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AKT-IN-17 is an orally administered AKt inhibitor. It induces apoptosis (Apoptosis) by inhibiting AKt within A549 cells and is applicable to non-small cell lung cancer research.
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | AKT-IN-17 is an orally administered AKt inhibitor. It induces apoptosis (Apoptosis) by inhibiting AKt within A549 cells and is applicable to non-small cell lung cancer research. |
| Targets&IC50 | Akt2:105.88 μM |
| In vitro | AKT-IN-17 exhibits cytotoxic activity against A549 cells at a concentration of 176.32 μM, while it shows no effect on normal L929 cells, with an IC 50 of 176.32 μM. When applied at concentrations of 44.06, 88.12, and 176.23 μM for 24 hours, AKT-IN-17 inhibits AKt within A549 cells with an IC 50 of 105.88 μM. Additionally, at 176.23 μM for 24 hours, AKT-IN-17 induces early apoptosis in A549 cells by 3.26% and late apoptosis by 1.76%. |
| Formula | C21H21ClN4O2S |
| 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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