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BW A868C, a hydantoin compound and structural analogue of BW245C, functions as a selective and potent competitive antagonist of prostaglandin D2 (PGD2), showing no activity on other prostaglandin receptors (IP, EP1, EP2, TP, and FP) [1].

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $218 | 35 days | 35 days | |
| 5 mg | $960 | 35 days | 35 days | |
| 10 mg | $1,700 | 35 days | 35 days |
| Description | BW A868C, a hydantoin compound and structural analogue of BW245C, functions as a selective and potent competitive antagonist of prostaglandin D2 (PGD2), showing no activity on other prostaglandin receptors (IP, EP1, EP2, TP, and FP) [1]. |
| In vitro | BW A868C antagonizes PGD2- and BW245C-induced activation of human platelet adenylate cyclase [1]. |
| Molecular Weight | 459.58 |
| Formula | C25H37N3O5 |
| Cas No. | 118675-50-6 |
| Smiles | N(CC(O)C1CCCCC1)N2C(CCCCCCC(O)=O)C(=O)N(CC3=CC=CC=C3)C2=O |
| Relative Density. | 1.24 g/cm3 (Predicted) |
| 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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