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Digoxin is a potent inhibitor of Na+/K+-ATPase, has the potential for arrhythmia and heart failure.
| Cell Experiment | |
|---|---|
| Cell lines | A549 cells |
| Preparation method | Cells were treated with various concentrations of digoxin for 24 h and seeded in transwell chambers (8-μm pore size, 6.5-mm diameter), which were or were not coated with Matrigel. The upper wells were filled with serum-free media and A549 cells (2×104 or 1×104 cells per well). The lower wells of the transwells contained the same media with 10% FBS and digoxin at various concentrations. |
| Concentrations | 250 nM |
| Incubation time | 24 h |
| Animal Experiment | |
|---|---|
| Animal models | Sprague Dawley Rats |
| Formulation | 0.5% sodium carboxymethylcellulose |
| Dosages | 25.6 μmol/kg |
| Administration | oral gavage |
| Molecular Weight | 780.94 |
| Formula | C41H64O14 |
| CAS Number | 20830-75-5 |
| Solubility (25°C) | DMSO 40 mg/mL |
| Storage | -20°C, protect from light, sealed |
| Related Sodium Channel Products |
|---|
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Rilutek is a sodium channel protein inhibitor and a new mental compound, which has anticonvulsant, hypnotic, antianxiety, antiischemia and anesthesia properties. Riluzole belongs to the family of use-dependent Na+ channel blocker which can also inhibit GABA uptake with an IC50 of 43 μM. |
| A-803467
A-803467 is a potent and selective Nav1.8 sodium channel blocker that potently blocks tetrodotoxin-resistant currents (IC50 = 140 nM). |
| Oxcarbazepine
Oxcarbazepine is an anticonvulsant and mood-stabilizing compound. |
| Ambroxol hydrochloride
AmbroxolHCl is a potent inhibitor of the neuronal Na+ channels, inhibits TTX-resistant Na+ currents with IC50 of 35.2 μM and 22.5 μM for tonic and phasic block, inhibits TTX-sensitive Na+ currents with IC50 of 100 μM. |
| Camostat mesylate
Camostat mesylate is a trypsin-like protease inhibitor, inhibits airway epithelial sodium channel (ENaC) function with IC50 of 50 nM, less potent to trpsin, prostasin and matriptase. |
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