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160754-76-7

160754-76-7 Structure

160754-76-7 Structure
IdentificationBack Directory
[Name]

CNS-5161,N'-(2-CHLORO-5-METHYLSULFANYL-PHENYL)-N-METHYL-N-(3-METHYLSULFANYL-PHENYL)-GUANIDINE
[CAS]

160754-76-7
[Synonyms]

CNS5161
CNS 5161
N-(2-Chloro-5-methylthiophenyl)-N''-(3-methylthiophenyl)-N''-methylguanidine
Guanidine, N''-[2-chloro-5-(methylthio)phenyl]-N-methyl-N-[3-(methylthio)phenyl]-
CNS-5161,N'-(2-CHLORO-5-METHYLSULFANYL-PHENYL)-N-METHYL-N-(3-METHYLSULFANYL-PHENYL)-GUANIDINE
[Molecular Formula]

C16H18ClN3S2
[MDL Number]

MFCD09833785
[MOL File]

160754-76-7.mol
[Molecular Weight]

351.92
Chemical PropertiesBack Directory
[Appearance]

Yellowish oil
[Boiling point ]

465.4±55.0 °C(Predicted)
[density ]

1.25±0.1 g/cm3(Predicted)
[pka]

10.22±0.10(Predicted)
Hazard InformationBack Directory
[Chemical Properties]

Yellowish oil
[Uses]

CNS-5161 is a novel NMDA ion-channel antagonist that interacts with the NMDA receptor/ion channel site to produce a noncompetitive blockade of the actions of glutamate.
[in vivo]

In the neonatal rat NMDA excitotoxicity model in vivo, CNS-5161 (CNS 5161) protects against the necrotic effects of exogenous N-methyl-D-aspartate with an ED80 of 4 mg/kg by the intraperitoneal (i.p.) route. CNS-5161 also shows a 91% inhibition of audiogenic seizures in DBA/2 mice at 4 mg/kg i.p., and has a neuroprotective effect following hypoxix/ischaemic brain injury in neonatal rats[1].

[References]

[1] Walters MR, et al. Early clinical experience with the novel NMDA receptor antagonist CNS 5161. Br J Clin Pharmacol. 2002 Mar;53(3):305-11. DOI:10.1046/j.0306-5251.2001.01541.x
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