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PD-1/PD-L1-IN-41 (Compound 5c) is an inhibitor of PD-L1 and PD-1 with an IC50 value of 10.2 nM.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | PD-1/PD-L1-IN-41 (Compound 5c) is an inhibitor of PD-L1 and PD-1 with an IC50 value of 10.2 nM. |
| In vitro | PD-1/PD-L1-IN-41 (Compound 5c) exhibits an EC50 of 11.6 μM against CHO-hPD-L1 cells when administered at 100 μl for 24 hours. |
| In vivo | PD-1/PD-L1-IN-41 (Compound 5c) can be labeled with carbon-11 for radioactivity. In NSG mice, both PD-1-negative and PD-1-expressing xenografts exhibit no specific binding to [11C]5c. This lack of specificity could be due to the rapid metabolism of the radiotracer, limited tissue penetration from plasma protein binding, or increased levels of nonspecific or off-target interactions. |
| Formula | C33H32ClN3O5 |
| 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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