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Sodium metatungstate hydrate

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Catalog No. T208708Cas No. 314075-43-9
Alias Sodium polyoxotungstate hydrate, POM-1 hydrate

Sodium metatungstate (Sodium polyoxotungstate; POM-1) hydrate is an inhibitor of NTPDase, with Ki values for NTPDase1 (CD39), NTPDase 3, and NTPDase 2 being 2.58 μM, 3.26 μM, and 28.8 μM, respectively. It exhibits anti-inflammatory and anticancer properties and inhibits ATP hydrolysis while also blocking central synaptic transmission.

Sodium metatungstate hydrate

Sodium metatungstate hydrate

😃Good
Catalog No. T208708Alias Sodium polyoxotungstate hydrate, POM-1 hydrateCas No. 314075-43-9
Sodium metatungstate (Sodium polyoxotungstate; POM-1) hydrate is an inhibitor of NTPDase, with Ki values for NTPDase1 (CD39), NTPDase 3, and NTPDase 2 being 2.58 μM, 3.26 μM, and 28.8 μM, respectively. It exhibits anti-inflammatory and anticancer properties and inhibits ATP hydrolysis while also blocking central synaptic transmission.
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Product Introduction

Bioactivity
Description
Sodium metatungstate (Sodium polyoxotungstate; POM-1) hydrate is an inhibitor of NTPDase, with Ki values for NTPDase1 (CD39), NTPDase 3, and NTPDase 2 being 2.58 μM, 3.26 μM, and 28.8 μM, respectively. It exhibits anti-inflammatory and anticancer properties and inhibits ATP hydrolysis while also blocking central synaptic transmission.
In vitro
Sodium metatungstate hydrate (100 μM, 15 min) inhibits ATP-induced anionic dye uptake and large pore formation in macrophages. Additionally, Sodium metatungstate hydrate (100 μM, 8 h) suppresses ATP-induced P2X7-related pyroptosis in macrophages. Furthermore, Sodium metatungstate hydrate (100 μM, 8-24 h) exhibits significant anti-inflammatory effects on macrophages.
In vivo
Sodium metatungstate hydrate (5 mg/kg, intraperitoneal injection, single dose) exhibits distinct cytokine/chemokine responses in the peritoneum and systemic circulation of CD39 knockout mice. Furthermore, when combined with anti-CD73 antibody and AZD4635, sodium metatungstate hydrate (5 mg/kg, intraperitoneal injection, once daily, from day 0 to day 4, day 7 to day 11, and day 14 to day 18) effectively reduces tumor burden in mice with multiple myeloma (MM).
SynonymsSodium polyoxotungstate hydrate, POM-1 hydrate
Chemical Properties
Molecular Weight3004.01
FormulaH4Na6O41W12
Cas No.314075-43-9
SmilesO=[W+4]1234[O-2][W+4]567([O-2][W+4]89%10([O-2][W+4]%11%12([O-2]1)([O-2][W+4]%13([O-2]8)([O-2][W+4]%14%15%16([O-2][W+4]%17([O-2]2)([O-2]%11)([O-2][W+4]%18([O-2][W+4]([O-2]3)([O-2]5)([O-2][W+4]%19%20([O-2][W+4]%21([O-2]6)([O-2]9)([O-2][W+4]([O-2]%13)([O-2]%14)([O-2]%19)([OH-]%21%20)=O)=O)([O-2]%18)=O)([O-2]47)=O)([O-2]%15)([OH-]%17%16)=O)=O)=O)([O-2]%12%10)=O)=O)=O)=O.[Na+].O.[Na+].[Na+].[Na+].[Na+].[Na+]
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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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:
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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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