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PLK1/BRD4-IN-5 (Compound SC10) is an orally active inhibitor of PLK1 and BRD4, exhibiting IC50 values of 0.3 nM and 60.8 nM, respectively. It induces S phase cell cycle arrest and dose-dependent apoptosis in MV4-11 cells. PLK1/BRD4-IN-5 is useful for cancer research.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | PLK1/BRD4-IN-5 (Compound SC10) is an orally active inhibitor of PLK1 and BRD4, exhibiting IC50 values of 0.3 nM and 60.8 nM, respectively. It induces S phase cell cycle arrest and dose-dependent apoptosis in MV4-11 cells. PLK1/BRD4-IN-5 is useful for cancer research. |
| Targets&IC50 | PLK1:0.3 nM, BRD4:60.8 nM |
| In vitro | PLK1/BRD4-IN-5 (Compound SC10) exhibits significant antiproliferative activity against three tumor cell lines with IC50 values of 17.3 nM for MDA-MB-231, 8.4 nM for MDA-MB-361, and 5.4 nM for MV4-11. |
| Formula | C31H44N8O3 |
| 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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