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ST4206 is an antagonist of adenosine A2A. For adenosine A2A receptor and adenosine A1 receptor, the Kis values are 12 nM and 197 nM , respectively.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,820 | 8-10 weeks | 8-10 weeks | |
| 50 mg | $2,380 | 8-10 weeks | 8-10 weeks | |
| 100 mg | $3,100 | 8-10 weeks | 8-10 weeks |
| Description | ST4206 is an antagonist of adenosine A2A. For adenosine A2A receptor and adenosine A1 receptor, the Kis values are 12 nM and 197 nM , respectively. |
| Targets&IC50 | A1 receptor:197 nM(ki), A2A receptor:(ki)12 nM |
| In vitro | ST4206 inhibits agonist-induced cAMP accumulation with an IC50 of 990 nM [1]. |
| In vivo | ST4206, administered orally at doses of 10, 20, and 40 mg/kg, counteracts haloperidol-induced catalepsy and enhances motor activity in mice in a dose-dependent fashion. At dosages of 20 and 40 mg/kg, the compound markedly augments the number of contralateral turns in rats triggered by l-DOPA[1]. Demonstrating oral efficacy at concentrations of 10, 20, and 40 mg/kg, ST4206 effectively mitigates haloperidol-induced catalepsy in mice[2]. |
| Molecular Weight | 286.29 |
| Formula | C12H14N8O |
| Cas No. | 1246018-36-9 |
| Relative Density. | 1.61 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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