ChemicalBook--->CAS DataBase List--->143797-63-1

143797-63-1

143797-63-1 Structure

143797-63-1 Structure
IdentificationBack Directory
[Name]

SB 200646 HYDROCHLORIDE
[CAS]

143797-63-1
[Synonyms]

SB 200646
SB200646HCl
SB 200646 HYDROCHLORIDE
N-(1-methyl-5-indolyl)-N'-(3-pyridyl)urea
N-(1-Methyl-1H-indol-5-yl)-N'-3-pyridinylurea
1-(1-Methyl-1H-indol-5-yl)-3-pyridin-3-yl-urea
Urea, N-(1-methyl-1H-indol-5-yl)-N'-3-pyridinyl-
N-(1-METHYL-1H-INDOL-5-YL)-N'-3-PYRIDINYLUREA HYDROCHLORIDE
N-(1-METHYL-1H-5-INDOLYL)-N'-(3-PYRIDINYL)UREA HYDROCHLORIDE
[Molecular Formula]

C15H14N4O
[MOL File]

143797-63-1.mol
[Molecular Weight]

266.3
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

DMSO: ~26 mg/mL, soluble
[form ]

solid
[color ]

pale yellow
[Water Solubility ]

Water: 1 mg/mL (NaN mM)
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[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.
[Definition]

ChEBI: SB 200646 is a member of indoles.
[Biological Activity]

5-HT 2C/2B receptor antagonist, selective over 5-HT 1A . Affinities are 7.4 (pA 2 ), 6.9 (pK i ) and 5.2 (pK i ) for 5-HT 2B , 2C and 2A respectively. Orally active in vivo .
[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)
Spectrum DetailBack Directory
[Spectrum Detail]

SB 200646 HYDROCHLORIDE(143797-63-1)1HNMR
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