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人参皂苷 Re /Ginsenoside Re {[allProObj[0].p_purity_real_show]}

货号:A149220 同义名: 人参皂甙 Re / Panaxoside Re;Ginsenoside B2

Ginsenoside Re is a panaxatriol saponin that has diverse in vitro and in vivo effects, including vasorelaxant, antioxidant, antihyperlipidemic, and angiogenic actions.

Ginsenoside Re 化学结构 CAS号:52286-59-6
Ginsenoside Re 化学结构
CAS号:52286-59-6
Ginsenoside Re 3D分子结构
CAS号:52286-59-6
Ginsenoside Re 化学结构 CAS号:52286-59-6
Ginsenoside Re 3D分子结构 CAS号:52286-59-6
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Ginsenoside Re 纯度/质量文件 产品仅供科研

货号:A149220 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 JNK JNK1 JNK2 JNK3 其他靶点 纯度
Mulberroside A 99%+
Loureirin B Calcium Channel,Potassium Channel 99%+
Ginsenoside Re NF-κB 98%
(+)-(3R,8S)-Falcarindiol STAT,ERK 99%+
trans-Zeatin p38 MAPK,ERK 95+%
Urolithin B ERK,NF-κB 95%
Cucurbitacin IIb NF-κB 98+%
Astragaloside IV mTOR,Akt,NF-κB 98%
NDMC101 99%+
DB07268 ++++

JNK1, IC50: 9 nM

99%+
SP600125 +

MKK4, IC50: 0.4 μM

+++

JNK1, IC50: 40 nM

+++

JNK2, IC50: 40 nM

+++

JNK3, IC50: 90 nM

98%
JNK-IN-7 ++++

JNK1, IC50: 1.5 nM

++++

JNK2, IC50: 2 nM

++++

JNK3, IC50: 0.7 nM

98+%
JNK-IN-8 ++++

JNK1, IC50: 4.7 nM

+++

JNK2, IC50: 18.7 nM

++++

JNK3, IC50: 1 nM

99%+
3,3',5-Triiodo-L-thyronine ++

JNK1, Kd: 240 nM

++

JNK2, Kd: 290 nM

+++

JNK3, Kd: 66 nM

98%
IQ-1S free acid +

JNK1, IC50: 390 nM

++

JNK2, IC50: 360 nM

+++

JNK3, IC50: 87 nM

98%
BI-78D3 ++

JNK, IC50: 280 nM

++

JNK, IC50: 280 nM

++

JNK, IC50: 280 nM

++

JNK, IC50: 280 nM

99%+
Bentamapimod +++

JNK1, IC50: 80 nM

+++

JNK2, IC50: 90 nM

++

JNK3, IC50: 230 nM

98%
Resveratrol +

JNK1, IC50: 50 μM

98%
Indirubin-3′-oxime 99%+
SU3327 +

JNK, IC50: 0.7 μM

+

JNK, IC50: 0.7 μM

+

JNK, IC50: 0.7 μM

+

JNK, IC50: 0.7 μM

99%+
JNK Inhibitor VIII ++++

JNK1, IC50: 45 nM

JNK1, Ki: 2 nM

++++

JNK2, Ki: 4 nM

JNK2, IC50: 160 nM

+++

JNK3, Ki: 52 nM

98%
Doramapimod 99%+
RPI-1 97%
TCS JNK 5a ++

JNK2, pIC50: 6.5

++

JNK3, pIC50: 6.7

98%
SP 600125, negative control +

JNK2, IC50: 18 μM

+

JNK3, IC50: 24 μM

97%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
产品名称 NF-κB 其他靶点 纯度
PDTC ammonium 98%
QNZ ++++

NF-κB, IC50: 11 nM

99%+
Sodium 4-Aminosalicylate Dihydrate 98%
Sodium Salicylate 95%
Parthenolide p53 97% HPLC
JSH-23 +

NF-κB, IC50: 7.1 μM

98%
Phenethyl caffeate 98%
Andrographolide 98+%
Curcumin Nrf2,HDAC 98%
SC75741 +++

NF-κB, EC50: 200 nM

99%+
CBL0137 HCl ++

NF-κB, EC50: 0.47 μM

p53 99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Ginsenoside Re 生物活性

靶点
  • JNK

描述 Ginsenoside Re is an extract from Panax notoginseng. Ginsenoside Re decreased the Aβ(β-amyloid protein) levels in N2a/APP695 cells. Ginsenoside Re decreased the BACE1 (β-site amyloid precursor protein cleaving enzyme 1) mRNA and protein levels and inhibited BACE1 activity in the N2a/APP695 cells. Ginsenoside Re significantly increased the PPARγ protein and mRNA levels[3]. Ginsenoside Re can improve isoproterenol-induced myocardial fibrosis and heart failure by regulation of the TGF-β1(transforming growth factor)/Smad3 pathway[4]. GRe protects MA-induced (methamphetamine) dopaminergic neurotoxicity via upregulatgion of dynorphin-mediated κ-opioid receptor and downregulation of substance P-mediated NK1 R (neurokinin 1 receptor) [5]. Moreover, ginsenoside Re-dependent upregulation of GPX4 (glutathione peroxidase 4) reduces oxidative stress and thereby alleviates 6-OHDA(6-hydroxydopamine)-induced neuronal damage[6]. After GS-Re treatment, the vessel lumen of injured vessels showed significant increases in the GS-Re 25.0 and 50.0 mg/kg/d (intermediate- and high-dose) groups according to H.E. staining. GS-Re can suppress balloon injury-induced vascular neointimal hyperplasia by inhibiting VSMC proliferation[7].

Ginsenoside Re 参考文献

[1]Wang L, Yuan D, et al. Ginsenoside Re Promotes Nerve Regeneration by Facilitating the Proliferation, Differentiation and Migration of Schwann Cells via the ERK- and JNK-Dependent Pathway in Rat Model of Sciatic Nerve Crush Injury. Cell Mol Neurobiol. 2015 Aug;35(6):827-40.

[2]Sukrittanon S, Watanapa WB, Ruamyod K. Ginsenoside Re enhances small-conductance Ca(2+)-activated K(+) current in human coronary artery endothelial cells. Life Sci. 2014 Oct 12;115(1-2):15-21.

[3]Cao G, Su P, Zhang S, et al. Ginsenoside Re reduces Aβ production by activating PPARγ to inhibit BACE1 in N2a/APP695 cells. Eur J Pharmacol. 2016;793:101-108

[4]Wang QW, Yu XF, Xu HL, Zhao XZ, Sui DY. Ginsenoside Re Improves Isoproterenol-Induced Myocardial Fibrosis and Heart Failure in Rats. Evid Based Complement Alternat Med. 2019;2019:3714508. Published 2019 Jan 1

[5]Dang DK, Shin EJ, Kim DJ, et al. Ginsenoside Re protects methamphetamine-induced dopaminergic neurotoxicity in mice via upregulation of dynorphin-mediated κ-opioid receptor and downregulation of substance P-mediated neurokinin 1 receptor. J Neuroinflammation. 2018;15(1):52. Published 2018 Feb 21

[6]Lee GH, Lee WJ, Hur J, Kim E, Lee HG, Seo HG. Ginsenoside Re Mitigates 6-Hydroxydopamine-Induced Oxidative Stress through Upregulation of GPX4. Molecules. 2020;25(1):188. Published 2020 Jan 2

[7]Gao Y, Gao CY, Zhu P, et al. Ginsenoside Re inhibits vascular neointimal hyperplasia in balloon-injured carotid arteries through activating the eNOS/NO/cGMP pathway in rats. Biomed Pharmacother. 2018;106:1091-1097

Ginsenoside Re 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.06mL

0.21mL

0.11mL

5.28mL

1.06mL

0.53mL

10.56mL

2.11mL

1.06mL

Ginsenoside Re 技术信息

CAS号52286-59-6
分子式C48H82O18
分子量 947.154
别名 人参皂甙 Re ;Panaxoside Re;Ginsenoside B2;NSC 308877;Chikusetsusaponin Ivc;Sanchinoside Re
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Inert atmosphere,2-8°C

溶解度

DMSO: 50 mg/mL(52.79 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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