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L791943 is a selective, potent) inhibitor of Phosphodiesterase-4 (PDE4,IC50 of 4.2 nM).

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,970 | 8-10 weeks | 8-10 weeks | |
| 50 mg | $2,580 | 8-10 weeks | 8-10 weeks | |
| 100 mg | $3,400 | 8-10 weeks | 8-10 weeks |
| Description | L791943 is a selective, potent) inhibitor of Phosphodiesterase-4 (PDE4,IC50 of 4.2 nM). |
| Targets&IC50 | PDE4:4.2 nM |
| In vitro | The metabolic stability of L791943 was assessed in vitro using rat hepatocytes and compared to that of CDP-840. Our results, under standard incubation conditions, show that more than 98% of L791943 remains unmetabolized, whereas only 11% of CDP-840 retains its original form. |
| Molecular Weight | 573.38 |
| Formula | C24H17F10NO4 |
| Cas No. | 192767-01-4 |
| Smiles | C(CC=1C=CN(=O)=CC1)(C2=CC(OC(F)F)=C(OC(F)F)C=C2)C3=CC=C(C(C(F)(F)F)(C(F)(F)F)O)C=C3 |
| Relative Density. | 1.44 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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