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Details

Stereochemistry ACHIRAL
Molecular Formula C21H23N3OS
Molecular Weight 365.492
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PERICIAZINE

SMILES

OC1CCN(CCCN2C3=CC(=CC=C3SC4=C2C=CC=C4)C#N)CC1

InChI

InChIKey=LUALIOATIOESLM-UHFFFAOYSA-N
InChI=1S/C21H23N3OS/c22-15-16-6-7-21-19(14-16)24(18-4-1-2-5-20(18)26-21)11-3-10-23-12-8-17(25)9-13-23/h1-2,4-7,14,17,25H,3,8-13H2

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including http://www.rlsnet.ru/mnn_index_id_1016.htm#primenenie--veshhestva-periciazin | https://www.ncbi.nlm.nih.gov/pubmed/7918347 | https://www.ncbi.nlm.nih.gov/pubmed/24825770

Periciazine (INN), also known as pericyazine (BAN) or Propericiazine, is a drug that belongs to the phenothiazine class of typical antipsychotics. Pericyazine is not approved for sale in the United States. It is commonly sold in Canada and Russia under the tradename Neuleptil and in the United Kingdom and Australia under the tradename Neulactil. The primary uses of pericyazine include the short-term treatment of severe anxiety or tension and in the maintenance treatment of psychotic disorders such as schizophrenia. There is insufficient evidence to determine whether periciazine is more or less effective than other antipsychotics. Pericyazine is a rather sedating and anticholinergic antipsychotic, and despite being classed with the typical antipsychotics, its risk of extrapyramidal side effects is comparatively low. It has a relatively high risk of causing hyperprolactinemia and a moderate risk of causing weight gain and orthostatic hypotension.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
10.0 nM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Neuleptil

Approved Use

Unknown
Primary
Neuleptil

Approved Use

Unknown
Primary
Neuleptil

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Use of pimozide in the Pisa syndrome.
1992 Aug
Spectrophotometric determination of cerium(IV) using a phenothiazine derivative.
2002 Feb
Dose-related effects of propericiazine in rats.
2003 Feb
Atypical properties of several classes of antipsychotic drugs on the basis of differential induction of Fos-like immunoreactivity in the rat brain.
2004 Nov 26
Interactions between antiepileptic and antipsychotic drugs.
2006
Relationship between obesity and antipsychotic drug use in the adult population: a longitudinal, retrospective claim database study in Primary Care settings.
2008 Feb
Mechanism of interaction between human serum albumin and N-alkyl phenothiazines studied using spectroscopic methods.
2008 Jun 9
Symptoms and sleep patterns during inpatient treatment of methamphetamine withdrawal: a comparison of mirtazapine and modafinil with treatment as usual.
2008 Oct
Antipsychotics and risk of venous thromboembolism: A population-based case-control study.
2009 Aug 9
Neuroleptic malignant syndrome or a statin drug reaction? A case report.
2009 Nov-Dec
All is not lost: utilizing continuous remote ILR monitoring to diagnose syncope.
2010 Jun 1
Patents

Patents

Sample Use Guides

50 mg/day for two days, thereafter a flexible dosage schedule was followed until therapeutic effect achieved.
Route of Administration: Oral
In Vitro Use Guide
One hundred microlitres of [3H]SCH23390 (1 nM, 90 Ci/mmol), competing drug solution (100 mkl of variable concentrations) and 50 mM Tris-HCl buffer (700 gl) containing no NaCl or KCI were placed in glass tubes. The solutions were stirred using a vortex mixer. One hundred microlitres of membrane preparation (2.5 mg wet tissue/tube) were added and the solution was again stirred using a vortex mixer. Solutions were incubated for 30 min at 37 C. Incubations were terminated by rapid filtration under vacuum using Whatman GF/B filters (24 mm diameter). The tubes and filters were rinsed with 6 ml ice-cold saline. The filters were punched out and placed in a 20 ml glass vial with 10 ml scintillation cocktail. After the samples stood six hours, radioactivities were measured using a Beckman LS 7800 liquid scintillation counter. The specific bound was defined as the total amount of [3H]SCH23390 bound (zero unlabelled ligands) minus the nonspecific amount bound (binding in presence of 1mkM SCH23390).
Name Type Language
PERICIAZINE
INN   WHO-DD  
INN  
Official Name English
RP 8909SKF 20716
Code English
PERICYAZINE [MI]
Common Name English
SKF-20716
Code English
PROPERICIAZINE
JAN  
Common Name English
RP 8909
Code English
Periciazine [WHO-DD]
Common Name English
NSC-758641
Code English
PERICYAZINE [MART.]
Common Name English
periciazine [INN]
Common Name English
SKF 20716
Code English
10-(3-(4-HYDROXYPIPERIDINO)PROPYL)PHENOTHIAZINE-2-CARBONITRILE
Systematic Name English
PROPERICIAZINE [JAN]
Common Name English
RP-8909
Code English
PERICYAZINE
MART.   MI  
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29710
Created by admin on Fri Dec 15 15:14:06 GMT 2023 , Edited by admin on Fri Dec 15 15:14:06 GMT 2023
WHO-ATC N05AC01
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WHO-VATC QN05AC01
Created by admin on Fri Dec 15 15:14:06 GMT 2023 , Edited by admin on Fri Dec 15 15:14:06 GMT 2023
Code System Code Type Description
CAS
2622-26-6
Created by admin on Fri Dec 15 15:14:06 GMT 2023 , Edited by admin on Fri Dec 15 15:14:06 GMT 2023
PRIMARY
ECHA (EC/EINECS)
220-071-3
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PRIMARY
EPA CompTox
DTXSID5045910
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PRIMARY
RXCUI
8766
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PRIMARY RxNorm
MESH
C084584
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PRIMARY
SMS_ID
100000082753
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PRIMARY
EVMPD
SUB09727MIG
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PRIMARY
PUBCHEM
4747
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PRIMARY
ChEMBL
CHEMBL251940
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PRIMARY
MERCK INDEX
m8549
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PRIMARY Merck Index
NCI_THESAURUS
C81580
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PRIMARY
INN
1398
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DRUG CENTRAL
2107
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PRIMARY
DRUG BANK
DB01608
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WIKIPEDIA
PERICYAZINE
Created by admin on Fri Dec 15 15:14:06 GMT 2023 , Edited by admin on Fri Dec 15 15:14:06 GMT 2023
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FDA UNII
3405M6FD73
Created by admin on Fri Dec 15 15:14:06 GMT 2023 , Edited by admin on Fri Dec 15 15:14:06 GMT 2023
PRIMARY
NSC
758641
Created by admin on Fri Dec 15 15:14:06 GMT 2023 , Edited by admin on Fri Dec 15 15:14:06 GMT 2023
PRIMARY
CHEBI
31981
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PRIMARY