IEM 1925 dihydrobromide

Modify Date: 2024-01-15 20:50:36

IEM 1925 dihydrobromide Structure
IEM 1925 dihydrobromide structure
Common Name IEM 1925 dihydrobromide
CAS Number 258282-23-4 Molecular Weight 422.24
Density N/A Boiling Point N/A
Molecular Formula C17H30Br2N2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of IEM 1925 dihydrobromide


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].

 Names

Name N-(1-Phenylcyclohexyl)-1,5-pentanediamine dihydrobromide

 IEM 1925 dihydrobromide Biological Activity

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

[1]. D B Tikhonov, et al. Voltage-dependent block of native AMPA receptor channels by dicationic compounds. Br J Pharmacol. 2000 Jan;129(2):265-74.  

[2]. S. I. Vataev, et al. IEM-1925, a Glutamate Receptor Channel Blocker, Increases the Latent Period and Decreases the Duration of Status Epilepticus in Rats in a Lithium-Pilocarpine Model of Epilepsy. Neuroscience and Behavioral Physiology volume 51, pages976–984 (2021).

 Chemical & Physical Properties

Molecular Formula C17H30Br2N2
Molecular Weight 422.24
Exact Mass 420.07800
PSA 38.05000
LogP 6.57200
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