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PROTACERα Degrader-6 (compound A3) is an effective PROTAC degrader of ERα with an IC50 of 0.12 μM in the MCE-7 cell line. It exhibits antitumor activity and serves as a fluorescent probe with an emission wavelength of 582 nm, enabling real-time visualization of ERα protein degradation.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | PROTACERα Degrader-6 (compound A3) is an effective PROTAC degrader of ERα with an IC50 of 0.12 μM in the MCE-7 cell line. It exhibits antitumor activity and serves as a fluorescent probe with an emission wavelength of 582 nm, enabling real-time visualization of ERα protein degradation. |
| Targets&IC50 | ERα:0.12 μM (DC50) |
| In vitro | PROTAC ERα Degrader-6 (compound A2) demonstrates significant anti-proliferative activity in MCF-7 cells with an IC50 of 0.11 μM. Additionally, PROTAC ERα Degrader-6 offers excellent fluorescence imaging capabilities at λ = 582 nm. |
| Formula | C51H56N6O8S |
| 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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