Euphol 大戟二烯醇 品牌:Adipogen


Euphol

大戟二烯醇

品牌:Adipogen
CAS No.:514-47-6
储存条件:-20°C
纯度:>98% (HPLC)
产品编号

(生产商编号)

等级 规格 运输包装 零售价(RMB) 库存情况 参考值

AG-CN2-0541-M001

1 mg 720.00


* 干冰运输、大包装及大批量的产品需酌情添加运输费用


* 零售价、促销产品折扣、运输费用、库存情况、产品及包装规格可能因各种原因有所变动,恕不另行通知,确切详情请联系上海金畔生物科技有限公司。

Euphol 大戟二烯醇 品牌:Adipogen


Euphol

大戟二烯醇

品牌:Adipogen
CAS No.:514-47-6
储存条件:-20°C
纯度:>98% (HPLC)
产品编号

(生产商编号)

等级 规格 运输包装 零售价(RMB) 库存情况 参考值

AG-CN2-0541-M005

5 mg 2,160.00


* 干冰运输、大包装及大批量的产品需酌情添加运输费用


* 零售价、促销产品折扣、运输费用、库存情况、产品及包装规格可能因各种原因有所变动,恕不另行通知,确切详情请联系上海金畔生物科技有限公司。

Euphol 大戟二烯醇 品牌:Adipogen


Euphol

大戟二烯醇

品牌:Adipogen
CAS No.:514-47-6
储存条件:-20°C
纯度:>98% (HPLC)
产品编号

(生产商编号)

等级 规格 运输包装 零售价(RMB) 库存情况 参考值

AG-CN2-0541-M025

25 mg 5,760.00


* 干冰运输、大包装及大批量的产品需酌情添加运输费用


* 零售价、促销产品折扣、运输费用、库存情况、产品及包装规格可能因各种原因有所变动,恕不另行通知,确切详情请联系上海金畔生物科技有限公司。

Euphol acetate

上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。

Euphol acetate 

Euphol acetate 是一种三萜烯类化合物,可以从 Euphorbia broteri 中提取得到。Euphol acetate 是肝转运蛋白 OATP1B1/3 的抑制剂。

Euphol acetate

Euphol acetate Chemical Structure

CAS No. : 13879-04-4

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

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生物活性

Euphol acetate is a triterpene that can be isolated from Euphorbia broteri. Euphol acetate is an inhibitor of hepatic transport proteins organic anion-transporting polypeptide 1/3 (OATP1B1/3)[1][2].

IC50 & Target

OATP1B1/3[2]

体外研究
(In Vitro)

Euphol acetate (10 μM) suppresses the uptake of the OATP1B substrate sodium fluorescein in OATP1B1 (29.2%)- or 1B3 (40.2%)-transfected CHO cells[2].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

468.75

Formula

C32H52O2

CAS 号

13879-04-4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. DePascual Teresa, et al. Triterpenes from Euphorbia broteri. Phytochemistry. 1987. 26(6): 1767-1776.

    [2]. Tom De Bruyn, et al. Structure-based identification of OATP1B1/3 inhibitors. Mol Pharmacol. 2013 Jun;83(6):1257-67.

Euphol(Synonyms: 大戟二烯醇)

上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。

Euphol (Synonyms: 大戟二烯醇) 纯度: 98.02%

Euphol 是一种四环三萜醇,是从 Euphorbia tirucalli 的汁液中分离出来的,具有抗炎和免疫调节作用,具有口服活性。 Euphol 通过一种可逆机制抑制单酰基甘油脂肪酶 (MGL) 的活性,IC50=315 nM。 外周 MGL 抑制可调节内源性大麻素系统从而阻止炎症性疼痛的发展。

Euphol(Synonyms: 大戟二烯醇)

Euphol Chemical Structure

CAS No. : 514-47-6

规格 价格 是否有货 数量
5 mg ¥3030 In-stock
10 mg ¥5140 In-stock
50 mg   询价  
100 mg   询价  

* Please select Quantity before adding items.

Euphol 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Immunology/Inflammation Compound Library
  • Metabolism/Protease Compound Library
  • Natural Product Library
  • Human Endogenous Metabolite Compound Library
  • Lipid Compound Library
  • Terpenoids Library
  • Orally Active Compound Library
  • Traditional Chinese Medicine Monomer Library
  • Anti-Cancer Metabolism Compound Library
  • Lipid Metabolism Compound Library
  • Food-Sourced Compound Library

生物活性

Euphol is a tetracyclic triterpene alcohol isolated from the sap of Euphorbia tirucalli with anti-mutagenic, anti-inflammatory and immunomodulatory effects, orally active. Euphol inhibits the monoacylglycerol lipase (MGL) activity via a reversible mechanism (IC50=315 nM). MGL inhibition in the periphery modulates the endocannabinoid system to block the development of inflammatory pain[1].

IC50 & Target

Human Endogenous Metabolite

 

体外研究
(In Vitro)

Euphol (0.01-0.3 mM; 24-72 hours) markedly inhibits T47D cells proliferation, the IC50 values of euphol treatment for 24, 48 and 72 h were 0.26, 0.22 and 0.13 mM, respectively[2].
Euphol (0.03 mM; 48 or 72 hours) leads to cell cycle arrest by regulating expression of cell cycle-associated proteins[2].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Proliferation Assay[2]

Cell Line: T47D cells
Concentration: 0.01, 0.03, 0.1 and 0.3 mM
Incubation Time: 24, 48 and 72 hours
Result: Decreased the percentage of viable cells.

Western Blot Analysis[2]

Cell Line: T47D cells
Concentration: 0.03 mM
Incubation Time: 48 and 72 hours
Result: Increased the expression of p21 and p27, reduced the expression of cyclin A, B1 and D.

分子量

426.72

Formula

C30H50O

CAS 号

514-47-6

中文名称

大戟二烯醇

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶解性数据
In Vitro: 

DMSO : 25 mg/mL (58.59 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.3435 mL 11.7173 mL 23.4346 mL
5 mM 0.4687 mL 2.3435 mL 4.6869 mL
10 mM 0.2343 mL 1.1717 mL 2.3435 mL

*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: 2.5 mg/mL (5.86 mM); Suspended solution; Need ultrasonic

    此方案可获得 2.5 mg/mL (5.86 mM) 的均匀悬浊液,悬浊液可用于口服和腹腔注射。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 2.

    请依序添加每种溶剂: 10% DMSO    90% corn oil

    Solubility: ≥ 2.5 mg/mL (5.86 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (5.86 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在 Shanghai Jinpan Biotech Co Ltd 网站选购。
参考文献
  • [1]. Dutra RC, et al. Euphol, a tetracyclic triterpene produces antinociceptive effects in inflammatory and neuropathic pain: the involvement of cannabinoid system. Neuropharmacology. 2012 Sep;63(4):593-605.

    [2]. Wang L, et al. Euphol arrests breast cancer cells at the G1 phase through the modulation of cyclin D1, p21 and p27 expression. Mol Med Rep. 2013 Oct;8(4):1279-85.