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Scr-IN-2 is an effective c-Scr inhibitor with an IC50 of 302 nM, demonstrating nanomolar-level activity against breast cancer. It elevates cellular ROS levels, induces mitochondrial damage, causes G1 phase arrest, and triggers apoptosis (apoptosis). Scr-IN-2 is applicable for research in breast cancer studies.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | Scr-IN-2 is an effective c-Scr inhibitor with an IC50 of 302 nM, demonstrating nanomolar-level activity against breast cancer. It elevates cellular ROS levels, induces mitochondrial damage, causes G1 phase arrest, and triggers apoptosis (apoptosis). Scr-IN-2 is applicable for research in breast cancer studies. |
| In vitro | Scr-IN-2 (Compound 3g) effectively inhibits the proliferation of MDAMB-231, T47D, and MCF-7 cells with IC50 values of 0.812, 1.03, and 0.568 μM, respectively, while showing no significant toxicity to normal breast cells (MCF-10A). Scr-IN-20 (500 nM, 48 h) increases reactive oxygen species (ROS) production, causes mitochondrial damage, induces apoptosis, and arrests the cell cycle of MCF-7 cells in the G1 phase. |
| Molecular Weight | 383.54 |
| Formula | C21H33N7 |
| Cas No. | 2787582-78-7 |
| Smiles | N=1N=C(N(N1)C(C)(C)C)C2C=3C=CC=CC3N=C(NC(C)(C)C)N2CCCC |
| 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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