Jump to content

SB-649,915

From Wikipedia, the free encyclopedia
(Redirected fromSB-649915)
SB-649,915
Clinical data
ATC code
  • none
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • 6-[(1-[3-(2-methylquinolin-5-yl)oxypropyl]piperidin-4-yl)methyl]-4H-1,4-benzoxazin-3-one
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC26H29N3O3
Molar mass431.536g·mol−1
3D model (JSmol)
  • O=C4COc1ccc(cc1N4)CC(CC5)CCN5CCOc(cccc2n3)c2ccc3C
  • InChI=1S/C26H29N3O3/c1-18-5-7-21-22(27-18)3-2-4-24(21)31-14-13-29-11-9-19(10-12-29)15-20-6-8-25-23(16-20)28-26(30)17-32-25/h2-8,16,19H,9-15,17H2,1H3,(H,28,30)☒N
  • Key:PJSUYRBCBFPCQW-UHFFFAOYSA-N☒N
☒NcheckY(what is this?)(verify)

SB-649,915is aserotonin reuptake inhibitorand5-HT1Aand5-HT1Breceptorantagonistwhich is being investigated for itsantidepressanteffects.[1]Relative to theselective serotonin reuptake inhibitors(SSRIs), SB-649,915 has a fasteronset of actionand may also have greater clinical efficacy as well.[1]This can be attributed to blockade of 5-HT1Aand 5-HT1Bautoreceptorswhich inhibitserotoninrelease.[1]

See also

[edit]

References

[edit]
  1. ^abcStarr KR, Price GW, Watson JM, Atkinson PJ, Arban R, Melotto S, Dawson LA, Hagan JJ, Upton N, Duxon MS (2007)."SB-649915-B, a novel 5-HT1A/B autoreceptor antagonist and serotonin reuptake inhibitor, is anxiolytic and displays fast onset activity in the rat high light social interaction test".Neuropsychopharmacology.32(10): 2163–2172.doi:10.1038/sj.npp.1301341.PMID17356576.