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Ginsenoside Ro (Alias: Polysciasaponin P3, Chikusetsusaponin V, Chikusetsusaponin 5)

Catalog No. T3915 Copy Product Info
Purity: 99.66%
🥰Excellent
Ginsenoside Ro (Chikusetsusaponin V) can reduce TXA2 production, weakly reduce COX-1 and TXAS activities, and has antiplatelet effects as a Ca2+ antagonist with an IC50 of 155 μM.

Ginsenoside Ro

Copy Product Info
🥰Excellent
Catalog No. T3915
Alias Polysciasaponin P3, Chikusetsusaponin V, Chikusetsusaponin 5

Ginsenoside Ro (Chikusetsusaponin V) can reduce TXA2 production, weakly reduce COX-1 and TXAS activities, and has antiplatelet effects as a Ca2+ antagonist with an IC50 of 155 μM.

Ginsenoside Ro
Cas No. 34367-04-9
Pack SizePriceUSA StockGlobal StockQuantity
5 mg$40In StockIn Stock
10 mg$73In StockIn Stock
25 mg$163In StockIn Stock
50 mg$278In StockIn Stock
100 mg$393-In Stock
200 mg$539-In Stock
1 mL x 10 mM (in DMSO)$77In StockIn Stock
In stock · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.66%
Color:White
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Product Introduction

Ginsenoside Ro AI Summary
Ginsenoside Ro exhibits multiple bioactivities, including inhibiting hyaluronidase, reducing human amyloid beta (1-40) aggregation, and providing hepatoprotective effects. Specifically, it demonstrated an inhibitory effect on hyaluronidase with an IC50 value of 34000.0 nM, using a colorimetric assay involving hyaluronic acid as a substrate. Additionally, it showed 20.1% activity in reducing amyloid beta aggregation at 25 uM over 24 hours, measured via a Th-T fluorescence assay. Furthermore, Ginsenoside Ro exhibited hepatoprotective activity by decreasing the GPT level by 42.0% at a concentration of 1.0 ug/mL in rat hepatocytes exposed to CCl4/GaIN-induced cytotoxicity..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Ginsenoside Ro (Chikusetsusaponin V) can reduce TXA2 production, weakly reduce COX-1 and TXAS activities, and has antiplatelet effects as a Ca2+ antagonist with an IC50 of 155 μM.
Targets&IC50
Ca2+ antagonistic:155 μM
SynonymsPolysciasaponin P3, Chikusetsusaponin V, Chikusetsusaponin 5
Chemical Properties
Molecular Weight957.11
FormulaC48H76O19
Cas No.34367-04-9
SmilesCC1(C)CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O[C@@H]6O[C@@H]([C@@H](O)[C@H](O)[C@H]6O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)C(O)=O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2C1)C(=O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Relative Density.1.44g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 245 mg/mL (255.98 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (2.09 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.0448 mL5.2241 mL10.4481 mL52.2406 mL
5 mM0.2090 mL1.0448 mL2.0896 mL10.4481 mL
10 mM0.1045 mL0.5224 mL1.0448 mL5.2241 mL
20 mM0.0522 mL0.2612 mL0.5224 mL2.6120 mL
50 mM0.0209 mL0.1045 mL0.2090 mL1.0448 mL
100 mM0.0104 mL0.0522 mL0.1045 mL0.5224 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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