Drug intelligence / Profile preview

zuclopenthixole

Development stage
Unknown
Lead developer
Lundbeck
Modality
Small Molecules
Administration
Intramuscular
01

Overview

Zuclopenthixole is a first-generation (typical) antipsychotic of the thioxanthene class used primarily for the treatment of schizophrenia and other psychoses. It is available in several formulations including oral tablets (zuclopenthixole dihydrochloride), short-acting intramuscular injection (zuclopenthixole acetate), and long-acting depot injection (zuclopenthixole decanoate). The drug acts mainly as an antagonist at dopamine D1 and D2 receptors but also has high affinity for alpha1-adrenergic and 5-HT2 serotonin receptors. It has weaker activity at histamine H1 receptors and even lower affinity for muscarinic cholinergic and alpha2-adrenergic receptors. Zuclopenthixole is used to manage positive symptoms of schizophrenia such as hallucinations and delusions; it may also be used in acute mania associated with bipolar disorder or to control agitation in psychotic patients[2][4][5][6]. The drug was developed by Lundbeck Pharmaceuticals[6].

Brand names
ClopixolClopixol AcuphaseClopixol ConcentrateClopixol DepotCisordinolCisordinol DepotCisordinol-Acutard
Other names
zuclopenthixole dihydrochloridezuclopenthixole acetatezuclopenthixole decanoate
02

Targets

HRH1 (Histamine H1 Receptor)HTR2A (Serotonin receptor 5-HT2A)DRD1 (Dopamine D1 Receptor)ADRA1A (α1A)DRD2 (Dopamine D2 Receptor)

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