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ChemicalBook--->CAS DataBase List--->903580-39-2

903580-39-2

903580-39-2 Structure

903580-39-2 Structure
IdentificationBack Directory
[Name]

PRX 07034
[CAS]

903580-39-2
[Synonyms]

PRX 07034
N-[1-(5-chloro-2,3-dimethoxyphenyl)ethyl]-2-methylsulfonyl-5-piperazin-1-ylaniline:hydrochloride
Benzenemethanamine, 5-chloro-2,3-dimethoxy-α-methyl-N-[2-(methylsulfonyl)-5-(1-piperazinyl)phenyl]-, hydrochloride
Benzenemethanamine, 5-chloro-2,3-dimethoxy-α-methyl-N-[2-(methylsulfonyl)-5-(1-piperazinyl)phenyl]-, monohydrochloride
[Molecular Formula]

C21H28ClN3O4S.ClH
[MDL Number]

MFCD25976674
[MOL File]

903580-39-2.mol
[Molecular Weight]

490.45
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

PRX-07034 hydrochloride is a highly selective and potent 5-HT6 receptor antagonist with a Ki= 4-8 nM and an IC50 of 19 nM. PRX-07034 can be used for the research of enhancing working memory and cognitive flexibility[1].
[in vivo]

PRX-07034 (0.1, 1, or 3 mg/kg; i.p.; 30 min prior to delayed spontaneous alternation testing) selectively enhances a switch to a place discrimination[1].

Animal Model:Male Long-Evans rats weighing approximately 350 g[1]
Dosage:0.1, 1, or 3 mg/kg
Administration:Injected intraperitoneal
Result:1 and 3 mg/kg (but not 0.1 mg/kg) significantly enhanced delayed spontaneous alternation. The drug at 1 and 3 mg/kg also enhanced switching between a place and response strategy, but did not affect initial learning of either a place or response discrimination.
[IC 50]

5-HT6 Receptor: 4-8 nM (Ki); 5-HT6 Receptor: 19 nM (IC50); 5-HT1B Receptor: 260 nM (Ki); 5-HT1A Receptor: 420 nM (Ki); 5-HT1D Receptor: 2.8 μM (Ki); 5-HT2A Receptor: 2.5 μM (IC50); 5-HT2B Receptor: 2.5 μM (IC50); 5-HT2C Receptor: 3.7 μM (IC50); Dopamine D3 Receptor: 71 nM (Ki); Opioid μ Receptor: 0.45 μM (Ki); Histamine H2 Receptor: 0.64 μM (Ki)
[storage]

Store at -20°C
[References]

[1] Eric G Mohler, et al. The effects of PRX-07034, a novel 5-HT6 antagonist, on cognitive flexibility and working memory in rats. Psychopharmacology (Berl). 2012 Apr;220(4):687-96. DOI:10.1007/s00213-011-2518-7
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