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WSD0628 is a brain-penetrant and potent ATM inhibitor with a significant radiosensitizing effect [1].

| 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 | WSD0628 is a brain-penetrant and potent ATM inhibitor with a significant radiosensitizing effect [1]. |
| In vitro | WSD0628 significantly enhanced the radiosensitivity of U251 cells in clonogenic survival assays (0 nM vs. 30 nM at 5 Gy, p<0.01) [1]. |
| In vivo | WSD0628 (10 mg/kg, combined with a single 12.5 Gy dose) significantly enhances treatment efficacy in the melanoma brain metastasis M12 PDX model [1]. |
| Molecular Weight | 439.46 |
| Formula | C23H23F2N5O2 |
| Cas No. | 2765448-96-0 |
| Smiles | O=C1N(C=2C=3C(N=CC2N1C)=CC=C(C3)C=4C=CC(OC)=NC4)[C@H]5C(F)(F)CN(C)CC5 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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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