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276695-22-8

276695-22-8 Structure

276695-22-8 Structure
IdentificationBack Directory
[Name]

8,9-dichloro-2,3,4,4a-tetrahydro-1H-pyrazino[1,2-a]quinoxalin-5(6H)-one hydrochloride salt
[CAS]

276695-22-8
[Synonyms]

(Rac)-WAY-161503 (hydrochloride)
8,9-Dichloro-2,3,4,4a-tetrahydro-1H,6H-pyrazino[1,2-a]quinoxalin-5-one hydrochloride
8,9-dichloro-2,3,4,4a-tetrahydro-1H-pyrazino[1,2-a]quinoxalin-5(6H)-one hydrochloride salt
[Molecular Formula]

C11H12Cl3N3O
[MDL Number]

MFCD06411596
[MOL File]

276695-22-8.mol
[Molecular Weight]

308.591
Chemical PropertiesBack Directory
[storage temp. ]

room temp
[solubility ]

DMSO: >10mg/mL
[form ]

powder
[color ]

white to off-white
[InChI]

1S/C11H11Cl2N3O.ClH/c12-6-3-8-9(4-7(6)13)16-2-1-14-5-10(16)11(17)15-8;/h3-4,10,14H,1-2,5H2,(H,15,17);1H
[InChIKey]

YPNWSZJDAKOUAW-UHFFFAOYSA-N
[SMILES]

Cl.Clc1cc2NC(=O)C3CNCCN3c2cc1Cl
Safety DataBack Directory
[WGK Germany ]

nwg
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

WAY 161503 Hydrochloride is a potent serotonin 5-HT2C receptor agonist with antiobesity effects. It is the salt analogue of WAY 161503 (D437235).
[Biological Activity]

The 5-HT2C receptors have been implicated in conditions including obesityanxietydepressionOCDschizophreniamigrainenociception and erectile dysfunction.
[in vivo]

(Rac)-WAY-161503 (3-30 mg/kg; i.p.; male C57BL/6J mice) hydrochloride dose-dependently decreases locomotor activity, an effect that is blocked by the 5-HT2C/2B antagonist SER-082[1].

Animal Model:Male C57BL/6J mice with hallucinogen 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI)[1]
Dosage:3 mg/kg, 10 mg/kg, 30 mg/kg
Administration:Intraperitoneal injection (i.p.)
Result:Antagonized the PGE2-mediated inhibition of LPS-induced TNF-α release from rat whole blood culture, in a dose-dependent way.
[IC 50]

5-HT2C Receptor: 4 nM (Ki); 5-HT2C Receptor: 12 nM (EC50)
[storage]

Desiccate at RT
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