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Details

Stereochemistry ACHIRAL
Molecular Formula C24H27ClN2O2S
Molecular Weight 443.001
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of ZUCLOPENTHIXOL ACETATE

SMILES

CC(=O)OCCN1CCN(CC\C=C2\C3=C(SC4=C2C=C(Cl)C=C4)C=CC=C3)CC1

InChI

InChIKey=OXAUOBQMCDIVPQ-IOXNKQMXSA-N
InChI=1S/C24H27ClN2O2S/c1-18(28)29-16-15-27-13-11-26(12-14-27)10-4-6-20-21-5-2-3-7-23(21)30-24-9-8-19(25)17-22(20)24/h2-3,5-9,17H,4,10-16H2,1H3/b20-6-

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including https://www.lundbeck.com/upload/au/files/pdf/Clopixol_CMI.pdf | https://www.ncbi.nlm.nih.gov/pubmed/26624987

Zuclopenthixol is indicated the management of the manifestations of schizophrenia and other mental illnesses with disturbances in thinking, emotional reactions and behaviour. It is also used to treat the manic phase of manic depressive illness. Zuclopenthixol, a thioxanthene derivative, has high affinity for both dopamine D1 receptors and dopamine D2 receptors. Zuclopenthixol also has high affinity for α1-adrenergic and 5-HT2 receptors. Zuclopenthixol (CLOPIXOL®) is avavilable in the form of tablets and solution for intramuscular injections.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
CLOPIXOL

Approved Use

Zuclopenthixol is indicated the management of the manifestations of schizophrenia and other mental illnesses with disturbances in thinking, emotional reactions and behaviour. It is also used to treat the manic phase of manic depressive illness.
Primary
CLOPIXOL

Approved Use

Zuclopenthixol is indicated the management of the manifestations of schizophrenia and other mental illnesses with disturbances in thinking, emotional reactions and behaviour. It is also used to treat the manic phase of manic depressive illness.
PubMed

PubMed

TitleDatePubMed
The bucco-linguo-masticatory syndrome as a side-effect of neuroleptics therapy.
1967
The antibacterial effect of selected phenothiazines and thioxanthenes on slow-growing mycobacteria.
1986 Dec
Prolonged oculogyric crisis on addition of nifedipine to neuroleptic medication regime.
1987 Jan
Zuclopenthixol and perphenazine in patients with acute psychotic states. A double-blind multicentre study.
1987 Jul
Zuclopenthixol and haloperidol/levomepromazine in the treatment of elderly patients with symptoms of aggressiveness and agitation: a double-blind, multi-centre study.
1989
Zuclopenthixol, a combined dopamine D1/D2 antagonist, versus haloperidol, a dopamine D2 antagonist, in tardive dyskinesia.
1991 Dec
[acute dystonias in combined abuse of cocaine and neuroleptics].
1994 Nov 26
Long term results of unilateral posteroventral pallidotomy for antipsychotic drug induced tardive dyskinesia.
2005 Jul
[Trazodone for the treatment of behavioral and psychological symptoms of dementia (BPSD) in Alzheimer's disease: a retrospective study focused on the aggression and negativism in caregiving situations].
2006 Jun
Fatal exertional heat stroke in a patient receiving zuclopenthixol, quetiapine and benztropine.
2007 Fall
Remission of schizophrenia psychosis and strong reduction of obsessive-compulsive disorder after adding clozapine to aripiprazole.
2009 Nov 13
Severe laryngeal dystonia in a patient receiving zuclopenthixol "Acuphase" and fluoxetine.
2010 Apr
Zuclopenthixol acetate for acute schizophrenia and similar serious mental illnesses.
2012 Apr 18
Simultaneous determination of 25 common pharmaceuticals in whole blood using ultra-performance liquid chromatography-tandem mass spectrometry.
2012 Sep
Patents

Sample Use Guides

Clopixol tablets: The usual dose is 10 to 50 mg per day. Clopixol Acuphase injection: The usual dose is 50 to 150 mg (1 to 3 mL) every 2 to 3 days or as instructed by your doctor. Clopixol Depot injection: The usual dose is 200 to 400 mg (1 to 2 mL) every second to fourth week.
Route of Administration: Other
In Vitro Use Guide
Unknown
Name Type Language
ZUCLOPENTHIXOL ACETATE
MART.   WHO-DD  
Common Name English
ZUCLOPENTHIXOL ACETATE [MART.]
Common Name English
Zuclopenthixol acetate [WHO-DD]
Common Name English
(Z)-4-(3-(2-CHLOROTHIOXANTHEN-9-YLIDENE)PROPYL)-1-PIPERAZINEETHANOL ACETATE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29710
Created by admin on Fri Dec 15 18:17:56 GMT 2023 , Edited by admin on Fri Dec 15 18:17:56 GMT 2023
Code System Code Type Description
FDA UNII
349S2ZHF05
Created by admin on Fri Dec 15 18:17:56 GMT 2023 , Edited by admin on Fri Dec 15 18:17:56 GMT 2023
PRIMARY
CAS
85721-05-7
Created by admin on Fri Dec 15 18:17:56 GMT 2023 , Edited by admin on Fri Dec 15 18:17:56 GMT 2023
PRIMARY
EVMPD
SUB05195MIG
Created by admin on Fri Dec 15 18:17:56 GMT 2023 , Edited by admin on Fri Dec 15 18:17:56 GMT 2023
PRIMARY
MESH
C060342
Created by admin on Fri Dec 15 18:17:56 GMT 2023 , Edited by admin on Fri Dec 15 18:17:56 GMT 2023
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DRUG CENTRAL
4075
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PUBCHEM
6436640
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DRUG BANK
DBSALT000545
Created by admin on Fri Dec 15 18:17:56 GMT 2023 , Edited by admin on Fri Dec 15 18:17:56 GMT 2023
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EPA CompTox
DTXSID00235032
Created by admin on Fri Dec 15 18:17:56 GMT 2023 , Edited by admin on Fri Dec 15 18:17:56 GMT 2023
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RXCUI
58338
Created by admin on Fri Dec 15 18:17:56 GMT 2023 , Edited by admin on Fri Dec 15 18:17:56 GMT 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
288-415-5
Created by admin on Fri Dec 15 18:17:56 GMT 2023 , Edited by admin on Fri Dec 15 18:17:56 GMT 2023
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NCI_THESAURUS
C95835
Created by admin on Fri Dec 15 18:17:56 GMT 2023 , Edited by admin on Fri Dec 15 18:17:56 GMT 2023
PRIMARY
SMS_ID
100000088298
Created by admin on Fri Dec 15 18:17:56 GMT 2023 , Edited by admin on Fri Dec 15 18:17:56 GMT 2023
PRIMARY