SB-200646

SB-200646
Clinical data
ATC code	none;
Legal status
Legal status	UN: Unscheduled;
Identifiers
	IUPAC name 1-(1-Methyl-1H-indol-5-yl)-3-pyridin-3-ylurea;
CAS Number	143797-63-1 ;
PubChem CID	126769;
ChemSpider	112592;
KEGG	C11739;
ChEBI	CHEBI:8976;
ChEMBL	ChEMBL85194;
CompTox Dashboard (EPA)	DTXSID40162550 ;
Chemical and physical data
Formula	C15H14N4O
Molar mass	266.304 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES Cn1ccc2c1ccc(c2)NC(=O)Nc3cccnc3;
	InChI InChI=1S/C15H14N4O/c1-19-8-6-11-9-12(4-5-14(11)19)17-15(20)18-13-3-2-7-16-10-13/h2-10H,1H3,(H2,17,18,20); Key:OJZZJTLBYXHUSJ-UHFFFAOYSA-N;

SB-200646 is a 5-HT₂ receptor antagonist with anxiolytic properties in rats. It was the first 5-HT₂ antagonist discovered to exhibit selectivity for the 5-HT_2C/_2B receptors over the 5-HT_2A receptor.^[1]

References

^ Kennett GA, Wood MD, Glen A, Grewal S, Forbes I, Gadre A, Blackburn TP (March 1994). "In vivo properties of SB 200646A, a 5-HT2C/2B receptor antagonist". British Journal of Pharmacology. 111 (3): 797–802. doi:10.1111/j.1476-5381.1994.tb14808.x. PMC 1910094. PMID 7912626.

Clinical data

ATC code	none
Legal status
Legal status	UN: Unscheduled
Identifiers
IUPAC name 1-(1-Methyl-1H-indol-5-yl)-3-pyridin-3-ylurea
CAS Number	143797-63-1^Y
PubChem CID	126769
ChemSpider	112592
KEGG	C11739
ChEBI	CHEBI:8976
ChEMBL	ChEMBL85194
CompTox Dashboard (EPA)	DTXSID40162550
Chemical and physical data
Formula	C₁₅H₁₄N₄O
Molar mass	266.304 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES Cn1ccc2c1ccc(c2)NC(=O)Nc3cccnc3
InChI InChI=1S/C15H14N4O/c1-19-8-6-11-9-12(4-5-14(11)19)17-15(20)18-13-3-2-7-16-10-13/h2-10H,1H3,(H2,17,18,20) Key:OJZZJTLBYXHUSJ-UHFFFAOYSA-N