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Details

Stereochemistry ACHIRAL
Molecular Formula C32H43ClN2O2S
Molecular Weight 555.214
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of ZUCLOPENTHIXOL DECANOATE

SMILES

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

InChI

InChIKey=QRUAPADZILXULG-WKIKZPBSSA-N
InChI=1S/C32H43ClN2O2S/c1-2-3-4-5-6-7-8-15-32(36)37-24-23-35-21-19-34(20-22-35)18-11-13-27-28-12-9-10-14-30(28)38-31-17-16-26(33)25-29(27)31/h9-10,12-14,16-17,25H,2-8,11,15,18-24H2,1H3/b27-13-

HIDE SMILES / InChI

Molecular Formula C32H43ClN2O2S
Molecular Weight 555.214
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 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
Reversible lithium neurotoxicity at normal serum level may refer to intracranial pathology.
1989 May
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
Effect of some psychotropic drugs and a barbiturate on mycoplasmas.
2000 Apr
Antipsychotic-induced extrapyramidal syndromes. Risperidone compared with low- and high-potency conventional antipsychotic drugs.
2001 Jul
Clozapine and weight gain.
2001 May
Zuclopenthixol facilitates memory retrieval in rats: possible involvement of noradrenergic and serotonergic mechanisms.
2003 Jul
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
[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
Comparative analysis of anti-toxoplasmic activity of antipsychotic drugs and valproate.
2014 Mar
Paradoxical severe agitation induced by add-on high-doses quetiapine in schizo-affective disorder.
2014 May 15
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
TSS9KIZ5OG
Record Status Validated (UNII)
Record Version
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Name Type Language
ZUCLOPENTHIXOL DECANOATE
EP   MART.   WHO-DD  
Common Name English
ZUCLOPENTHIXOL DECANOATE [MART.]
Common Name English
CLOPENTHIXOL DECANOATE, CIS-
Common Name English
DECANOIC ACID, 2-(4-((3Z)-3-(2-CHLORO-9H-THIOXANTHEN-9-YLIDENE)PROPYL)-1-PIPERAZINYL)ETHYL ESTER
Common Name English
CIS-CLOPENTHIXOL DECANOATE
Common Name English
(Z)-CLOPENTHIXOL DECANOATE
Common Name English
ZUCLOPENTHIXOL DECANOATE [EP MONOGRAPH]
Common Name English
Zuclopenthixol decanoate [WHO-DD]
Common 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
CAS
64053-00-5
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
C95836
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
DTXSID201018303
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
DBSALT000787
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
58339
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
FDA UNII
TSS9KIZ5OG
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
SUB05196MIG
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
6450333
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
100000085821
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
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