General
Preferred name
FLUPHENAZINE DIHYDROCHLORIDE
Synonyms
FLUPHENAZINE HYDROCHLORIDE ()
Fluphenazine (HCl) ()
Prolixin ()
Fluphenazine (dihydrochloride) ()
NSC-179197 ()
Moditen ()
Anatensol ()
Fluphenazine HCl ()
SQUIBB 4918 ()
Fluphenazine dihydrochloride ()
Permitil ()
Dapotum ()
Fluphenazini hydrochloridum ()
P&D ID
PD001518
CAS
146-56-5
Tags
available
drug
nuisance
Drug Status
approved
Max Phase
4.0
Drug indication
Multiple myeloma
First approval
1959
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
PRICE 29
DESCRIPTION Fluphenazine dihydrochloride is a phenothiazine-class D1DR and D2DR inhibitor. It also inhibits Histamine H1 Receptor. (Enamine Bioactive Compounds)
DESCRIPTION Dopamine receptor antagonist; antipsychotic (LOPAC library)
DESCRIPTION Fluphenazine dihydrochloride (Prolixin) is an inhibitor of phenothiazine-class D1DR and D2DR; In studies, Fluphenazine can be used to probe the effects and metabolic process of this commonly used dopamine antagonist. (TargetMol Bioactive Compound Library)
Cell lines
0
Organisms
2
Compound Sets
12
ChEMBL Approved Drugs
ChEMBL Drugs
CZ-OPENSCREEN Bioactive Library
Enamine Bioactive Compounds
Enamine BioReference Compounds
LOPAC library
MedChem Express Bioactive Compound Library
Nuisance compounds in cellular assays
Prestwick Chemical Library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
The Spectrum Collection
External IDs
22
Properties
(calculated by RDKit )
Molecular Weight
509.13
Hydrogen Bond Acceptors
5
Hydrogen Bond Donors
1
Rotatable Bonds
6
Ring Count
4
Aromatic Ring Count
2
cLogP
5.15
TPSA
29.95
Fraction CSP3
0.45
Chiral centers
0.0
Largest ring
6.0
QED
0.58
Structural alerts
1
CAD
Nuisance compounds
Custom attributes
(extracted from source data)
Selectivity
D1/D2
Target
dopamine
Dopamine Receptor
SARS-CoV
Sodium Channel
Pathway
Anti-infection
GPCR/G protein
Membrane Transporter/Ion Channel
Neuronal Signaling
Neuroscience
Source data