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S 1924 is an effective inhibitor of H+, K+-ATPase, exhibiting IC50 values of 10.3 μM at pH 7.4 and 1.6 μM at pH 6.0.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | S 1924 is an effective inhibitor of H+, K+-ATPase, exhibiting IC50 values of 10.3 μM at pH 7.4 and 1.6 μM at pH 6.0. |
| In vitro | S 1924 inhibits histamine and dbc-AMP stimulated 14 C-aminopyrine uptake. |
| In vivo | S 1924, administered intravenously at a dose of 0.5 mg/kg, effectively inhibits gastric acid secretion in rats with gastric luminal perfusion stimulated by (gastrin-releasing peptide) (100 μg/kg/h, intravenous injection). |
| Molecular Weight | 277.37 |
| Formula | C12H11N3OS2 |
| Cas No. | 111371-30-3 |
| Smiles | O=S(C1=NC2=CSC=C2N1)CC3=NC=C(C=C3)C |
| 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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