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Carisbamate (RWJ-333369) is an orally active neuromodulator that suppresses the development and propagation of epileptiform discharges, confers neuroprotection following epilepticus-like injury in vitro, and demonstrates robust antiepileptic efficacy in genetic models of generalized and nonconvulsive epilepsy, supporting its translational relevance in epilepsy research.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $30 | - | In Stock | |
| 5 mg | $68 | - | In Stock | |
| 10 mg | $112 | - | In Stock | |
| 25 mg | $226 | - | In Stock | |
| 50 mg | $339 | - | In Stock | |
| 100 mg | $513 | - | In Stock |
| Description | Carisbamate (RWJ-333369) is an orally active neuromodulator that suppresses the development and propagation of epileptiform discharges, confers neuroprotection following epilepticus-like injury in vitro, and demonstrates robust antiepileptic efficacy in genetic models of generalized and nonconvulsive epilepsy, supporting its translational relevance in epilepsy research. |
| In vitro | In cultured hippocampal neurons, Carisbamate (200 μM) acutely inhibited spontaneous recurrent epileptiform discharges (SREDs) after 12 hours in over 95% of neurons, with effects maintained for 24 hours [1]. |
| In vivo | In the Genetic Absence Epilepsy Rat from Strasbourg (GAERS) model, intraperitoneal (i.p.) administration of Carisbamate (10, 30, 60 mg/kg) reduced the expression of spike-and-wave discharges (SWD) dose-dependently. The 60 mg/kg dose completely inhibited SWD after 120 minutes. In audiogenic sensitive Wistar AS rats, Carisbamate (20, 30 mg/kg, i.p.) prevented wild running episodes and tonic seizures in all animals. At 10 mg/kg, the latency to tonic seizure was increased by 327% [6]. |
| Synonyms | RWJ-333369, RWJ333369, RWJ 333369, JNJ-10234094, JNJ10234094 |
| Molecular Weight | 215.63 |
| Formula | C9H10ClNO3 |
| Cas No. | 194085-75-1 |
| Smiles | [C@H](COC(N)=O)(O)C1=C(Cl)C=CC=C1 |
| Relative Density. | no data available |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (371.01 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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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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