ChemicalBook--->CAS DataBase List--->1210-81-7

1210-81-7

1210-81-7 Structure

1210-81-7 Structure
IdentificationBack Directory
[Name]

2-(5-chloro-2-methyl-1H-indol-3-yl)-N,N-dimethylethanamine
[CAS]

1210-81-7
[Synonyms]

ST1936
ST1936,ST-1936
ST 1936 oxalate
1H-Indole-3-ethanamine, 5-chloro-N,N,2-trimethyl-
5-Chloro-3-[2-(dimethylamino)ethyl]-2-methylindole oxalate
2-(5-chloro-2-methyl-1H-indol-3-yl)-N,N-dimethylethanamine
[Molecular Formula]

C13H17ClN2
[MDL Number]

MFCD22201006
[MOL File]

1210-81-7.mol
[Molecular Weight]

236.74
Chemical PropertiesBack Directory
[Boiling point ]

377.0±42.0 °C(Predicted)
[density ]

1.165±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: ≥5mg/mL (warmed)
[form ]

powder
[pka]

16.90±0.30(Predicted)
[color ]

white to beige
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Serotonin 5-HT(6) receptor agonists and antagonists have been proposed as possible useful compounds in the treatment of psychiatric disorders such as depression (1). ST 1936 Oxalate is a 5-HT(6) receptor agonist and may be a potential antidepressant/anti-anhedonic drug (1,2).
[in vivo]

ST1936 (5, 10, 20 mg/kg; i.p.) increases in a dose dependent manner extracellular dopamine (DA) and NA levels in the prefrontal cortex (PFCX)[4].
ST1936 (5, 10, 20 mg/kg; i.p.) increases extracellular DA and NA levels in the nucleus accumbens (NAc) core. Doses of 10 mg/kg increases dialysate DA (peak: 179%) while higher dose increases both DA and NA dialysates (201% and 231%, respectively). Doses of 5 mg/kg does not produce any effect[4].

[IC 50]

5-HT6 Receptor: 13 nM (Ki); 5-HT7 Receptor: 168 nM (Ki); 5-HT2B Receptor: 245 nM (Ki); α1-adrenergic receptor: 390 nM (Ki, rat); α2-adrenergic receptor: 300 nM (Ki, rat); α2-adrenergic receptor: 300 nM (Ki, human)
Spectrum DetailBack Directory
[Spectrum Detail]

2-(5-chloro-2-methyl-1H-indol-3-yl)-N,N-dimethylethanamine(1210-81-7)1HNMR
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