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Ginsenoside Rg3

Product Name
Ginsenoside Rg3
CAS No.
14197-60-5
Chemical Name
Ginsenoside Rg3
Synonyms
Rg3;CS-1328;gensenoside RG3;GINSENOSIDE RG3;opyransoyl)oxy)-;(20S)-PROPANAXADIOL;20S-Ginseniside Rg3;GINSENOSIDE Rg3(SH);Ginsenosides rg3(s);Ginsenoside Rg3 (S-)
CBNumber
CB9713141
Molecular Formula
C42H72O13
Formula Weight
785.01
MOL File
14197-60-5.mol
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Ginsenoside Rg3 Property

Melting point:
315-318°C
Boiling point:
885.0±65.0 °C(Predicted)
Density 
1.30
storage temp. 
2-8°C
solubility 
DMSO: ≥5mg/mL
pka
12.85±0.70(Predicted)
form 
powder
color 
white to beige
optical activity
[α]/D +10 to +20°, c = 1 in methanol
InChIKey
RWXIFXNRCLMQCD-JBVRGBGGSA-N
CAS DataBase Reference
14197-60-5(CAS DataBase Reference)
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Safety

Hazard Codes 
Xn
Risk Statements 
22
WGK Germany 
3
RTECS 
LY9537300
HS Code 
29389090
Toxicity
mouse,LD50,intraperitoneal,1250mg/kg (1250mg/kg),Arzneimittel-Forschung. Drug Research. Vol. 25, Pg. 343, 1975.
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML0184
Product name
Ginsenoside Rg3
Purity
≥98% (HPLC)
Packaging
5mg
Price
$132
Updated
2025/07/31
Sigma-Aldrich
Product number
64139
Product name
Ginsenoside Rg3
Purity
analytical standard
Packaging
10mg
Price
$408
Updated
2025/07/31
TCI Chemical
Product number
G0568
Product name
20(S)-Ginsenoside Rg3
Packaging
10MG
Price
$68
Updated
2025/07/31
Cayman Chemical
Product number
15332
Product name
Ginsenoside Rg3
Purity
≥95%
Packaging
5mg
Price
$32
Updated
2024/03/01
Cayman Chemical
Product number
15332
Product name
Ginsenoside Rg3
Purity
≥95%
Packaging
10mg
Price
$57
Updated
2024/03/01
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Ginsenoside Rg3 Chemical Properties,Usage,Production

Description

Ginsenosides are pharmacologically active natural constituents of ginseng and other plants of the genus Panax. Structurally, they are steroid glycosides derived from the triterpene squalene. Ginsenoside Rg3 is a panaxadiol found in white and red P. ginseng. This ginsenoside has diverse in vitro and in vivo effects, including anti-cancer, neuroprotective, anti-hypertensive, and anti-inflammatory actions. Ginsenoside Rg3 induces apoptosis and inhibits angiogenesis in a variety of cancer models. Notably, this ginsenoside can be produced by heating other ginsenosides, leading to elevated levels in steamed or dried ginseng preparations.

Chemical Properties

White crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from ginseng.

Uses

Ginsenoside Rg3 has been used to investigate its modulatory effects on delayed rectifier potassium current (IKr) channels in long QT syndrome (LQTS)2-human induced pluripotent stem cells (hiPSC-CMs).

Uses

Ginsenoside Rg3 shows a synergistic antitumor effect with cisplatin in cisplatin-resistant bladder tumor cell lines and is considered to be an anti-tumor agent.

Definition

ChEBI: (20S)-ginsenoside Rg3 is a ginsenoside found in Panax ginseng and Panax japonicus var. major that is dammarane which is substituted by hydroxy groups at the 3beta, 12beta and 20 pro-S positions, in which the hydroxy group at position 3 has been converted to the corresponding beta-D-glucopyranosyl-beta-D-glucopyranoside, and in which a double bond has been introduced at the 24-25 position. It has a role as an apoptosis inducer, an antineoplastic agent, a plant metabolite and an angiogenesis modulating agent. It is a ginsenoside, a tetracyclic triterpenoid and a glycoside. It is functionally related to a (20S)-protopanaxadiol. It derives from a hydride of a dammarane.

Biochem/physiol Actions

Ginsenoside Rg3 is a natural product isolated from Panax ginseng. Similar to other ginsenosides it exhibits cardio protective effects. Ginsenoside Rg3 enhances cardiac, hERG (IKr) and KCNQ (Iks), channel currents by interaction with the channel pore entryway. It also inhibits the palmitate-induced apoptosis of MIN6N8 mouse insulinoma beta-cells through modulating p44/42 MAPK activation. Ginsenoside Rg3 increases the level of the transcription factor Nrf2 and induces the mRNA levels of multidrug resistance-associated protein (Mrp) 1 and Mrp3. Rg3 modulate neuroinflammation by attenuating the activation of microglia in response to systemic LPS treatment. It activates AMPK in HepG2 cells and reduces the lipid accumulation thereby decreasing the risk of cardiovascular disease due to dyslipidemia.

Synthesis

52705-93-8

38243-03-7

14197-60-5

1. Accurately weigh 10 mg of ginsenoside Rd and dispense into five 2 mL cold sterile vials and seal (using screw plugs and silica gel rings). 2. Place the vials containing the sample in a 125 ml glass bottle. 3. Place the above glass vials in a sterilizer (SANYO autoclave, model MLS-3780) and steam treat at 120°C for 2 hours at a pressure of 0.13-0.15 MPa. 4. After 2 hours, one of the samples was removed and the rest of the samples were continued to be steam treated under the same temperature and pressure conditions. 5. The above steps were repeated and the samples were removed at 2 h, 4 h, 6 h, 8 h and 10 h to obtain the treatment products at different time points. 6. Ginsenosides Rd, Rg3-S and Rg3-R were analyzed using HPLC and the results were recorded in Table 2.

in vivo

Ginsenoside Rg3 ((20S)-Rg3) is an Aβ-lowering Natural Compound. APP/PS1 mice are treated with Ginsenoside Rg3 once a day for 4 weeks by intraperitoneal injection (10 mg/kg/day). Aβ ELISA analysis of brain tissues reveal that Ginsenoside Rg3 treatment results in a significant reduction of Aβ40 and Aβ42 in the brain[4].

IC 50

Na+ channel: 32.2 μM (IC50); hKv1.4 channel: 32.6 μM (IC50); p65; COX-2; Aβ40; Aβ42

References

[1] Patent: KR2018/76498, 2018, A. Location in patent: Paragraph 0029; 0031-0043

Ginsenoside Rg3 Preparation Products And Raw materials

Raw materials

Preparation Products

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Ginsenoside Rg3 Suppliers

Bontac Bio-engineering (Shenzhen) Co., Ltd.
Tel
0755-+86-0755-27212902 18025386762
Email
marketing@bontac-bio.com
Country
China
ProdList
28
Advantage
60
Wuhan ChemFaces Biochemical Co., Ltd.
Tel
18607101326 15172504745
Fax
+86-27-84254680
Email
aileen@chemfaces.com
Country
China
ProdList
6905
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55
Weifang Huazhi Biological Technology Co., Ltd.
Tel
025-84430028 13815430202
Email
sale02@cqherb.com
Country
China
ProdList
47
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58
Chengdu Biopurify Phytochemicals Ltd.
Tel
+86-028-82633397 18982077548
Fax
+86-28-82633165
Email
cwb1@biopurify.cn
Country
China
ProdList
2376
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60
Hubei CuiRan Biotechnology Co., Ltd.
Tel
00-1816279-5156 18162795156
Email
3391961471@qq.com
Country
China
ProdList
4332
Advantage
58
Shanghai Winherb Medical Technology Co., Ltd.
Tel
021-38218169 13341702378
Fax
QQ:190129269
Email
winherb@126.com
Country
China
ProdList
1245
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58
Chembest Research Laboratories Limited
Tel
+86-21-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6003
Advantage
61
Beijing HwrkChemical Technology Co., Ltd
Tel
18515581800 18501085097
Fax
010-89508210
Email
sales.bj@hwrkchemical.com
Country
China
ProdList
9400
Advantage
55
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
chenyj@titansci.com
Country
China
ProdList
14101
Advantage
59
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18729
Advantage
57
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View Lastest Price from Ginsenoside Rg3 manufacturers

Shaanxi Xianhe Biotech Co., Ltd
Product
GINSENOSIDE Rg3 14197-60-5
Price
US $0.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
1000kg
Release date
2025-04-29
Hebei Zhuanglai Chemical Trading Co Ltd
Product
Ginsenoside Rg3 14197-60-5
Price
US $150.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
500kg
Release date
2024-12-10
Shaanxi Haibo Biotechnology Co., Ltd
Product
Ginsenoside Rg3 14197-60-5
Price
US $0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
2000ton
Release date
2023-08-21

14197-60-5, Ginsenoside Rg3Related Search:


  • beta-d-glucopyranoside,(3-beta,12-beta)-12,20-dihydroxydammar-24-en-3-yl2-o-b
  • dammar-24-ene-12-beta,20-diol,3-beta-((2-o-beta-d-glucopyranosyl-beta-d-gluc
  • eta-d-glucopyranosyl-
  • gensenoside RG3
  • (3β,12β)-12,20-Dihydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside
  • Rg3
  • (2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-DIHYDROXY-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-HYDROXY-17-[(2S)-2-HYDROXY-6-METHYLHEPT-5-EN-2-YL]-4,4,8,10,14-PENTAMETHYL-2,3,5,6,7,9,11,12,13,15,16,17-DODECAHYDRO-1H-CYCLOPENTA[A]PHENANTHREN-3-YL]OXY]-6-(HYDROXYMETHYL)OXAN-3-YL]OXY-6-(HYDROXYMETHYL)OXANE-3,4,5-TRIOL
  • Ginsenoside Rg3, 98%, from Panax ginseng C. A. Mey.
  • (11019-45-7) ginsenoside rg3
  • Ginsenoside Rg3, ≥98%(HPLC)
  • 2-[[4,5-dihydroxy-2-[[12-hydroxy-17-(2-hydroxy-6-methylhept-5-en-2-yl)-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)-3-oxany
  • GINSENOSIDE RG3
  • CS-1328
  • Ginsenoside RG3 Natural Plant Extracts HPLC 15% 50% 98% 14197-60-5
  • opyransoyl)oxy)-
  • 20(s)-ginsenoside-rg3
  • (20S)-PROPANAXADIOL
  • Dammar-24-ene-12β,20-diol, 3β-[(2-O-β-D-
  • glucopyranosyl-β-D-glucopyranosyl)oxy]-
  • Ginsenoside 20(s)-Rg3
  • (20S)-3β-[[2-O-(β-D-Glucopyranosyl)-β-D-glucopyranosyl]oxy]dammarane-24-ene-12β,20-diol
  • 12β,20-Dihydroxy-5α-dammar-24-en-3β-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside
  • 20S-Ginseniside Rg3
  • Ginsenoside Rg3 (S-)
  • (3beta,12beta)-12,20-dihydroxydammar-24-en-3-yl 2-o-beta-d-glucopyranosyl-beta-d-glucopyranoside
  • GINSENOSIDE RG3(S-FORM)(P)
  • GINSENOSIDE Rg3(SH)
  • Ginsenoside Rg3 ,98%
  • Monomer Ginsenoside Rg3
  • Ginsenoside Rg3 (S-Form)
  • β-D-Glucopyranoside, (3β,12β)-12,20-dihydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-
  • (2S,3R,4S,5S,6R)-2-(((2R,3R,4S,5S,6R)-4,5-Dihydroxy-2-(((3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-17-((S)-2-hydroxy-6-methylhept-5-en-2-yl)-4,4,8,10,14-pentamethylhexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
  • Ginsenosides rg3(s)
  • Ginsenoside S type Rg3
  • Ginsenoside Rg3(S-Form)(AS)
  • 20(S)-Ginsenoside Rg3, 10 mM in DMSO
  • 14197-60-5
  • C42H72O11
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
  • Ginsenoside series
  • Saponins
  • The group of Ginsenosides