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ChemicalBook--->CAS DataBase List--->202402-01-5

202402-01-5

202402-01-5 Structure

202402-01-5 Structure
IdentificationBack Directory
[Name]

GET-73
[CAS]

202402-01-5
[Synonyms]

GET-73
GET 73;GET-73;GET73
[EINECS(EC#)]

805-308-6
[Molecular Formula]

C13H16F3NO2
[MOL File]

202402-01-5.mol
[Molecular Weight]

275.27
Chemical PropertiesBack Directory
[Boiling point ]

394.7±42.0 °C(Predicted)
[density ]

1.175±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO : 100 mg/mL (363.28 mM; Need ultrasonic)
[form ]

Solid
[pka]

15.11±0.46(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

GET73 is a γ-hydroxybutyric acid (GHB) analog, a naturally occurring neurotransmitter. GET73 has anti-alcohol and anxiolytic properties. GET73 significantly affects glutamate transmission in the hippocampus[1][2][3].
[in vivo]

GET73 (5-50 mg/kg; i.g.) exerts an anxiolytic effect in Sprague-Dawley rats exposed to the elevated plus maze (EPM) test[3].

Animal Model:Male SD rats (200-300?g and 300–350?g)[3]
Dosage:5 mg/kg, 10 mg/kg, 25 mg/kg, 50 mg/kg
Administration:Oral gavage
Result:Exerted an anxiolytic effect in rats exposed to the elevated plus maze (EPM) test.
[storage]

Store at -20°C
[References]

[1] Tomasini MC, et al. GET73 Prevents Ethanol-Induced Neurotoxicity in Primary Cultures of Rat Hippocampal Neurons. Alcohol Alcohol. 2016 Mar;51(2):128-35. DOI:10.1093/alcalc/agv094
[2] Ferraro L, et al. GET73 modulates rat hippocampal glutamate transmission: evidence for a functional interaction with mGluR5. Pharmacol Rep. 2011;63(6):1359-71. DOI:10.1016/s1734-1140(11)70700-9
[3] Loche A, et al. Anti-Alcohol and Anxiolytic Properties of a New Chemical Entity, GET73. Front Psychiatry. 2012 Feb 14;3:8. DOI:10.3389/fpsyt.2012.00008
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