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STD1T is a selective and potent inhibitor of the deubiquitinase USP2a with potential anticancer activity that reduces cell cycle protein D1 protein levels in HCT116 colon and MCF-7 breast cancer cells.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $199 | - | In Stock |
| Description | STD1T is a selective and potent inhibitor of the deubiquitinase USP2a with potential anticancer activity that reduces cell cycle protein D1 protein levels in HCT116 colon and MCF-7 breast cancer cells. |
| In vitro | STD1T inhibits the enzymatic activity of USP2a in a concentration-dependent manner. It exhibits selective inhibition of USP2a compared to USP7 at concentrations of 10 µM and 2000 µM, respectively[1]. |
| Molecular Weight | 417.5 |
| Formula | C19H19N3O4S2 |
| Cas No. | 893075-58-6 |
| Smiles | NC(=O)c1c(NC(=O)COCc2cc(on2)-c2cccs2)sc2CCCCc12 |
| 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 | DMSO: 50 mg/mL (119.76 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
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DMSO
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