1. Membrane Transporter/Ion Channel Immunology/Inflammation NF-κB Autophagy Anti-infection
  2. Na+/K+ ATPase IRAK NF-κB Autophagy Mitophagy HSV
  3. Ginsenoside Rb1

Ginsenoside Rb1  (Synonyms: 人参皂苷 Rb1; Gypenoside III)

目录号: HY-N0039 纯度: 98.75%
COA 产品使用指南

Ginsenoside Rb1 是中药人参的成分。Ginsenoside 抑制 Na+, K+-ATPase 活性,IC50 为 6.3±1.0 μM。Ginsenoside Rb1 也抑制 IRAK-1 激活及 NF-κB p65 的磷酸化。

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Ginsenoside Rb1 Chemical Structure

Ginsenoside Rb1 Chemical Structure

CAS No. : 41753-43-9

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10 mM * 1 mL in DMSO ¥732
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1 mg ¥200
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5 mg ¥400
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10 mg ¥600
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25 mg ¥998
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100 mg ¥2400
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Other Forms of Ginsenoside Rb1:

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  • 生物活性

  • 实验参考方法

  • 纯度 & 产品资料

  • 参考文献

生物活性

Ginsenoside Rb1, a main constituent of the root of Panax ginseng, inhibits Na+, K+-ATPase activity with an IC50 of 6.3±1.0 μM. Ginsenoside also inhibits IRAK-1 activation and phosphorylation of NF-κB p65 .

IC50 & Target[1][2][3][6]

Na+, K+-ATPase

6.3 μM (IC50)

IRAK-1

 

p65

 

Autophagy

 

Mitophagy

 

HSV-1

 

体外研究
(In Vitro)

大鼠脑微粒体 Na+,K+-ATPase 活性被 Ginsenoside Rb1 显著且迅速地抑制。Ginsenoside Rb1 对 Na+,K+-ATPase 的 IC50 为 6.3±1.0 μM。随着人参皂苷 Rb1 浓度的增加或 Na+ 和 K+ 浓度的降低,抑制作用增强。
动力学分析表明,人参皂苷是一种非竞争性 ATP 抑制剂[1]。人参皂苷 Rb1 显著抑制白细胞介素 1 受体相关激酶 1 (IRAK-1)、IKK-β、NF-κB 和 MAP 激酶 (ERK、JNK 和 p-38) 的激活;然而,LPS 与 Toll 样受体 4 之间的相互作用、IRAK-4 激活和 IRAK-2 激活不受影响[2]
Ginsenoside Rb1 是中药 Panax ginseng 的成分。Ginsenoside Rb1 是调节孕烷 X 受体 (PXR)/NF-κB 信号传导的主要生物活性化合物。Ginsenoside Rb1 是人参皂苷提取物 (GSE) 中具有强效抗炎活性的化合物。Ginsenoside Rb1 (10 μM) 的浓度根据初步研究进行了优化,以确保足够的抗炎活性并且没有明显的细胞毒性。Ginsenoside Rb1 显著降低 TNF-α 诱导的 IL-1β 和 iNOS mRNA 水平上调,并恢复 LS174T 细胞中 PXR 和 CYP3A4mRNA 水平。TNF-α 导致 PXR 蛋白水平显著降低和磷酸化与总 NF-κB p65 的比例增加,这两者都被 Ginsenoside Rb1 显著消除[3]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

30 mg/kg 和 60 mg/kg 两种剂量的 Ginsenoside Rb1 显著减轻组织学肺损伤。30 mg/kg 和 60 mg/kg 剂量的 Ginsenoside Rb1 均可显著减轻组织学肠损伤[4]。Ginsenoside Rb1 (Rb1) 是中药 Panax ginseng 的一种成分,对脂多糖 (LPS) 诱导的肠系膜微血管高通透性及其潜在机制具有有益作用。在一些大鼠中,Ginsenoside Rb1 (每小时 5 mg/kg) 在 LPS 输注后 30 分钟通过左颈静脉给药。Ginsenoside Rb1 减少微血管内皮细胞中的小窝数量。Ginsenoside Rb1 改善内毒素血症发作后的微血管通透性过高,并通过抑制小窝形成和连接破坏来改善肠水肿,这与抑制 NF-κBSrc 激活有关[5]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

1109.29

Formula

C54H92O23

CAS 号
性状

固体

颜色

White to off-white

中文名称

人参皂苷 Rb1

结构分类
初始来源
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
溶解性数据
细胞实验: 

DMSO 中的溶解度 : 100 mg/mL (90.15 mM; 超声助溶; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

H2O 中的溶解度 : ≥ 33.33 mg/mL (30.05 mM)

* "≥" means soluble, but saturation unknown.

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 0.9015 mL 4.5074 mL 9.0148 mL
5 mM 0.1803 mL 0.9015 mL 1.8030 mL
查看完整储备液配制表

* 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。-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。

* 备注:如您选择水作为储备液,请稀释至工作液后,再用 0.22 μm 的滤膜过滤除菌后使用。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量
=
浓度
×
体积
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物实验:

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

  • 方案 一

    请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 2.5 mg/mL (2.25 mM); 澄清溶液

    此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液。

    1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;再向上述体系中加入 50 μL Tween-80,混合均匀;然后再继续加入 450 μL 生理盐水 定容至 1 mL

    生理盐水的配制:将 0.9 g 氯化钠,溶解于 ddH₂O 并定容至 100 mL,可以得到澄清透明的生理盐水溶液。
  • 方案 二

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

    Solubility: ≥ 2.5 mg/mL (2.25 mM); 澄清溶液

    此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液。

    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。

    20% SBE-β-CD in Saline 的配制(4°C,储存一周):2 g SBE-β-CD(磺丁基醚 β-环糊精)粉末定容于 10 mL 的生理盐水中,完全溶解至澄清透明。
动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
该产品水溶性佳,请具体参考实测 水 / PBS / Saline 中的溶解度数据。
您所需的储备液浓度超过该产品的实测溶解度,如有需要,请与 MCE 中国技术支持联系。
纯度 & 产品资料

纯度: 98.75%

参考文献
Cell Assay
[3]

LS174T cells are seeded in cell imaging dish. After overnight incubation, cells are treated with GSE (100 μg/mL), Ginsenoside Rb1 (10 μM), or CK (10 μM) for 3 hours, followed by an additional incubation with or without TNF-α (20 ng/ml) for 6 hours. At the end of the incubation, cells are harvested and fixed with 4% paraformaldehyde solution at 20°C for 20 minutes. After washing in PBS, cells are permeabilized with 0.2% Triton X-100 in PBS at room temperature for 5 minutes. After incubation in blocking buffer containing 0.1% Triton X-100 and 5% bovine serum albumin, cells are incubated with rabbit NF-κB p65 antibody at 4°C overnight and then with Alexa Fluor 488-conjugated anti-rabbit IgG antibody at room temperature for 30 minutes in 1% bovine serum albumin in PBS. Fluorescence photographs are obtained using a Zeiss 710 confocal microscope[3].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Administration
[4][5]

Mice[4]
Male C57BL/6 mice (9-12 weeks old; 17-22 g) are randomly allocated into eight groups (n=8 in each group): (1) Sham surgical preparation including isolation of the superior mesenteric artery (SMA) without occlusion is performed (Sham); (2) mice are subjected to II/R without treatment (II/R); (3) mice are subjected to II/R with treatment of normal saline 10 minutes before reperfusion (II/R+NS); (4), (5) mice are treated with 30 mg/kg (II/R+Rb1-30) or 60 mg/kg (II/R+Rb1-60) Ginsenoside Rb1, in which surgery is performed as in the II/R group with administration of the Ginsenoside Rb1 intraperitoneally 10 minutes before reperfusion; (6) mice are subjected to Sham surgery and treated with ATRA (ATRA+Sham), which is the inhibitor of Nrf2/ARE signaling pathway; (7) mice are subjected to II/R and treated with ATRA (ATRA+II/R); (8) mice are subjected to II/R and treated with ATRA and 60 mg/kg Ginsenoside Rb1 as group 5 (ATRA+II/R+Rb1-60). During the last two weeks before the operation, the mice in the group 6, 7, 8 receive ATRA i.p. daily at 10 mg/kg and fed on a vitamin A-deficient diet, and the mice in the other groups receive the equivalent volume of corn oil and fed on a control normal diet.
Rats[5]
Male Wistar rats weighing 200-250 g are used. The rats are randomly divided into four groups, 26 animals in each. After being anesthetized with urethane (2 g/kg body wt im), the left femoral vein and left jugular vein of the rat are cannulated. In the LPS group, LPS solution in saline is infused (5 mg/kg per hour) for 90 min via the left femoral vein. The vehicle, instead of LPS solution, is administrated in Sham and Ginsenoside Rb1 alone (Rb1, 5 mg/kg) groups. In the Rb1 posttreatment (LPS+Rb1) group, Ginsenoside Rb1 solution is infused continuously through the left jugular vein 30 min after LPS administration at the dose of 5 mg/kg. Ginsenoside Rb1 solution and the same volume of saline are infused in Ginsenoside Rb1 and Sham groups, respectively, without subsequent LPS administration. In a separate set of experiments, the rats are anesthetized with 2% penobarbital sodium (60 mg/kg body wt ip), and saline, LPS, and Ginsenoside Rb1. After recovery from anesthesia, the animals are allowed access to water and rodent chow, and survival rate is recorded over time until 4 days after LPS stimulation.

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

参考文献

完整储备液配制表

* 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。-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。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
H2O / DMSO 1 mM 0.9015 mL 4.5074 mL 9.0148 mL 22.5369 mL
5 mM 0.1803 mL 0.9015 mL 1.8030 mL 4.5074 mL
10 mM 0.0901 mL 0.4507 mL 0.9015 mL 2.2537 mL
15 mM 0.0601 mL 0.3005 mL 0.6010 mL 1.5025 mL
20 mM 0.0451 mL 0.2254 mL 0.4507 mL 1.1268 mL
25 mM 0.0361 mL 0.1803 mL 0.3606 mL 0.9015 mL
30 mM 0.0300 mL 0.1502 mL 0.3005 mL 0.7512 mL
DMSO 40 mM 0.0225 mL 0.1127 mL 0.2254 mL 0.5634 mL
50 mM 0.0180 mL 0.0901 mL 0.1803 mL 0.4507 mL
60 mM 0.0150 mL 0.0751 mL 0.1502 mL 0.3756 mL
80 mM 0.0113 mL 0.0563 mL 0.1127 mL 0.2817 mL

* 备注:如您选择水作为储备液,请稀释至工作液后,再用 0.22 μm 的滤膜过滤除菌后使用。

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目录号:
HY-N0039
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