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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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| 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). |
| Synonyms | Sodium polyoxotungstate hydrate, POM-1 hydrate |
| Molecular Weight | 3004.01 |
| Formula | H4Na6O41W12 |
| Cas No. | 314075-43-9 |
| Smiles | O=[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 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
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.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
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 ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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