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Fluphenazine dihydrochloride

Name: Fluphenazine dihydrochloride
Brand: SIGMA

Synonym(s):

4-[3-[2-(Trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-1-piperazineethanol dihydrochloride

About This Item

Empirical Formula (Hill Notation):

C₂₂H₂₆F₃N₃OS · 2HCl

CAS Number:

146-56-5

Molecular Weight:

510.44

NACRES:

NA.77

PubChem Substance ID:

57654184

UNSPSC Code:

12352200

EC Number:

205-674-1

MDL number:

MFCD00055212

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SMILES string

Cl.Cl.OCCN1CCN(CCCN2c3ccccc3Sc4ccc(cc24)C(F)(F)F)CC1

InChI

1S/C22H26F3N3OS.2ClH/c23-22(24,25)17-6-7-21-19(16-17)28(18-4-1-2-5-20(18)30-21)9-3-8-26-10-12-27(13-11-26)14-15-29;;/h1-2,4-7,16,29H,3,8-15H2;2*1H

InChI key

MBHNWCYEGXQEIT-UHFFFAOYSA-N

Gene Information

human ... DRD1(1812), DRD2(1813), HRH1(3269)

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General description

Fluphenazine may be useful for the treatment of schizophrenia.

Application

Fluphenazine dihydrochloride has been used:

to study its effects as a drug on glioblastoma (GBM) cells
in fluorescence-activated cell sorting (FACS) analysis, sorting and single-cell stress-survival experiments
to study its exposure effects on learning and memory in adult rats

Biochem/physiol Actions

D₁/D₂ dopamine receptor antagonist; phenothiazine antipsychotic; H₁ histamine receptor antagonist.

pictograms

GHS06,GHS08

signalword

Danger

hcodes

H301,H360

pcodes

P201 - P301 + P310 + P330

Hazard Classifications

Acute Tox. 3 Oral - Repr. 1A

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Principles of Psychopharmacology for Mental Health Professionals (2006)

Coupling phenotypic persistence to DNA damage increases genetic diversity in severe stress

Yaakov G, et al.

Nature ecology & evolution, 1(1), 0016-0016 (2017)

Inverse agonist properties of dopaminergic antagonists at the D(1A) dopamine receptor: uncoupling of the D(1A) dopamine receptor from G(s) protein.

G Cai et al.

Molecular pharmacology, 56(5), 989-996 (1999-10-26)

The interaction of dopaminergic antagonists with the D(1A) dopamine receptor was assessed in PC2 cells that transiently express this receptor. The maximal binding and dissociation constants for the D(1A) dopamine receptor, using the ligand [(125)I]SCH23982 were 0.38 +/- 0.09 nM

The Effect of Intrauterine Antipsychotic Drug Exposure on Learning and Memory in Adult Rats

Oltulu C and Karadag CH

Klinik Psikofarmakoloji Bulteni-Bulletin of Clinical Psychopharmacology, 26(4), 364-373 (2016)

Identification of thioridazine, an antipsychotic drug, as an antiglioblastoma and anticancer stem cell agent using public gene expression data

Cheng HW, et al.

Cell Death & Disease, 6(5), e1753-e1753 (2015)

View All Related Papers

Global Trade Item Number

SKU	GTIN
F4765-1G	04061825982250
F4765-5G	04061832090832

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