ChemicalBook--->CAS DataBase List--->143797-62-0

143797-62-0

143797-62-0 Structure

143797-62-0 Structure
IdentificationBack Directory
[Name]

SB 200646 HYDROCHLORIDE
[CAS]

143797-62-0
[Synonyms]

SB-200646A
[Molecular Formula]

C15H14N4O.ClH
[MDL Number]

MFCD00913519
[MOL File]

143797-62-0.mol
[Molecular Weight]

302.763
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

DMSO: ~26 mg/mL, soluble
[form ]

solid
[color ]

pale yellow
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H315-H319
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

SB 200646 Hydrochloride is a 5-HT2C antagonist.
[in vivo]

SB-200646A (20 mg/kg; intravenous injection; daily; for 21 days; male albino Sprague-Dawley rats) treatment significantly decreases the number of spontaneously active ventral tegmental area (VTA) dopaminergic neurons[1].
The i.v. administration of 4-16 mg/kg of SB-200646A significantly increases the firing rate and % events as bursts in spontaneously active VTA dopaminergic neurons and significantly increases the % events as burst in substantia nigra pars compacta (SNC) dopaminergic neurons[1].

Animal Model:Male albino Sprague-Dawley rats (200-225 g at the beginning of treatment and 300-350 g at the time of the experiment)[1]
Dosage:20 mg/kg
Administration:Intravenous injection; daily; for 21 days
Result:Significantly decreased the number of spontaneously active ventral tegmental area (VTA) dopaminergic neurons.
[IC 50]

5-HT2B Receptor: 7.5 (pKi); 5-HT2C Receptor: 6.9 (pKi); 5-HT2A Receptor: 5.2 (pKi)
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