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PZ703b TFA, a Bcl-xl PROTAC degradation agent, promotes apoptosis and halts bladder cancer cell proliferation, making it a pertinent investigative compound for related oncological studies [1] [2].
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| 5 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | PZ703b TFA, a Bcl-xl PROTAC degradation agent, promotes apoptosis and halts bladder cancer cell proliferation, making it a pertinent investigative compound for related oncological studies [1] [2]. |
| In vitro | PZ703b (0-1 μM, 24 h) TFA synergistically enhances the anti-proliferative effects of Mivebresib against bladder cancer cells in a dose-responsive manner while inducing apoptosis through the mitochondrial pathway [1]. PZ703b (0-1 μM, 48 h) TFA also potently inhibits MOLT-4 and RS4;11 cell lines, with IC50 values of 15.9 and 11.3 nM, respectively [2]. At 10 nM over 48 hours, PZ703b TFA induces significant and sustained BCL-XL degradation, leading to caspase-3 mediated apoptosis in MOLT-4 cells [2]. |
| Molecular Weight | 1714.46 |
| Formula | C82H103ClF6N10O13S4 |
| 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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