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(Synonyms: 人参皂苷 Re; Ginsenoside B2; Panaxoside Re; Sanchinoside Re) 目录号 : GN10307 复制 一键复制产品信息

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。

Ginsenoside Re Chemical Structure

Cas No.:52286-59-6

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10mM (in 1mL DMSO)
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1mg
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5mg
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10mg
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25mg
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Description

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]

实验参考方法

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:
[1] 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.
[2] 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.

化学性质

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
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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
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