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(20R)-Protopanaxadiol

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Catalog No. T3S1513Cas No. 7755-01-3
Alias Protopanaxadiol, 20R-Protopanaxadiol, (20R)-Protopanaxdiol

1. (20R)-Protopanaxadiol ((20R)-Protopanaxdiol) has the effect of anti-tumor through increasing the activity of body immunity, inhibiting tumor interstitial microvascular density and its proliferation activity, improving the lymphocyte transformation, the activity of NK cells and the contents of IL-2 significantly. 2. (20R)-Protopanaxadiol prevents and heals obesity, fatty liver and hypertriglyceridemia in mice fed with a high-fat diet.

(20R)-Protopanaxadiol

(20R)-Protopanaxadiol

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Purity: 99.97%
Catalog No. T3S1513Alias Protopanaxadiol, 20R-Protopanaxadiol, (20R)-ProtopanaxdiolCas No. 7755-01-3
1. (20R)-Protopanaxadiol ((20R)-Protopanaxdiol) has the effect of anti-tumor through increasing the activity of body immunity, inhibiting tumor interstitial microvascular density and its proliferation activity, improving the lymphocyte transformation, the activity of NK cells and the contents of IL-2 significantly. 2. (20R)-Protopanaxadiol prevents and heals obesity, fatty liver and hypertriglyceridemia in mice fed with a high-fat diet.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
2 mg$36In StockIn Stock
5 mg$54In StockIn Stock
10 mg$77In StockIn Stock
25 mg$123In StockIn Stock
50 mg$179In Stock-
100 mg$266InquiryInquiry
1 mL x 10 mM (in DMSO)$61In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.97%
Appearance:Solid
Color:White
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Product Introduction

(20R)-Protopanaxadiol AI Summary
(20R)-Protopanaxadiol has been found to exhibit inhibitory activity in an in vitro assay targeting rat liver Acyl coenzyme A:cholesterol acyltransferase, with an IC50 value of 10,000.0 nM. It also demonstrates cytotoxicity against human HL60 and HepG2 cells, with IC50 values of 23,420.0 nM and 69,070.0 nM, respectively, as determined by MTT assay after 48 hours. Additionally, (20R)-Protopanaxadiol shows dose-dependent activation of human CK-MM enzyme activity, achieving the highest increase at 20 µM, although bioactivity decreases at higher concentrations, indicating a potential optimal dosage for maximal enzyme activation..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
1. (20R)-Protopanaxadiol ((20R)-Protopanaxdiol) has the effect of anti-tumor through increasing the activity of body immunity, inhibiting tumor interstitial microvascular density and its proliferation activity, improving the lymphocyte transformation, the activity of NK cells and the contents of IL-2 significantly. 2. (20R)-Protopanaxadiol prevents and heals obesity, fatty liver and hypertriglyceridemia in mice fed with a high-fat diet.
SynonymsProtopanaxadiol, 20R-Protopanaxadiol, (20R)-Protopanaxdiol
Chemical Properties
Molecular Weight460.73
FormulaC30H52O3
Cas No.7755-01-3
SmilesCC(C)=CCC[C@@](C)(O)[C@H]1CC[C@@]2(C)[C@@H]1[C@H](O)C[C@@H]1[C@@]3(C)CC[C@H](O)C(C)(C)[C@@H]3CC[C@@]21C
Relative Density.1.036 g/cm3 (Predicted)
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 10 mg/mL (21.7 mM), Sonication is recommended.
Chloroform, Dichloromethane, Ethyl Acetate, Acetone, etc.: Soluble
In Vivo Formulation
10% DMSO+90% Corn Oil: 1 mg/mL (2.17 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 mM2.1705 mL10.8523 mL21.7047 mL108.5234 mL
5 mM0.4341 mL2.1705 mL4.3409 mL21.7047 mL
10 mM0.2170 mL1.0852 mL2.1705 mL10.8523 mL
20 mM0.1085 mL0.5426 mL1.0852 mL5.4262 mL

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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:
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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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