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Uridine 5′-diphosphoglucose disodium salt

(Synonyms: Uridine 5'-diphosphoglucose disodium sal, UDP-α-D-Glucose sodium salt, UDP-Glucose sodium salt, UDPG sodium salt) Copy Product Info
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Synonyms: Uridine 5'-diphosphoglucose disodium sal, UDP-α-D-Glucose sodium salt, UDP-Glucose sodium salt, UDPG sodium salt

Catalog No. T4743 Copy Product Info
Purity: 99.83%
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Uridine 5′-diphosphoglucose disodium salt (UDP-glucose) is a natural product and a P2Y14 receptor agonist (EC50 = 0.35 μM) with endogenous activity and selectivity. It is used for studying mechanisms related to cardiac inflammation following myocardial infarction/reperfusion injury.
Uridine 5′-diphosphoglucose disodium salt
Cas No. 28053-08-9
Pack SizePriceUSA StockGlobal StockQuantity
100 mg$42In StockIn Stock
500 mg$95In StockIn Stock
For In stock only · 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:99.83%
Color:White
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Product Introduction

Bioactivity
Description
Uridine 5′-diphosphoglucose disodium salt (UDP-glucose) is a natural product and a P2Y14 receptor agonist (EC50 = 0.35 μM) with endogenous activity and selectivity. It is used for studying mechanisms related to cardiac inflammation following myocardial infarction/reperfusion injury.
Targets & IC50
P2Y14 receptor:0.35 μM (EC50)
In vitro
Methods: Neutrophils were treated with Uridine 5′-diphosphoglucose disodium salt (0-100 μM) for 24 hours. P2Y14 receptor expression and cell apoptosis were detected.
Results: Uridine 5′-diphosphoglucose disodium salt upregulated P2Y14 receptor expression and induced neutrophil apoptosis. [1]
Methods: Mouse neutrophils were incubated with PPTN alone or combined with UDP-Glu (1 μM) for 24 hours. Cell viability was detected by CCK-8 assay, apoptosis and polarization (N1/N2) were detected by flow cytometry, migration ability was detected by Transwell, and P2Y14 expression was detected by Western Blot.
Results: PPTN significantly reversed UDP-Glu-induced decreased cell viability, increased apoptosis, and inhibited migration, promoted N2 polarization, and reduced inflammatory factor expression. [2]
SynonymsUridine 5'-diphosphoglucose disodium sal, UDP-α-D-Glucose sodium salt, UDP-Glucose sodium salt, UDPG sodium salt
Chemical Properties
Molecular Weight610.27
FormulaC15H22N2Na2O17P2
Cas No.28053-08-9
Smiles[Na+].[Na+].OC[C@@H](OP(=O)(OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1ccc(=O)[nH]c1=O)OP([O-])([O-])=O)[C@@H](O)[C@H](O)[C@@H](O)C=O
Relative Density.no data available
Storage & Solubility Information
StorageStore under nitrogen,Keep away from moisture Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 125 mg/mL (204.83 mM), Sonication is recommended.
DMSO: 128.75 mg/mL (210.97 mM)
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (8.19 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
H2O/DMSO
1mg5mg10mg50mg
1 mM1.6386 mL8.1931 mL16.3862 mL81.9309 mL
5 mM0.3277 mL1.6386 mL3.2772 mL16.3862 mL
10 mM0.1639 mL0.8193 mL1.6386 mL8.1931 mL
20 mM0.0819 mL0.4097 mL0.8193 mL4.0965 mL
50 mM0.0328 mL0.1639 mL0.3277 mL1.6386 mL
100 mM0.0164 mL0.0819 mL0.1639 mL0.8193 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
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

Keywords

Related Tags: Uridine 5′-diphosphoglucose disodium salt chemical structure | Uridine 5′-diphosphoglucose disodium salt in vitro | Uridine 5′-diphosphoglucose disodium salt formula | Uridine 5′-diphosphoglucose disodium salt molecular weight