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ATP-γ-S tetrasodium (Adenosine-5'-O-(3-thiotriphosphate) tetrasodium) is a purinergic P2Y11 receptor agonist and ATP analog that induces inositol phosphate accumulation, induces insulin secretion from MIN6 pancreatic islet β-cells, and induces an increase in intracellular calcium concentration. ATP-γ-S tetrasodium inhibits the induction of the Junin virus. Junin virus-induced increase in the level of mRNA encoding bone morphogenetic protein 6 (BMP6) reduces particle-forming units (PFUs) in Junin virus-infected primary rat osteoblasts.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 2600 μg | $398 | 35 days | 35 days |
| Description | ATP-γ-S tetrasodium (Adenosine-5'-O-(3-thiotriphosphate) tetrasodium) is a purinergic P2Y11 receptor agonist and ATP analog that induces inositol phosphate accumulation, induces insulin secretion from MIN6 pancreatic islet β-cells, and induces an increase in intracellular calcium concentration. ATP-γ-S tetrasodium inhibits the induction of the Junin virus. Junin virus-induced increase in the level of mRNA encoding bone morphogenetic protein 6 (BMP6) reduces particle-forming units (PFUs) in Junin virus-infected primary rat osteoblasts. |
| In vitro | ATP-γ-S tetrasodium enhances spinach Rubisco activase activity by enhancing autofluorescence and inducing aggregation. [1] ATP-γ-S tetrasodium (final blood concentration 50-100 μM) attenuated the inflammatory response as evidenced by a 48% reduction in cell accumulation and a 57% reduction in protein content in bronchoalveolar lavage fluid, as well as a reduction in neutrophil infiltration and a decrease in the number of neutrophils. exudation of Evans blue albumin dye in lung tissue. [3] |
| In vivo | 50 μM ATP-γ-S tetrasodium, i.v., protected lung parenchymal structures. [3] In LPS-treated mice, ATP-γ-S tetrasodium showed a dose-dependent effect on EBA exudation. [3] |
| Synonyms | ATPγS tetrasodium, Adenosine-5'-O-(3-thiotriphosphate) tetrasodium, Adenosine 5'-(γ-thio)-triphosphate tetrasodium |
| Molecular Weight | 611.17 |
| Formula | C10H12N5Na4O12P3S |
| Cas No. | 88453-52-5 |
| Smiles | O[C@H]1[C@@H](O[C@@H]([C@H]1O)COP(OP(OP([O-])([S-])=O)([O-])=O)([O-])=O)N2C3=NC=NC(N)=C3N=C2.[Na+].[Na+].[Na+].[Na+] |
| Storage | store 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 | H2O: 5 mg/mL (8.18 mM), Sonication is recommended. | |||||||||||||||
Solution Preparation Table | ||||||||||||||||
H2O
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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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