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MS15 TFA is a potent, selective AKT PROTAC degrader, effectively inhibiting AKT1, AKT2, and AKT3 with IC50 values of 798 nM, 90 nM, and 544 nM, respectively [1].
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| 5 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | MS15 TFA is a potent, selective AKT PROTAC degrader, effectively inhibiting AKT1, AKT2, and AKT3 with IC50 values of 798 nM, 90 nM, and 544 nM, respectively [1]. |
| In vitro | MS15 (0-10 μM, 24 hours) TFA effectively induces AKT degradation in SW620 cells and MS21 resistant cells harboring KRAS/BRAF mutations [1]. Furthermore, MS15 (0-10 μM, 5 days) TFA suppresses the proliferation of KRAS mutant SW620 cells [1]. In a time- and UPS-dependent manner, MS15 (1 μM, 1-24 hours) TFA mediates AKT degradation [1]. |
| In vivo | MS15, administered intraperitoneally at a dose of 75 mg/kg in a single injection, exhibits bioavailability [1] in mice. |
| Molecular Weight | 1228.47 |
| Formula | C66H80F3N11O7S |
| 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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