Drug intelligence / Profile preview

scopolamine + chlorpromazine

Development stage
Unknown
Modality
Small Molecules
Administration
Oral, Intravenous, Intramuscular, Subcutaneous, Transdermal, Rectal
01

Overview

Scopolamine + chlorpromazine is a combination of two pharmaceutical drugs, each with distinct mechanisms of action. Scopolamine is an anticholinergic agent that acts as a competitive antagonist at muscarinic acetylcholine receptors, primarily used to prevent nausea and vomiting associated with motion sickness and postoperative states. Chlorpromazine is a first-generation (typical) antipsychotic that functions mainly as an antagonist at dopamine D2 receptors in the brain, but also blocks other receptor types including histaminergic, adrenergic, and muscarinic receptors. It is used for the treatment of psychotic disorders such as schizophrenia and bipolar disorder, as well as for controlling severe nausea and vomiting, persistent hiccups, preoperative anxiety, porphyria, tetanus adjunct therapy, and behavioral disturbances in children[1][3][5][6][8]. The combination may be considered when both antiemetic (anti-nausea) effects are desired alongside management of psychiatric or neurological symptoms.

02

Targets

HRH1 (Histamine H1 Receptor)mAChR (Muscarinic acetylcholine receptors)DRD1 (Dopamine D1 Receptor)ADRA1A (α1A)DRD2 (Dopamine D2 Receptor)DRD3 (Dopamine receptor D3)

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