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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

Molecular Formula C21H23N3OS
Molecular Weight 365.492
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Successful treatment of low-flow priapism associated with phenothiazine therapy.
2001 Sep
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
Cloud point extraction and preconcentration for the gas chromatography of phenothiazine tranquilizers in spiked human serum.
2004 Sep
[Methodological bases of early psychosocial rehabilitation of poststroke patients in neurological hospital].
2005
[Wilson's disease: clinical diagnosis and "faces of panda" signs in magnetic resonance imaging. Case report].
2005 Mar
Analysis of phenothiazines in human body fluids using disk solid-phase extraction and liquid chromatography.
2005 Nov-Dec
Interactions between antiepileptic and antipsychotic drugs.
2006
Antipsychotics-induced hypersensitivity of visual perception.
2006 Jul
Antipsychotic medication dispensing and associated odds ratios of death in elderly veterans and war widows, 2001.
2006 Nov-Dec
QT interval and dispersion in very young children treated with antipsychotic drugs: a retrospective chart review.
2007 Apr
Simple and simultaneous determination for 12 phenothiazines in human serum by reversed-phase high-performance liquid chromatography.
2007 Jul 1
Discovery of antiandrogen activity of nonsteroidal scaffolds of marketed drugs.
2007 Jul 17
The effect of antipsychotic medication on sexual function and serum prolactin levels in community-treated schizophrenic patients: results from the Schizophrenia Trial of Aripiprazole (STAR) study (NCT00237913).
2008 Dec 22
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
[Treatment of a serious autistic disorder in a child with Naltrexone in an oral suspension form].
2009 Apr
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).
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:14:06 GMT 2023
Edited
by admin
on Fri Dec 15 15:14:06 GMT 2023
Record UNII
3405M6FD73
Record Status Validated (UNII)
Record Version
  • Download
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
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-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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PRIMARY
DRUG CENTRAL
2107
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PRIMARY
DRUG BANK
DB01608
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
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
PRIMARY
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
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
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