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Ferroptosisinducer-11 is an agent that induces ferroptosis, exhibiting significant cytotoxicity against HCT-116, NCM-60, and HT-29 cells with IC50 values of 0.43 μM, 3.14 μM, and 0.48 μM, respectively. It potently inhibits GPX4 enzyme activity with an IC50 of 1.86 μM. This compound induces ferroptosis and increases lipid ROS, malondialdehyde (MDA), and Fe2+ levels in colon cancer cells while reducing glutathione (GSH) levels. Ferroptosisinducer-11 is useful for colon cancer research.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | Ferroptosisinducer-11 is an agent that induces ferroptosis, exhibiting significant cytotoxicity against HCT-116, NCM-60, and HT-29 cells with IC50 values of 0.43 μM, 3.14 μM, and 0.48 μM, respectively. It potently inhibits GPX4 enzyme activity with an IC50 of 1.86 μM. This compound induces ferroptosis and increases lipid ROS, malondialdehyde (MDA), and Fe2+ levels in colon cancer cells while reducing glutathione (GSH) levels. Ferroptosisinducer-11 is useful for colon cancer research. |
| Targets&IC50 | GPX4:1.86 μM |
| In vitro | Ferroptosis inducer-11 (Compound 30) demonstrates significant inhibitory activity on colony formation in HCT-116 colon cancer cells at concentrations of 0.25-1 μM over 24 hours. It exhibits potent cytotoxicity against HCT-116, NCM-60, and HT-29 cells, with IC 50 values of 0.43 μM, 3.14 μM, and 0.48 μM, respectively. In HCT-116 cells, Ferroptosis inducer-11 significantly increases lipid ROS levels in a time- and dose-dependent manner at 0.25-1 μM for 6-24 hours. It also elevates MDA levels, raises intracellular Fe 2+ levels, and decreases GSH levels in a dose-dependent manner at 0.25-1 μM over 12 hours. This compound strongly inhibits GPX4 with an IC 50 value of 1.86 μM and downregulates GPX4 protein expression in a time- and dose-dependent manner at 0.25-1 μM for 6-24 hours in HCT-116 cells. |
| 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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