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Synonyms:
Nav1.5-IN-1
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | Nav1.5-IN-1 is a selective Nav1.5 inhibitor with an IC50 of 1.38 μM, demonstrating specificity towards other Nav subtypes. It reduces the cardiac conduction velocity in isolated rat hearts and is applicable in arrhythmia research. |
| Targets & IC50 | Nav1.5:1.38 μM |
| In vitro | Nav1.5-IN-1 (KH2) is a potent inhibitor of the wild-type human Nav1.5 in HEK293T cells, with an IC50 of 1.38 μM, and shows selectivity for other Nav subtypes. In MD simulations, Nav1.5-IN-1 (KH2) (500 ns) stably binds to the central cavity pocket of human Nav1.5, primarily interacting with residues C896, L931, and F1760. The compound mildly inhibits hERG currents in HEK293T cells with an IC50 of 10.32 μM and does not significantly inhibit Kir2.1 at a concentration of 20 μM. |
| In vivo | Administered as a single dose of 35 mg/kg via intraperitoneal injection, Nav1.5-IN-1 (KH2) does not induce acute systemic or neurobehavioral toxicity in 8-week-old mice. |
| Molecular Weight | 642.21 |
| Formula | C36H36ClN3O4S |
| Cas No. | 899207-91-1 |
| Smiles | O=C(NCCCN1CCC(CC=2C=CC=CC2)CC1)C3=CC=C4C(=C3)N(C(=O)C=5C=CC=CC5S4(=O)=O)CC=6C=CC=C(Cl)C6 |
| 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.
| Size | Quantity | Unit Price | Amount | Operation |
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