2062-78-4 Usage
Pharmacological action
In terms of pharmacological action, pimozide is similar to haloperidol. It is used in hospitals as well as in outpatient settings for supportive therapy of patients suffering from schizophrenia, paranoid conditions, and mental and neurotic disorders with paranoid characteristics. It is unfit for use in severe psychoses because it does not possess psychomotor-sedative action. It is used for treating patients who suffer from Turretts’s syndrome.
Description
Pimozide is a dopamine receptor antagonist (Kis = 2.4, 0.3, and 1.8 nM for D2, D3, and D4 receptors, respectively). It also binds to eight additional receptors (Kds = 25-3,100 nM for the human receptors) and inhibits the voltage-gated sodium channel Nav1.2 and the voltage-gated potassium channel Kv11.1 (IC50s = 42 and 340 nM, respectively). Pimozide (0.5, 1, and 2 mg/kg) decreases the number of licks and reduces fluid intake of a sweetened solution in rats. It decreases the number of threats and attacks and increases immobility time in the neutral arena aggression test, indicating increased passiveness, in male mice when administered at a dose of 0.75 mg/kg for 10 days. Formulations containing pimozide have been used in the treatment of Tourette syndrome.
Chemical Properties
White or almost white powder.
Originator
Orap ,Janssen, W. Germany ,1971
Uses
Different sources of media describe the Uses of 2062-78-4 differently. You can refer to the following data:
1. Pimozide is a D2 dopamine receptor antagonist that binds to the cloned 5-HT7 receptor with high affinity (1,2,3,4). Pimozide is also a Ca2+ channel antagonist. Pimozide is used as an antipsychotic.
2. Used for the suppression of motor and phonic tics in patients with Tourette's Disorder who have failed to respond satisfactorily to standard treatment.
Definition
ChEBI: Pimozide is a member of the class of benzimidazoles that is 1,3-dihydro-2H-benzimidazol-2-one in which one of the nitrogens is substituted by a piperidin-4-yl group, which in turn is substituted on the nitrogen by a 4,4-bis(p-fluorophenyl)butyl group. It has a role as a H1-receptor antagonist, a serotonergic antagonist, a first generation antipsychotic, an antidyskinesia agent and a dopaminergic antagonist. It is a member of benzimidazoles, an organofluorine compound and a heteroarylpiperidine.
Brand name
Orap (Teva).
General Description
Pimozide, 1-[1-[4,4-bis(p-fluorophenyl)butyl]-4-piperidyl]-2-benzimidazolinone (Orap), isa white to creamy white solid (pKa＝9.42). Pimozide is 50%absorbed after oral administration. It is metabolized byCYP450 enzymes, in particular the CYP3A4 and CYP1A2isozymes, to inactive metabolites. Pimozide is excreted in theurine and to a lesser extent in the feces. Toxic effects may beproduced with pimozide in the presence of inducers or inhibitorsof CYP3A4 and CYP1A2. Pimozide is also a stronginhibitor of CYP2D6 without appearing to be an importantsubstrate of this isoform.99 The use of pimozide in the UnitedStates is small, but it is a critical drug for many patients withGilles de la Tourette disorder who cannot tolerate haloperidol.
Biological Activity
Dopamine D 2 -receptor antagonist and antipsychotic which binds with very high affinity to the cloned rat 5-HT 7 receptor (K i = 0.5 nM).
Biochem/physiol Actions
D2 dopamine receptor antagonist; binds with high affinity to the cloned 5-HT7 receptor; Ca2+ channel antagonist; antipsychotic
Pharmacology
Pimozide is an orally active antipsychotic drug product which shares with other antipsychotics the ability to blockade dopaminergic receptors on neurons in the central nervous system. However, receptor blockade is often accompanied by a series of secondary alterations in central dopamine metabolism and function which may contribute to both pimozide's therapeutic and untoward effects. In addition, pimozide, in common with other antipsychotic drugs, has various effects on other central nervous system receptor systems which are not fully characterized. Pimozide also has less potential for inducing sedation and hypotension as it has more specific dopamine receptor blocking activity than other neuroleptic agents (and is therefore a suitable alternative to haloperidol).
Synthesis
Pimozide, 1-[1-[4,4-bis-(p-fluorophenyl)butyl]-4-piperidyl]-2-benzymidazolinone (6.6.5), is structurally very similar to droperidol with the exception of the presence of a double bond in the piperidine ring and the substitution of a p-fluorobutyrophenone group on the nitrogen atom of the piperidine ring with a 4,4-bis-(p-fluorophenyl)-butyl radical. 4,4-bis-(p-fluorophenyl)-butylchloride (bromide) (6.6.3), which is needed for the synthesis of pimozide as well as fluspirylene and penfluridol, is synthesized by reacting of two moles of 4-p-fluorophenylmagnesiumbromide with cyclopropancarboxylic acid ester, which results in the formation of bis-(4-p-fluorophenyl)cyclopropylcarbinol (6.6.1). Treatment of this with thionyl chloride (phosphorous tribromide) leads to opening of the cyclopropyl ring, forming 1,1-bis-(4-fluorophenyl)-4-chloro(bromo)-1- butene (6.6.2). Reduction of the double bond using hydrogen over a palladium catalyst leads to the formation of 1,1-bis-(4-fluoro- phenyl)butyl chloride (bromide) (6.6.3) [60–63].
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].
Drug interactions
Potentially hazardous interactions with other drugs
Anaesthetics: enhanced hypotensive effect.
Analgesics: increased risk of convulsions with
tramadol; enhanced hypotensive and sedative
effects with opioids; increased risk of ventricular
arrhythmias with methadone.
Anti-arrhythmics: increased risk of ventricular
arrhythmias with anti-arrhythmics that prolong
the QT interval - avoid with amiodarone and
disopyramide (risk of ventricular arrhythmias). Antibacterials: avoid with macrolides and moxifloxacin
(increased risk of ventricular arrhythmias).
Antidepressants: concentration increased by SSRIs
- avoid; increased risk of ventricular arrhythmias
with SSRIs and tricyclics - avoid; increased risk of
ventricular arrhythmias with delamanid.
Antiepileptics: antagonises anticonvulsant effect.
Antifungals: avoid with imidazoles and triazoles -
risk of ventricular arrhythmias.
Antimalarials: avoid with artemether/lumefantrine and
piperaquine with artenimol; increased risk of ventricular
arrhythmias with mefloquine and quinine - avoid.
Antipsychotics: increased risk of ventricular
arrhythmias with droperidol, phenothiazines,
risperidone or sulpiride - avoid; concentration
possibly increased by lurasidone.
Antivirals: concentration increased by atazanavir,
boceprevir, efavirenz, fosamprenavir, indinavir,
ritonavir, saquinavir and telaprevir, increased risk of
ventricular arrhythmias - avoid.
Anxiolytics and hypnotics: increased sedative effects.
Aprepitant: avoid concomitant use.
Atomoxetine: increased risk of ventricular arrhythmias.
Beta-blockers: increased risk of ventricular
arrhythmias with sotalol.
Cobicistat: concentration possibly increased by
cobicistat - avoid.
Cytotoxics: use crizotinib with caution; avoid with
lapatinib and idelalisib; increased risk of ventricular
arrhythmias with panobinostat and vandetanib -
avoid; increased risk of ventricular arrhythmias with
arsenic trioxide.
Diuretics: increased risk of ventricular arrhythmias
due to hypokalaemia.
Fosaprepitant: avoid concomitant use.
Grapefruit juice: avoid concomitant use.
Ivabradine: increased risk of ventricular arrhythmias.
Metabolism
Pimozide is metabolised in the liver via the cytochrome P450
isoenzyme CYP3A4 and to a lesser extent by CYP2D6
mainly by N-dealkylation and excreted in the urine and
faeces in the form of metabolites and unchanged drug.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 2062-78-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2062-78:
(6*2)+(5*0)+(4*6)+(3*2)+(2*7)+(1*8)=64
64 % 10 = 4
So 2062-78-4 is a valid CAS Registry Number.
InChI:InChI=1/C28H29F2N3O/c29-22-11-7-20(8-12-22)25(21-9-13-23(30)14-10-21)4-3-17-32-18-15-24(16-19-32)33-27-6-2-1-5-26(27)31-28(33)34/h1-2,5-14,24-25H,3-4,15-19H2,(H,31,34)
2062-78-4Relevant articles and documents
Remote C(sp3)?H Arylation and Vinylation of N-Alkoxypyridinium Salts to δ-Aryl and δ-Vinyl Alcohols
Bao, Xu,Wang, Qian,Zhu, Jieping
, (2019/08/21)
The reaction of readily available and bench-stable N-alkoxypyridinium salts with arylboronic and vinylboronic acids afforded δ-aryl and δ-vinyl alcohols, respectively, in the presence of fac-Ir(ppy)3 and Cu(OTf)2 dual catalysts. The reaction takes place through a domino process involving the reductive generation of alkoxyl radicals, 1,5-hydrogen atom transfer (1,5-HAT) and the copper-catalyzed cross-coupling reaction of the resulting translocated carbon radicals with boronic acids. Complementary to the Minisci reaction, this method allows for the arylation of nucleophilic alkyl radicals with both electron-rich and electron-poor arenes under mild reaction conditions.
PREPARATION OF PHARMACEUTICAL ACTIVE INGREDIENTS USING A GLYCEROL-DERIVED SOLVENT
-
Page/Page column 10-11, (2008/12/07)
A process for the preparation of pharmaceutically active ingredients is provided, wherein the reaction is carried out in glycerol formal as inert solvent. In particular, the reaction is a nucleophilic substitution. Examples of active ingredients for which this process is particularly advantageous are loperamide and pimozide. The process of the present invention allows obtaining pharmaceutically active ingredients in highly safe and non-contaminant conditions, and with fewer energetic requirements.
