ChemicalBook--->CAS DataBase List--->39069-52-8

39069-52-8

39069-52-8 Structure

39069-52-8 Structure
IdentificationBack Directory
[Name]

GS 39783
[CAS]

39069-52-8
[Synonyms]

GS 39783
N,N'-DICYCLOPENTYL-2-(METHYLTHIO)-5-NITRO-4,6-PYRIMIDINEDIAMINE
N,N'-Dicyclopentyl-2-(methylthio)-5-nitro-4,6-pyrimidinediaamine
N4,N6-Dicyclopentyl-2-(methylthio)-5-nitropyrimidine-4,6-diamine
4,6-Pyrimidinediamine, N4,N6-dicyclopentyl-2-(methylthio)-5-nitro-
N,N'-DICYCLOPENTYL-2-METHYLSULFANYL-5-NITRO-PYRIMIDINE-4,6-DIAMINE
[Molecular Formula]

C15H23N5O2S
[MDL Number]

MFCD06201849
[MOL File]

39069-52-8.mol
[Molecular Weight]

337.44
Chemical PropertiesBack Directory
[storage temp. ]

Store at RT
[solubility ]

DMSO: ~8 mg/mL
[form ]

powder
[color ]

yellow
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

GS 39783 is an allosteric positive modulator of GABAB receptors. GS 39783 attenuates acute cocaine-induced hyperlocomotion and blocks cocaine-induced Fos induction in the striatal complex.
[Definition]

ChEBI: N4,N6-dicyclopentyl-2-(methylthio)-5-nitropyrimidine-4,6-diamine is an aryl sulfide.
[Biological Activity]

Novel positive allosteric modulator of GABA B receptor function. Potentiates the effects of GABA on [ 35 S]GTP γ S binding at recombinant and native GABA B receptors (EC 50 values are 2.1 and 3.1 μ M respectively). Decreases cocaine self-administration, blocks the rewarding properties of nicotine and produces anxiolytic-like activity without the side effects associated with baclofen or benzodiazepines.
[storage]

Store at RT
Spectrum DetailBack Directory
[Spectrum Detail]

GS 39783(39069-52-8)1HNMR
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