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Apoptosis inducer46 is an apoptosis (apoptosis) inducer that exhibits potent and selective growth inhibitory effects on metastatic triple-negative breast cancer (TNBC) cells. It induces G2/M phase cell cycle arrest and apoptosis (apoptosis) cell death in MDA-MB-231 cells and blocks the nuclear translocation of NF-κB. Apoptosis inducer46 is useful for TNBC research.
| 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 | Apoptosis inducer46 is an apoptosis (apoptosis) inducer that exhibits potent and selective growth inhibitory effects on metastatic triple-negative breast cancer (TNBC) cells. It induces G2/M phase cell cycle arrest and apoptosis (apoptosis) cell death in MDA-MB-231 cells and blocks the nuclear translocation of NF-κB. Apoptosis inducer46 is useful for TNBC research. |
| In vitro | Apoptosis inducer 46 (Compound 5d) demonstrates potent growth inhibitory effects on metastatic triple-negative breast cancer (TNBC) cells, including MDA-MB-231, HCC 1806, MCF-7, and BEAS 2B cells, with IC 50 values of 0.38 μM, 0.31 μM, 0.39 μM, and 0.7 μM, respectively. Furthermore, at concentrations of 5-40 μM over 2-4 hours, it significantly reduces proteasome activity in MDA-MB-231 cells, with an IC 50 of 37.0 μM for proteasome inhibition, and leads to the accumulation of ubiquitinated proteins. At 5 μM across 24-72 hours, the compound elevates apoptosis rates and causes cell cycle arrest at the G2/M phase in MDA-MB-231 cells. Additionally, concentrations of 5-20 μM stabilize cyclin D1, p53, and p21 proteins, prevent the degradation of IκBα, IκBε, and IκKγ, and inhibit the nuclear translocation of NF-κB in MDA-MB-231 cells. |
| Molecular Weight | 375.47 |
| Formula | C24H25NO3 |
| Cas No. | 3085356-41-5 |
| Smiles | O=C1C(=CC2=CC=C(C=C2)C)CN(CC1=CC3=CC=C(O)C(OC)=C3)C4CC4 |
| 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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