Drug intelligence / Profile preview

zuclopenthixol decanoate

Development stage
Unknown
Lead developer
The Centaur Company
Modality
Small Molecules
Administration
Intramuscular
01

Overview

Zunorma Max (zuclopenthixol decanoate) is a long-acting depot formulation of the typical antipsychotic zuclopenthixol, originally developed by Lundbeck and marketed by The Centaur Company. It is indicated for the maintenance treatment of schizophrenia, chronic psychoses, and acute manic episodes. As a thioxanthene derivative, zuclopenthixol decanoate acts primarily as an antagonist at dopamine D1 and D2 receptors in the brain, thereby reducing excessive dopaminergic transmission associated with psychotic symptoms. It also exhibits high affinity for alpha-1 adrenergic and 5-HT2 receptors. Administered as a deep intramuscular injection, the decanoate ester is slowly released from the muscle depot and hydrolyzed into active zuclopenthixol, providing sustained therapeutic levels over several weeks.

Brand names
Zunorma Max
Other names
cis(Z)-clopenthixol decanoatecis-clopenthixol decanoatezuclopenthixol decanoatezuclopentixol decanoate
02

Targets

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

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