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Merck
CN

SML0184

人参皂苷 Rg3

≥98% (HPLC), MAPK activation, powder

别名:

(3β, 12β）-12,20-二羟基 dmar-24-烯-3-基 2- O -β- D -吡喃葡萄糖基-β- D -吡喃葡萄糖苷, 20 (S)-人参皂苷-Rg3, Rg3

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关于此项目

经验公式（希尔记法）:
C42H72O13
化学文摘社编号:
14197-60-5
分子量:
785.01
UNSPSC Code:
12352200
PubChem Substance ID:
329825213
NACRES:
NA.77
MDL number:
MFCD06410950
Assay:
≥98% (HPLC)
Form:
powder
Quality level:
100
Storage condition:
desiccated

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产品名称

人参皂苷 Rg3, ≥98% (HPLC)

SMILES string

C\C(C)=C\CC[C@](C)(O)[C@H]1CC[C@]2(C)[C@@H]1[C@H](O)C[C@@H]3[C@@]4(C)CC[C@H](O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)C(C)(C)[C@@H]4CC[C@@]23C

InChI

1S/C42H72O13/c1-21(2)10-9-14-42(8,51)22-11-16-41(7)29(22)23(45)18-27-39(5)15-13-28(38(3,4)26(39)12-17-40(27,41)6)54-37-35(33(49)31(47)25(20-44)53-37)55-36-34(50)32(48)30(46)24(19-43)52-36/h10,22-37,43-51H,9,11-20H2,1-8H3/t22-,23+,24+,25+,26-,27+,28-,29-,30+,31+,32-,33-,34+,35+,36-,37-,39-,40+,41+,42-/m0/s1

InChI key

RWXIFXNRCLMQCD-JBVRGBGGSA-N

assay

≥98% (HPLC)

form

powder

optical activity

[α]/D +10 to +20°, c = 1 in methanol

storage condition

desiccated

color

white to beige

solubility

DMSO: ≥5 mg/mL

storage temp.

2-8°C

Quality Level

100

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相关类别

Application

人参皂苷 Rg3 可能用于细胞信号传导研究。
人参皂苷 Rg3 用于研究其对长QT综合征（LQTS）2-人诱导多能干细胞（hiPSC-CM）中延迟整流钾电流（IKr）通道的调控作用。

Biochem/physiol Actions

人参皂苷 Rg3 是从 人参中分离得到的天然产物 。与其他人参皂甙相似，它具有心脏保护作用。人参皂甙 Rg3 通过与通道孔入口的相互作用增强心脏、hERG (IKr) 和 KCNQ (Iks) 通道电流。它还通过调节 p44/42 MAPK 活化抑制棕榈酸酯诱导的 MIN6N8 小鼠胰岛素瘤 β 细胞凋亡。人参皂苷 Rg3 提高转录因子 Nrf2 的级别，诱导多药耐药相关蛋白 (Mrp) 1 和 Mrp3 的 mRNA 水平。Rg3 通过减弱小胶质细胞对全身 LPS 处理的反应来调节神经炎症。它激活 HepG2 细胞中的 AMPK，减少脂质蓄积，从而降低血脂异常导致的心血管疾病风险。

Features and Benefits

该化合物在受体分类和信号转导手册的钾通道页面上有重点介绍。想要浏览手册的其他页面， 请单击此处。

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000509867
0000509867
0000479226
0000479225
0000479225

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Sang Il Gum et al.
Oxidative medicine and cellular longevity, 2013, 957947-957947 (2013-06-15)
Previously, we found that Korean red ginseng suppressed acetaminophen (APAP)-induced hepatotoxicity via alteration of its metabolic profile involving GSTA2 induction and that ginsenoside Rg3 was a major component of this gene induction. In the present study, therefore, we assessed the
Seohyun Lee et al.
International journal of molecular sciences, 13(5), 5729-5739 (2012-07-04)
Cardiovascular disease (CVD) is one of the main causes of mortality worldwide, and dyslipidemia is a major risk factor for CVD. Ginseng has been widely used in the clinic to treat CVD. Ginsenoside Rg3, one of the major active components
Jian-Wen Jiang et al.
World journal of gastroenterology, 17(31), 3605-3613 (2011-10-12)
To investigate the anti-tumor function of ginsenoside Rg3 on hepatocellular carcinoma (HCC) in vitro and in vivo, and its mechanism. Hep1-6 and HepG2 cells were treated by Rg3 in different concentrations (0, 50, 100 and 200 μg/mL) in vitro. After
Sun-Min Park et al.
Biological & pharmaceutical bulletin, 35(9), 1546-1552 (2012-09-15)
Neuroinflammation, characterized by activation of microglia and expression of major inflammatory mediators, contributes to neuronal damage in addition to acute and chronic central nervous system (CNS) disease progression. The present study investigated the immune modulatory effects of ginsenoside Rg3, a
Xiaojie Wei et al.
International immunology, 24(7), 465-471 (2012-03-20)
Our previous investigation demonstrated that ginsenoside Rg3 was active in promotion of the immune response. In this study, two epimers, 20(R)-Rg3 and 20(S)-Rg3, were compared for their adjuvant effects on the immune response against ovalbumin (OVA). BALB/c mice were immunized
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