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Chlorprothixene hydrochloride

Name: Chlorprothixene hydrochloride
Brand: SIGMA

Synonym(s):

2-Chloro-9-(3-dimethylaminopropylidene)thioxanthene hydrochloride

About This Item

Empirical Formula (Hill Notation):

C₁₈H₁₈ClNS · HCl

CAS Number:

6469-93-8

Molecular Weight:

352.32

NACRES:

NA.77

PubChem Substance ID:

24278300

UNSPSC Code:

12352200

EC Number:

229-289-3

MDL number:

MFCD01941605

Form:

powder

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Properties

form

powder

storage temp.

2-8°C

SMILES string

Cl.CN(C)CC\C=C1\c2ccccc2Sc3ccc(Cl)cc13

InChI

1S/C18H18ClNS.ClH/c1-20(2)11-5-7-14-15-6-3-4-8-17(15)21-18-10-9-13(19)12-16(14)18;/h3-4,6-10,12H,5,11H2,1-2H3;1H/b14-7-;

InChI key

YWKRLOSRDGPEJR-KIUKIJHYSA-N

Gene Information

human ... DRD2(1813), DRD3(1814), HTR2A(3356), HTR2C(3358)

Description

General description

Chlorprothixene is a neuroleptic drug, which belongs to thioxanthene group. It has anticholinergic effects. Chlorprothixene might be associated with obstructive jaundice and parkinsonism. It is used to treat psychosis.

Application

Chlorprothixene hydrochloride has been used to study its exposure effects on learning and memory of rats.

Biochem/physiol Actions

D₂ dopamine receptor antagonist; blocks a subset of GABA_A receptors in rat cortex that is also blocked by clozapine; thioxanthine antipsychotic.

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This Item	C1915000	P4670	E5406
Sigma-Aldrich C1671 Chlorprothixene hydrochloride	C1915000 Chlorprothixene hydrochloride	Sigma-Aldrich P4670 Propafenone hydrochloride	Sigma-Aldrich E5406 Ethopropazine hydrochloride
form powder	form -	form powder	form powder
storage temp. 2-8°C	storage temp. 2-8°C	storage temp. 2-8°C	storage temp. 2-8°C
Gene Information human ... DRD2(1813), DRD3(1814), HTR2A(3356), HTR2C(3358)	Gene Information human ... DRD2(1813), DRD3(1814), HTR2A(3356), HTR2C(3358)	Gene Information human ... ABCB1(5243), ADRB1(153), ADRB2(154), ADRB3(155), CYP1A2(1544), SCN10A(6336), SCN11A(11280), SCN1A(6323), SCN2A(6326), SCN3A(6328), SCN4A(6329), SCN5A(6331), SCN7A(6332), SCN8A(6334), SCN9A(6335)	Gene Information human ... CHRM1(1128)

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pictograms

GHS06

signalword

Danger

hcodes

H301

pcodes

P301 + P310

Hazard Classifications

Acute Tox. 3 Oral

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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Meyler's Side Effects of Drugs: The International Encyclopedia of Adverse Drug Reactions and Interactions (2015)

Distinct in vivo dynamics of excitatory synapses onto cortical pyramidal neurons and parvalbumin-positive interneurons.

Joshua B Melander et al.

Cell reports, 37(6), 109972-109972 (2021-11-11)

Cortical function relies on the balanced activation of excitatory and inhibitory neurons. However, little is known about the organization and dynamics of shaft excitatory synapses onto cortical inhibitory interneurons. Here, we use the excitatory postsynaptic marker PSD-95, fluorescently labeled at

Biologically active conformers of phenothiazines and thioxanthenes. Further evidence for a ligand model of dopamine D2 receptor antagonists.

M Froimowitz et al.

Journal of medicinal chemistry, 36(15), 2219-2227 (1993-07-23)

Conformational analyses have been performed on several phenothiazine and thioxanthene dopamine antagonists using the MM2-87 program and parameter set. The compounds that were examined are thioridazine (2), methotrimeprazine (3), cis- and trans-chlorprothixene, and a piperidylidene derivative of chlorprothixene. In addition

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Global Trade Item Number

SKU	GTIN
C1671-1G	04061825982038

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