Haloperidol decanoate
CAT:
804-HY-107969-01
Size:
5 mg
For Laboratory Research Only. Not for Clinical or Personal Use.
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- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


Haloperidol decanoate
Description:
Haloperidol decanoate is a depot preparation of haloperidol, a commonly used butyrophenone derivative with antipsychotic activity. Haloperidol decanoate can increase the striatal D2 receptor in rat. Haloperidol decanoate can improve conditions of psychoses (mainly schizophrenia) . Haloperidol decanoate can lead to increased accumulation of the dopamine metabolites homo-vanillic acid. Haloperidol decanoate can reduce intestinal transport, increase gastric emptying and reduce acid output in rat model[1][4].UNSPSC:
12352005Hazard Statement:
H302, H413Target:
COX; Dopamine Receptor; NO SynthaseType:
Reference compoundRelated Pathways:
GPCR/G Protein; Immunology/Inflammation; Neuronal SignalingApplications:
Neuroscience-NeuromodulationField of Research:
Neurological Disease; CancerAssay Protocol:
https://www.medchemexpress.com/haloperidol-decanoate.htmlPurity:
99.67Solubility:
DMSO : 100 mg/mL (ultrasonic)Smiles:
CCCCCCCCCC (OC1 (C2=CC=C (Cl) C=C2) CCN (CCCC (C3=CC=C (F) C=C3) =O) CC1) =OMolecular Formula:
C31H41ClFNO3Molecular Weight:
530.11Precautions:
H302, H413References & Citations:
[1]R Beresford, et al. Haloperidol decanoate. A preliminary review of its pharmacodynamic and pharmacokinetic properties and therapeutic use in psychosis. Drugs. 1987 Jan;33 (1) :31-49.|[2]Schmitz, I., et al., (2025) . A single dose of haloperidol decanoate induces short-term hippocampal neuroinflammation: focus on the glial response. Pharmacological reports : PR, 77 (3), 800–808. |[3]Oh-e, Y., et al., (1991) . Pharmacokinetics of haloperidol decanoate in rats. Journal of pharmacobio-dynamics, 14 (11), 615–622.|[4]Akiyama, K., et al., (1987) . Effect of chronic administration of haloperidol (intermittently) and haloperidol-decanoate (continuously) on D2 dopamine and muscarinic cholinergic receptors and on carbachol-stimulated phosphoinositide hydrolysis in the rat striatum. The Japanese journal of psychiatry and neurology, 41 (2), 311–320.Shipping Conditions:
Blue IceStorage Conditions:
-20°C, 3 years (Powder)Scientific Category:
Reference compound1Clinical Information:
LaunchedCAS Number:
74050-97-8
