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Pimozide

Catalog No.
C3837
dopamine receptors inhibitor
Grouped product items
SizePriceStock Qty
100mg
$62.00
In stock
250mg
$138.00
Ship with 5-10 days

Tel: +1-832-696-8203

Email: [email protected]

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Background

Pimozide is a chemically novel, highly potent and orally long-acting neuroleptic dopamine receptors inhibitor [1].

Dopamine receptors belong to G protein-coupled receptor containing five subtypes termed D1, D2, D3, D4, and D5. Dopamine receptors have been involved in many physiological functions of the catecholaminergic neurotransmitter dopamine, ranging from voluntary movement to hormonal regulation and hypertension. Pharmacological drugs targeting dopaminergic neurotransmission have been clinically used in several neurological and psychiatric disorders, such as schizophrenia, Parkinson's disease, Huntington's disease, bipolar disorder, attention deficit hyperactivity disorder (ADHD), and Tourette's syndrome [2].

In vitro: Pimozide displayed high affinity for dopamine receptors. The Ki values for D2, D3, and D4 were 2.4, 0.2, and 1.8 nM, respectively [3].

In vivo: In hungry rats, pimozide attenuated lever-pressing and running for food reward. Pimozide pretreatment attenuated acquisition of a lever-pressing habit motivated by food reward in a dose-dependent manner[4]. In 31 male Wistar rats self-administering cocaine, pimozide caused a dose-dependent (0.0625–0.5 mg/kg) acceleration of responding [5].

Clinical trials: Pimozide was effective in treating Tourette's syndrome and positive psychotic symptoms in schizophrenia. Results from studies ranging from clinical vignettes to controlled trials indicated that pimozide also ameliorated negative schizophrenic symptoms, treated monosymptomatic delusional psychosis resistant to other neuroleptics, and treated pain syndromes [6].

References:
[1] Janssen P A, Niemegeers C J, Schellekens K H, et al.  Pimozide, a chemically novel, highly potent and orally long-acting neuroleptic drug. I. The comparative pharmacology of pimozide, haloperidol, and chlorpromazine[J]. Arzneimittel-Forschung, 1968, 18(3): 261-279.
[2] Beaulieu J M, Gainetdinov R R.  The physiology, signaling, and pharmacology of dopamine receptors[J]. Pharmacological reviews, 2011, 63(1): 182-217.
[3] Burstein E S, Ma J, Wong S, et al.  Intrinsic efficacy of antipsychotics at human D2, D3, and D4 dopamine receptors: identification of the clozapine metabolite N-desmethylclozapine as a D2/D3 partial agonist[J]. Journal of Pharmacology and Experimental Therapeutics, 2005, 315(3): 1278-1287.
[4] Wise R A, Schwartz H V.  Pimozide attenuates acquisition of lever-pressing for food in rats[J]. Pharmacology Biochemistry and Behavior, 1981, 15(4): 655-656.
[5] De Wit H, Wise R A.  Blockade of cocaine reinforcement in rats with the dopamine receptor blocker pimozide, but not with the noradrenergic blockers phentolamine or phenoxybenzamine[J]. Canadian Journal of Psychology/Revue canadienne de psychologie, 1977, 31(4): 195.
[6] Opler L A, Feinberg S S.  The role of pimozide in clinical psychiatry: a review[J]. Journal of Clinical Psychiatry, 1991.

Chemical Properties

StorageStore at -20°C
M.Wt461.6
Cas No.2062-78-4
FormulaC28H29F2N3O
SynonymsNSC 170984,Orap,R 6238
Solubilityinsoluble in H2O; insoluble in EtOH; ≥17.95 mg/mL in DMSO
Chemical Name1-[1-[4,4-bis(4-fluorophenyl)butyl]-4-piperidinyl]-1,3-dihydro-2H-benzimidazol-2-one
SDFDownload SDF
Canonical SMILESFC1=CC=C(C(CCCN2CCC(N3C(NC4=C3C=CC=C4)=O)CC2)C5=CC=C(F)C=C5)C=C1
Shipping ConditionShip with blue ice, or upon other requests.
General tipsFor obtaining a higher solubility, please warm the tube at 37°C and shake it in the ultrasonic bath for a while.

Quality Control

Quality Control & MSDS

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Chemical structure

Pimozide