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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

Molecular Formula C24H27ClN2O2S
Molecular Weight 443.001
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

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 antibacterial effect of selected phenothiazines and thioxanthenes on slow-growing mycobacteria.
1986 Dec
Reversible lithium neurotoxicity at normal serum level may refer to intracranial pathology.
1989 May
[acute dystonias in combined abuse of cocaine and neuroleptics].
1994 Nov 26
Antipsychotic-induced extrapyramidal syndromes. Risperidone compared with low- and high-potency conventional antipsychotic drugs.
2001 Jul
Clozapine and weight gain.
2001 May
Pro-oxidant activity of zuclopenthixol in vivo: differential effect of the drug on brain oxidative status of scopolamine-treated rats.
2004 Aug
Long term results of unilateral posteroventral pallidotomy for antipsychotic drug induced tardive dyskinesia.
2005 Jul
Remission of schizophrenia psychosis and strong reduction of obsessive-compulsive disorder after adding clozapine to aripiprazole.
2009 Nov 13
Zuclopenthixol acetate for acute schizophrenia and similar serious mental illnesses.
2012 Apr 18
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
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:17:56 GMT 2023
Edited
by admin
on Fri Dec 15 18:17:56 GMT 2023
Record UNII
349S2ZHF05
Record Status Validated (UNII)
Record Version
  • Download
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
PRIMARY
DRUG CENTRAL
4075
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
PUBCHEM
6436640
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
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
PRIMARY
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
PRIMARY
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
PRIMARY
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
Related Record Type Details
ACTIVE MOIETY