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52669-92-8

52669-92-8 Structure

52669-92-8 Structure
IdentificationBack Directory
[Name]

4(4-chlorophenyl)-1-(4-(4-fluorophenyl)-4-oxobutyl)-1,2,3,6-tetrahydropyridine hydrochloride
[CAS]

52669-92-8
[Synonyms]

HPTP
HLPR
HPTPA
RPTPA
PTPRS
R-PTP-α
Dehydrated Haloperidol
Haloperidol Impurity 43
PTPsigma/PTPRS Active human
PTPRA (174-802), active, GST tagged human
Haloperidol Impurity 9(Dehydrate Haloperidol)
Protein tyrosine phosphatase, receptor type, S
1-[4-Oxo-4-(4-fluorophenyl)butyl]-4-(4-chlorophenyl)-1,2,3,6-tetrahydropyridine
4-[4-(4-Chlorophenyl)-3,6-dihydro-1(2H)-pyridinyl]-1-(4-fluorophenyl)-1-butanone
4-[4-(4-chlorophenyl)-3,6-dihydro-2H-pyridin-1-yl]-1-(4-fluorophenyl)butan-1-one
1-Butanone, 4-[4-(4-chlorophenyl)-3,6-dihydro-1(2H)-pyridinyl]-1-(4-fluorophenyl)-
4-[[4-(4-Chlorophenyl)-1,2,3,6-tetrahydropyridin]-1-yl]-1-(4-fluorophenyl)-1-butanone
4(4-chlorophenyl)-1-(4-(4-fluorophenyl)-4-oxobutyl)-1,2,3,6-tetrahydropyridine hydrochloride
[Molecular Formula]

C21H21ClFNO
[MDL Number]

MFCD28252198
[MOL File]

52669-92-8.mol
[Molecular Weight]

357.85
Chemical PropertiesBack Directory
[Melting point ]

97 - 100°C
[density ]

1.196
[storage temp. ]

-70°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

aqueous solution
[color ]

Pale Yellow
[biological source]

human
[Specific Activity]

1799-2435nmol/min·mg
Safety DataBack Directory
[Symbol(GHS) ]


GHS08,GHS06
[Signal word ]

Danger
[Hazard statements ]

H315-H317-H360-H335-H319-H301
[Precautionary statements ]

P261-P272-P280-P302+P352-P333+P313-P321-P363-P501-P264-P270-P301+P310-P321-P330-P405-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
Hazard InformationBack Directory
[Uses]

4-[4-(4-Chlorophenyl)-3,6-dihydro-1(2H)-pyridinyl]-1-(4-fluorophenyl)-1-butanone is a dehydrated metabolite of haloperidol that can be biotransfomed by humans to Haloperidol pyridinium (HPP+), a potential neurotoxic found in the brain.
[Definition]

ChEBI: 4-(4-(P-Chlorophenyl)-2,5,6-Trihydropyridino)-4'-Fluorobutyrophenone is an aromatic ketone.
[Biological Activity]

Protein tyrosine phosphatasereceptor type S (PTPRS)/ PTPs localized on the cell surface plays a vital role in cell–cell and cell– extracellular matrix (ECM) interactionsand is implicated in the regulation of axon homeostasis and neuronal development. In additionPTPRS also has a crucial role in autophagy regulation. PTPRS expressed on plasmacytoid dendritic cells (pDCs) inhibits the production of type I interferon (IFN) in response to viruses. Mutation of both Ptprs and Ptprf (protein tyrosine phosphatasereceptor type F) results in pDC hyperactivation and mild colitis.
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