Nig 4mg/kg + HAPE groups. Rats in the Sham and HAPE groups were treated with normal saline intraperitoneal injections, whereas those in the other four groups were injected intraperitoneally with corresponding doses of Eleutheroside E for 3 days. Nig, an activator of NLRP3, was used to explore the efficacy of Eleutheroside E on NLRP3-mediated pyroptosis in HAPE. Rats in the (6) group were injected intraperitoneally with Nig 30min before the last dose of Eleutheroside E.

Dosage form

50 and 100mg/mice; 3 days; i.p.

Applications

Pre-treatment with Eleutheroside E (50 and 100 mg/kg; 3 days; i.p.) can improve the pathological manifestations of high-altitude pulmonary edema (HAPE), such as alveolar hemorrhage, thickening of the alveolar walls, inflammatory cell infiltration, and alveolar and interstitial edema, with the effects being positively related to the dose.

References:
[1] Cai Y, Zhang J, Xin T, Xu S, Liu X, Gao Y, Huang H. Eleutheroside E functions as anti-cervical cancer drug by inhibiting the phosphatidylinositol 3-kinase pathway and reprogramming the metabolic responses. J Pharm Pharmacol. 2022 Sep 1;74(9):1251-1260.
[2] Shen Z, Huang D, Jia N, Zhao S, Pei C, Wang Y, Wu Y, Wang X, Shi S, Wang F, He Y, Wang Z. Protective effects of Eleutheroside E against high-altitude pulmonary edema by inhibiting NLRP3 inflammasome-mediated pyroptosis. Biomed Pharmacother. 2023 Nov;167:115607.

Product Documents

Purity:>98.00%Appearance:A solid

Chemical Properties

CAS No.
39432-56-9
Synonyms
Syringin E
Chemical Name
(2R,3S,4R,5R,6S)-2-[4-[6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES
COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC
Molecular Formula
C34H46O18
Molecular Weight
742.72
Solubility
≥ 26.2mg/mL in DMSO
Storage
Store at 2-8°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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