| Name | N-(1-Phenylcyclohexyl)-1,5-pentanediamine dihydrobromide |
|---|
| Description | IEM-1925 bromide is an orally active glutamate receptor antagonist, increases the latent period and decreases the duration of status epilepticus in rats in a lithium-pilocarpine model of epilepsy[1][2]. |
|---|---|
| Related Catalog | |
| In Vivo | IEM-1925 (10 mg/kg) 减弱了大鼠癫痫状态下的行为运动惊厥症状,将Pinel和Rovner评分中的癫痫发作强度从8分降至4分。 Animal Model: Rats (males, weight 240-350 g)[2]. Dosage: 5, 10 mg/kg. Administration: i.m. Result: Administration of 5 and 10 mg/kg IEM-1925 2 h before pilocarpine did not alter the overall SE pattern. However, IEM-1925 significantly changed the latent periods of onset and durations of the separate phases and also decreased the total duration of status. |
| References |
| Molecular Formula | C17H30Br2N2 |
|---|---|
| Molecular Weight | 422.24 |
| Exact Mass | 420.07800 |
| PSA | 38.05000 |
| LogP | 6.57200 |