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Nav1.8-IN-9 (Example 16), a potent Nav1.8 inhibitor with an IC 50 of 0.084 nM, is orally active and holds promise for extensive pain research [1].

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | Nav1.8-IN-9 (Example 16), a potent Nav1.8 inhibitor with an IC 50 of 0.084 nM, is orally active and holds promise for extensive pain research [1]. |
| Targets&IC50 | Nav1.8:0.084 nM |
| In vivo | Nav1.8-IN-9 (Example 16; 30 mg/kg; single oral dose) effectively inhibits mechanically-induced hypersensitivity in a rat postoperative pain model at 1, 2, and 4 hours [1]. |
| Molecular Weight | 496.48 |
| Formula | C22H20F4N4O3S |
| Cas No. | 2966089-14-3 |
| Smiles | C(NC1=CC(S(N)(=O)=O)=CC=C1)(=O)C=2C(=NC3=C(C2)C=C(F)C(F)=C3)N4CCC(F)(F)CCC4 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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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