Ginsenoside Re
(Synonyms: 人参皂苷 Re; Ginsenoside B2; Panaxoside Re; Sanchinoside Re) 目录号 : GN10307
Ginsenoside Re是一种存在于Panax ginseng,具有高效抗氧化和抗炎生物活性的天然化合物。
Cas No.:52286-59-6
Sample solution is provided at 25 µL, 10mM.
Ginsenoside Re is a natural compound found in Panax ginseng, possessing potent antioxidant and anti-inflammatory bioactivities[1]. Ginsenoside Re is commonly used in the treatment of cardiovascular diseases (myocardial ischemia, arrhythmia), and is also extensively studied for neuroprotection in Alzheimer's/Parkinson's disease, improvement of metabolic function (diabetes), and promotion of bone regeneration[2,3,4].
In vitro, pretreatment of primary dopaminergic midbrain neurons with Ginsenoside Re (1, 5, 10μM) for 2h, followed by exposure to CCl4 (2.5mM) for 48h, significantly reduced CCl4-induced loss of tyrosine hydroxylase (TH+) positive neurons and preserved neurite length and number[5]. Pretreatment of PC12 cells with Ginsenoside Re (0.1-100μM) for 2h, followed by incubation in serum-free medium for 24-96h, markedly attenuated serum deprivation-induced cytotoxicity and enhanced cell viability[6].
In vivo, administration of Ginsenoside Re (10mg/kg/day) via intraperitoneal injection to ob/ob mice for 12 days resulted in a 17.8% reduction in the area under the curve (AUC) for glucose during an intraperitoneal glucose tolerance test (IPGTT) and significantly improved glucose diposal[7]. Intragastrically of Ginsenoside Re (15mg/kg) to mice for 7 consecutive days, followed by intraperitoneal injection of lipopolysaccharide (LPS; 10mg/kg), significantly increased 24-hour survival rates and prolonged survival time[8].
References:
[1] HUANG Y C, CHEN C T, CHEN S C, et al. A natural compound (ginsenoside Re) isolated from Panax ginseng as a novel angiogenic agent for tissue regeneration[J]. Pharmaceutical Research, 2005, 22(4): 636-646.
[2] KIM J H, YI Y S, KIM M Y, et al. Role of ginsenosides, the main active components of Panax ginseng, in inflammatory responses and diseases[J]. Journal of Ginseng Research, 2017, 41(4): 435-443.
[3] KIM J H. Pharmacological and medical applications of Panax ginseng and ginsenosides: a review for use in cardiovascular diseases[J]. Journal of Ginseng Research, 2018, 42(3): 264-269.
[4] WANG Y, ZHANG G, DENG L, et al. Ginsenoside Re promotes osteogenic differentiation via BMP2/p38 pathway in vivo and in vitro[J]. Journal of Ginseng Research, 2025.
[5] ZHANG X, WANG Y, MA C, et al. Ginsenoside Rd and ginsenoside Re offer neuroprotection in a novel model of Parkinson’s disease[J]. American Journal of Neurodegenerative Disease, 2016, 5(1): 52.
[6] JI Z N, DONG T T X, YE W C, et al. Ginsenoside Re attenuate β-amyloid and serum-free induced neurotoxicity in PC12 cells[J]. Journal of Ethnopharmacology, 2006, 107(1): 48-52.
[7] XIE J T, MEHENDALE S R, LI X, et al. Anti-diabetic effect of ginsenoside Re in ob/ob mice[J]. Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease, 2005, 1740(3): 319-325.
[8] CHEN R C, WANG J, YANG L, et al. Protective effects of ginsenoside Re on lipopolysaccharide-induced cardiac dysfunction in mice[J]. Food & Function, 2016, 7(5): 2278-2287.
Ginsenoside Re是一种存在于Panax ginseng,具有高效抗氧化和抗炎生物活性的天然化合物[1]。Ginsenoside Re通常用于心血管疾病(心肌缺血、心律失常)的治疗,以及阿尔茨海默病/帕金森病神经保护、改善代谢功能(糖尿病)和促进骨骼再生的研究[2,3,4]。
在体外,Ginsenoside Re(1, 5, 10μM)预处理原代中脑多巴胺能神经元2h,再加入CCl4(2.5mM)处理48h,能显著减少CCl4诱导的酪氨酸羟化酶(TH+)阳性神经元丢失,保护神经突长度和数量[5]。Ginsenoside Re(0.1-100μM)预处理PC12细胞2h后,更换为无血清培养基继续培养24-96h,能显著减轻血清剥夺引起的细胞毒性,提高细胞存活率[6]。
在体内,Ginsenoside Re(10mg/kg/day)通过腹腔注射处理ob/ob小鼠12天,在腹腔内葡萄糖耐量测试(IPGTT)中葡萄糖曲线下面积(AUC)较对照组降低17.8%,葡萄糖处理率显著提高[7]。小鼠灌胃Ginsenoside Re(15mg/kg)连续7天,再腹腔注射10mg/kg脂多糖(LPS),能显著提高小鼠24h生存率,延长生存时间[8]。
| Cell experiment [1]: | |
Cell lines | Primary dopaminergic midbrain neuron |
Preparation Method | Primary dopaminergic midbrain neuron were pretreated with 1, 5, and 10μM Ginsenoside Re for 2h and then exposed to 2.5mM CCl4 for 48h. TH+ positive neurons were identified by immunocytochemical staining, and their neurite length, and neurite number were assessed under microscopy. |
Reaction Conditions | 1, 5, and 10μM; 2h |
Applications | Ginsenoside Re treatment significantly reduced CCl4-induced loss of TH+ positive neurons and protected neurite length and number. |
| Animal experiment [2]: | |
Animal models | C57BL/6J ob/ob mice |
Preparation Method | ob/ob mice were administered Ginsenoside Re (10mg/kg) via daily intraperitoneal injection for 12 consecutive days, followed by an intraperitoneal glucose tolerance test (IPGTT) in which glucose (2g/kg) was injected intraperitoneally and blood glucose levels were measured from the tail vein at 0, 30, 60, and 120min. Glucose exposure was evaluated by calculating the AUC for glucose. |
Dosage form | 10mg/kg/day; 12 days; i.p. |
Applications | Treatment with Ginsenoside Re reduced the AUC for glucose by 17.8% compared to the control group, and significantly improved glucose disposal. |
References: | |
| Cas No. | 52286-59-6 | SDF | |
| 别名 | 人参皂苷 Re; Ginsenoside B2; Panaxoside Re; Sanchinoside Re | ||
| 化学名 | Panaxoside RE, Ginsenoside B2, Chikusetsusaponin IVc | ||
| Canonical SMILES | CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CC4(C(CC(C5C4(CCC5C(C)(CCC=C(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C7(C3C(C(CC7)O)(C)C)C)C)CO)O)O)O)O)O | ||
| 分子式 | C48H82O18 | 分子量 | 947.14 |
| 溶解度 | ≥ 43.1mg/mL in DMSO | 储存条件 | Store at 2-8°C, protect from light |
| General tips | 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 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
||
| Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
![]() |
1 mg | 5 mg | 10 mg |
| 1 mM | 1.0558 mL | 5.2791 mL | 10.5581 mL |
| 5 mM | 211.2 μL | 1.0558 mL | 2.1116 mL |
| 10 mM | 105.6 μL | 527.9 μL | 1.0558 mL |
| 第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
| 给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
| 第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
- View current batch:
- Purity: >99.00% Appearance: A solid
- COA (Certificate of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
















