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PD-1/PD-L1 antagonist 1 (Compound A5) is an inhibitor of the interaction between programmed cell death protein 1 (PD-1) and programmed death-ligand 1 (PD-L1), with an IC50 value of 23.78 nM.
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | PD-1/PD-L1 antagonist 1 (Compound A5) is an inhibitor of the interaction between programmed cell death protein 1 (PD-1) and programmed death-ligand 1 (PD-L1), with an IC50 value of 23.78 nM. |
| In vitro | PD-1/PD-L1 antagonist 1 (0-3 μM) inhibits the interaction between PD-1 and PD-L1 in a dose-dependent manner within the Jurkat-NFAT-PD-1 and Hep3B-OS8-hPD-L1 cell co-culture systems. It does not exhibit significant cytotoxicity towards Jurkat cells at concentrations up to 3.3 μM. |
| Formula | C52H48Cl2N6O8 |
| 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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