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PROTACPD-L1 degrader-1 is a CRBN-based PD-L1-PROTAC degrader with significant PD-L1 protein degradation capacity. It demonstrates strong PD-L1 degradation activity in 4T1 cells, with a DC50 of 0.609 μM. This compound is applicable to breast cancer research.
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | PROTACPD-L1 degrader-1 is a CRBN-based PD-L1-PROTAC degrader with significant PD-L1 protein degradation capacity. It demonstrates strong PD-L1 degradation activity in 4T1 cells, with a DC50 of 0.609 μM. This compound is applicable to breast cancer research. |
| Targets&IC50 | Cereblon:131.77 μM (kd) |
| In vitro | PROTAC PD-L1 degrader-1 (compound PA8; 0.078-10 μM; 24 hours) significantly degrades PD-L1 protein in 4T1 cells in a dose-dependent manner. It exhibits specific binding to CRBN and PD-L1 with dissociation constant (K d) values of 131.77 μM and 59.2 μM, respectively, both showing concentration dependency. |
| In vivo | PROTAC PD-L1 degrader-18 (30-60 mg/kg; intraperitoneal injection; once daily for 15 days) effectively reduces both tumor volume and weight in a 4T1 tumor-bearing mouse model. |
| 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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