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ARB-272572 is a potent inhibitor of programmed cell death ligand 1 (PD-L1) signaling that induces PD-L1 homodimer interactions and produces immunostimulatory activity in human primary cells.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $132 | In Stock | In Stock | |
| 5 mg | $328 | In Stock | In Stock | |
| 10 mg | $473 | In Stock | In Stock | |
| 25 mg | $792 | In Stock | In Stock | |
| 50 mg | $1,150 | In Stock | In Stock | |
| 100 mg | $1,650 | - | In Stock | |
| 200 mg | $2,220 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $392 | In Stock | In Stock |
| Description | ARB-272572 is a potent inhibitor of programmed cell death ligand 1 (PD-L1) signaling that induces PD-L1 homodimer interactions and produces immunostimulatory activity in human primary cells. |
| Targets&IC50 | PD-1/PD-L1:400 pM |
| In vitro | METHODS: Small molecules were screened in a cell-free in vitro homogeneous time-resolved fluorescence (HTRF) assay using αPD-L1 (MIH1) and αPD-1 (nivolumab) antibodies as positive controls.
RESULTS: ARB-272572 inhibited PD-1/PD-L1 with an IC50 value of 400 pM.[1] |
| In vivo | "METHODS: PD-1/PD-L1 humanized mice implanted with MC38 cells expressing humanized PD-L1 and treated with ARB-272572 (10 mg/kg orally, 7 times daily, days 0-6) or αPD-L1 (10 mg/kg intraperitoneally, 3 times per week, days 0-16). Statistically significant tumor growth inhibition was observed with αPD-L1 antibody or Compound A treatment.
RESULTS:ARB-272572 treatment resulted in a 60.4% reduction in mean tumor volume in 60.4% of mice after only 7 days. [1]" |
| Synonyms | ARB272572, ARB 272572 |
| Molecular Weight | 568.67 |
| Formula | C32H36N6O4 |
| Cas No. | 2368182-63-0 |
| Smiles | O=C(NC1=CC=CC(C=2C=CC=C(NC(=O)C3=NC=C(C=C3)CNCCO)C2C)=C1C)C4=NC=C(C=C4)CNCCO |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 150 mg/mL (263.77 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween-80+45% Saline: 3.3 mg/mL (5.8 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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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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