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105565-55-7

105565-55-7 Structure

105565-55-7 Structure
IdentificationBack Directory
[Name]

ALPHA-(4-FLUOROPHENYL)-4-(5-FLUORO-2-PYRIMIDINYL)-1-PIPERAZINEBUTANOL HYDROCHLORIDE
[CAS]

105565-55-7
[Synonyms]

BMS-181100
BMY-14802-1
BMY14802HyClHCl
BMY 14802 HYDROCHLORIDE
α-(4-Fluorophenyl)-4-(5-fluoro-2-pyrimidinyl)-1-piperazinebutanolhydrochloride
ALPHA-(4-FLUOROPHENYL)-4-(5-FLUORO-2-PYRIMIDINYL)-1-PIPERAZINEBUTANOL HYDROCHLORIDE
[Molecular Formula]

C18H23ClF2N4O
[MDL Number]

MFCD04039786
[MOL File]

105565-55-7.mol
[Molecular Weight]

384.85
Chemical PropertiesBack Directory
[storage temp. ]

Desiccate at RT
[solubility ]

<9.62mg/ml in H2O
[form ]

solid
[color ]

White
Hazard InformationBack Directory
[Uses]

BMY 14802 Hydrochloride was studied to be a potential atypical antipsychotic agent.
[Biological Activity]

Potent sigma receptor antagonist (IC 50 = 112 nM) with modest to weak affinity for 5-HT 1A and α 1 receptors. Antipsychotic following oral administration and acts via indirect modulation of central dopaminergic systems.
[in vitro]

bmy 14802 has its most potent binding at the sigma binding site, with some degree of serotonin subtype 1a and negligible dopamine receptor binding [1].
[in vivo]

bmy 14802 is atypical of standard neuroleptics in that it does not induce catalepsy in rats. in addition, it has been shown to have efficacy in animal models of psychosis [1].
[IC 50]

112 nm for (+)-[3h]-3-ppp
[References]

[1] gewirtz gr, gorman jm, volavka j, macaluso j, gribkoff g, taylor dp, borison r. bmy 14802, a sigma receptor ligand for the treatment of schizophrenia. neuropsychopharmacology. 1994 feb;10(1):37-40.
Spectrum DetailBack Directory
[Spectrum Detail]

ALPHA-(4-FLUOROPHENYL)-4-(5-FLUORO-2-PYRIMIDINYL)-1-PIPERAZINEBUTANOL HYDROCHLORIDE(105565-55-7)1HNMR
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