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ChemicalBook--->CAS DataBase List--->153322-06-6

153322-06-6

153322-06-6 Structure

153322-06-6 Structure
IdentificationBack Directory
[Name]

Lanicemine dihydrochloride
[CAS]

153322-06-6
[Synonyms]

AZD6765
ARL-15896
Lanicemine 2HCl
AZD6765 dihydrochloride
Lanicemine hydrochloride
FPL 15896 dihydrochloride
Lanicemine dihydrochloride
AR-R 15896 dihydrochloride
AZD6765 dihydrochloride >=97% (HPLC)
(αS)-α-Phenyl-2-pyridineethanamine dihydrochloride
ARL15896; ARL 15896; LANICEMINE HYDROCHLORIDE; AR-R15896AR
[Molecular Formula]

C13H16Cl2N2
[MOL File]

153322-06-6.mol
[Molecular Weight]

234.73
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

H2O: soluble20mg/mL, clear
[form ]

powder
[color ]

white to beige
[optical activity]

[α]/D +77 to +90°, c =1 in methanol
[Water Solubility ]

H2O: 20mg/mL, clear
Safety DataBack Directory
[Symbol(GHS) ]


GHS06
[Signal word ]

Danger
[Hazard statements ]

H301
[Precautionary statements ]

P301+P310
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

AZD6765 dihydrochloride has been used as an antidepressant?to improve behavior and metabolic measures?in chronic unpredictable mild stress (CUMS).
[Biochem/physiol Actions]

AZD6765 is a noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist and fast-acting antidepressant. In a recent study AZD6765 relieved depression within 80 minutes, unlike most antidepressants acting on serotonin or dopamine systems which can take several weeks to work. The effects lasted from about an hour up to 2 weeks. AZD6765 has an IC50 value of 1.3 μM. Unlike more potent drugs such as ketamine, which also has rapid antidepressant activity, AZD6765 has no dissociative side-effects such as hallucinations. Earlier studies inidcated the compound has neuroprotective and anticonvulsant effects.
[in vivo]

Lanicemine produces sustained antidepressant efficacy with minimal psychotomimetic adverse effects[1]. Lanicemine (3, 10 or 30 mg/kg; intraperitoneal) not only engages brain circuits involved in the generation of gamma- electroencephalography (EEG), but also influences these networks independent of the broader systems-level disruptions typical of ketamine[1].

Animal Model:Male Sprague-Dawley rats[1]
Dosage:3, 10 or 30?mg/kg
Administration:Intraperitoneal
Result:Produced pronounced dose-dependent elevations in spontaneous gamma-band EEG, but only gamma changes for Ketamine were tightly coupled to increases in locomotor activity.
[IC 50]

NMDA Receptor
[storage]

Store at -20°C
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