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Paeonoside

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Catalog No. TN6926Cas No. 20309-70-0

Paeonoside, found in P. suffruticosa, is biologically active and can promote wound healing and migration during osteoblast differentiation. Paeonoside has certain antidiabetic activity and may prevent sepsis and death from sepsis. Paeonoside has no cytotoxic effect on preosteoblasts of MC3T3-E1 cells, significantly restores the wound area and promotes cell migration and alkaline phosphatase (ALP) staining and its activity in a dose-dependent manner.

Paeonoside

Paeonoside

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Purity: 99.98%
Catalog No. TN6926Cas No. 20309-70-0
Paeonoside, found in P. suffruticosa, is biologically active and can promote wound healing and migration during osteoblast differentiation. Paeonoside has certain antidiabetic activity and may prevent sepsis and death from sepsis. Paeonoside has no cytotoxic effect on preosteoblasts of MC3T3-E1 cells, significantly restores the wound area and promotes cell migration and alkaline phosphatase (ALP) staining and its activity in a dose-dependent manner.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$117-In Stock
5 mg$293-In Stock
10 mg$429-In Stock
25 mg$653-In Stock
50 mg$888-In Stock
100 mg$1,180-In Stock
1 mL x 10 mM (in DMSO)$289-In 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:99.98%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
Paeonoside, found in P. suffruticosa, is biologically active and can promote wound healing and migration during osteoblast differentiation. Paeonoside has certain antidiabetic activity and may prevent sepsis and death from sepsis. Paeonoside has no cytotoxic effect on preosteoblasts of MC3T3-E1 cells, significantly restores the wound area and promotes cell migration and alkaline phosphatase (ALP) staining and its activity in a dose-dependent manner.
In vitro
Paeonoside (0.1-100 μM, 24 h) exhibited no cytotoxicity towards MC3T3-E1 pro-osteoblasts cells, even at concentrations ranging from 0.1 to 100 μM, when treated for 24 hours.[1]
When MC3T3-E1 preosteoblasts were induced to differentiate using osteogenic supplement (OS) medium, treatment with PASI (1-30 μM, 24 h) significantly enhanced wound area restoration and facilitated cell migration in a dose-dependent manner. Furthermore, PASI demonstrated a dose-dependent promotion of alkaline phosphatase (ALP) staining and activity.[1]
Chemical Properties
Molecular Weight328.31
FormulaC15H20O8
Cas No.20309-70-0
SmilesO(C1=C(C(C)=O)C=CC(OC)=C1)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O
Relative Density.1.414 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 22.5 mg/mL (68.53 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.0459 mL15.2295 mL30.4590 mL152.2951 mL
5 mM0.6092 mL3.0459 mL6.0918 mL30.4590 mL
10 mM0.3046 mL1.5230 mL3.0459 mL15.2295 mL
20 mM0.1523 mL0.7615 mL1.5230 mL7.6148 mL
50 mM0.0609 mL0.3046 mL0.6092 mL3.0459 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
%
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