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554403-08-6

554403-08-6 Structure

554403-08-6 Structure
IdentificationBack Directory
[Name]

2-[1-[(6-Chloroimidazo[2,1-b][1,3]thiazol-5-yl)sulfonyl]-1H-indol-3-yl]ethylamine Hydrochloride
[CAS]

554403-08-6
[Synonyms]

SAX-187 hydrochloride
2-[1-(6-chloroimidazo[2,1-b][1,3]thiazol-5-yl)sulfonylindol-3-yl]ethanamine
hydrochloride 1H-Indole-3-ethanamine, 1-((6-chloroimidazo((2,1-b)thiazol-5-yl)sulfonyl)-, hydrochloride (1:1)
[Molecular Formula]

C15H14Cl2N4O2S2
[MDL Number]

MFCD29907475
[MOL File]

554403-08-6.mol
[Molecular Weight]

417.32
Hazard InformationBack Directory
[Uses]

2-[1-[(6-Chloroimidazo[2,1-b][1,3]thiazol-5-yl)sulfonyl]-1H-indol-3-yl]ethylamine Hydrochloride is the HCl salt of 2-[1-[(6-Chloroimidazo[2,1-b][1,3]thiazol-5-yl)sulfonyl]-1H-indol-3-yl]ethylamine which is a selective 5-HT6 receptor agonist. It has been proven to have antidepressant and anxiolytic effects on rats suggesting its usefulness as a potential antidepressant.
[in vivo]

Acute administration of WAY-181187 (3-30 mg/kg, s.c.) hydrochloride significantly increases extracellular GABA concentrations without altering the levels of glutamate or norepinephrine in the rat frontal cortex. Additionally, WAY-181187 (30 mg/kg, s.c.) hydrochloride produces modest yet significant decreases in cortical dopamine and 5-HT levels[1].

Animal Model:Adult male Sprague-Dawley rats weighing 280-350 g[1]
Dosage:3, 10, or 30 mg/kg
Administration:Acute dministered by s.c.
Result:Significantly increased extracellular GABA concentrations without altering the levels of glutamate or norepinephrine.
[IC 50]

5-HT6 Receptor: 2.2 nM (Ki); 5-HT6 Receptor: 6.6 nM (EC50)
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