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Stevioside

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🥰Excellent
Catalog No. T2911Cas No. 57817-89-7

A natural, noncaloric sweetener with a potency 300 times more than that of regular sucrose. Exhibits transepithelial p-aminohippurate transport via organic anion transport system interference.

Stevioside

Stevioside

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🥰Excellent
Purity: 99.89%
Catalog No. T2911Cas No. 57817-89-7
A natural, noncaloric sweetener with a potency 300 times more than that of regular sucrose. Exhibits transepithelial p-aminohippurate transport via organic anion transport system interference.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$35In StockIn Stock
50 mg$52In StockIn Stock
100 mg$77In StockIn Stock
500 mg$187In StockIn Stock
1 mL x 10 mM (in DMSO)$29In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.89%
Color:White to Yellow
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Product Introduction

Stevioside AI Summary
Stevioside exhibits multiple bioactivities, including inhibition of HIV1 reverse transcriptase (IC50 >200.0 µg/mL) and cytotoxicity against human Raji cells (cell viability 60.0%). The compound shows potent inhibition of TPA-induced EBV-early antigen activation in human Raji cells, with activities ranging from 100.0% at a 10 molar ratio to 12.5% at a 1000 molar ratio. It also demonstrates antioxidant activity with a hydroxyl radical scavenging IC50 value of 1500000.0 nM, and agonist activity at the glucocorticoid receptor in mouse RAW264.7 cells, with a firefly/renilla luciferase ratio of 1.96 at 10 µM concentration. In sensory evaluations, Stevioside displays sweet taste properties at 500 p.p.m., with a sweetness intensity relative to 10% sucrose (Ip = 0.9), high potency by weight (Pw = 190.0), and molar basis (Pm = 440.0). The sensory scores are 62.0 for sweetness, 30.0 for bitterness, and 8.0 for other properties. In animal models, Stevioside shows varied bioactivities related to renal excretion in Wistar rats, influencing renal clearance and excretion mechanisms depending on dosage. It also induces insulin sensitivity in Syrian golden hamsters, increasing glucose uptake 2.1-fold under normal conditions and 4.4-fold under insulin-resistant conditions, while downregulating glucose uptake in the jejunum by 43.0% at 1 mM after 60 minutes. Additionally, the compound inhibits DMBA-induced/TPA-promoted and peroxynitrite-induced/TPA-promoted carcinogenesis in Sencar mice, reducing the number of skin papillomas per mouse and showing reductions after a 20-week treatment duration. In terms of toxicity, Stevioside displays acute toxicity in mice with LD50 values greater than 15000.0 mg/kg and 8200.0 mg/kg for different assessments..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
A natural, noncaloric sweetener with a potency 300 times more than that of regular sucrose. Exhibits transepithelial p-aminohippurate transport via organic anion transport system interference.
Chemical Properties
Molecular Weight804.87
FormulaC38H60O18
Cas No.57817-89-7
SmilesC[C@@]12CCC[C@](C)(C1CC[C@@]13CC(=C)[C@](C1)(CCC23)O[C@H]1O[C@H](CO)C(O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(=O)O[C@@H]1O[C@H](CO)C(O)[C@H](O)C1O
Relative Density.1.53 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80.5 mg/mL (100.02 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 3.3 mg/mL (4.1 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 mM1.2424 mL6.2122 mL12.4244 mL62.1218 mL
5 mM0.2485 mL1.2424 mL2.4849 mL12.4244 mL
10 mM0.1242 mL0.6212 mL1.2424 mL6.2122 mL
20 mM0.0621 mL0.3106 mL0.6212 mL3.1061 mL
50 mM0.0248 mL0.1242 mL0.2485 mL1.2424 mL
100 mM0.0124 mL0.0621 mL0.1242 mL0.6212 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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

Tech Support

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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