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SB-200646

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
SB-200646
Clinical data
ATC code
  • none
Legal status
Legal status
Identifiers
  • 1-(1-Methyl-1H-indol-5-yl)-3-pyridin-3-ylurea
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC15H14N4O
Molar mass266.304 g·mol−1
3D model (JSmol)
  • Cn1ccc2c1ccc(c2)NC(=O)Nc3cccnc3
  • 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 a5-HT2receptor antagonist withanxiolytic properties in rats. It was the first 5-HT2 antagonist discovered to exhibit selectivity for the5-HT2C/2B receptors over the5-HT2A receptor.[1]

References

[edit]
  1. ^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.
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
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