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Details

Stereochemistry ACHIRAL
Molecular Formula C21H23N3OS.CH4O3S
Molecular Weight 461.597
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Periciazine mesylate

SMILES

CS(O)(=O)=O.OC1CCN(CCCN2C3=CC=CC=C3SC4=CC=C(C=C24)C#N)CC1

InChI

InChIKey=QRWIJMNDSHDQJS-UHFFFAOYSA-N
InChI=1S/C21H23N3OS.CH4O3S/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;1-5(2,3)4/h1-2,4-7,14,17,25H,3,8-13H2;1H3,(H,2,3,4)

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

Molecular Formula CH4O3S
Molecular Weight 96.106
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
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
[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
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
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
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
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 Sat Dec 16 19:12:19 GMT 2023
Edited
by admin
on Sat Dec 16 19:12:19 GMT 2023
Record UNII
CC4X7ZP2DZ
Record Status Validated (UNII)
Record Version
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Name Type Language
Periciazine mesylate
Common Name English
Periciazine mesilate [WHO-DD]
Common Name English
Periciazine mesilate
Common Name English
10H-Phenothiazine-2-carbonitrile, 10-[3-(4-hydroxy-1-piperidinyl)propyl]-, methanesulfonate (1:1)
Systematic Name English
10H-Phenothiazine-2-carbonitrile, 10-[3-(4-hydroxy-1-piperidinyl)propyl]-, monomethanesulfonate
Systematic Name English
10-(3-(4-HYDROXY-1-PIPERIDINO) PROPYL)-10H-PHENOTHIAZINE-2-CARBONITRILE MONOMETHANESULFONATE
Systematic Name English
Code System Code Type Description
PUBCHEM
131888148
Created by admin on Sat Dec 16 19:12:20 GMT 2023 , Edited by admin on Sat Dec 16 19:12:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID60915707
Created by admin on Sat Dec 16 19:12:20 GMT 2023 , Edited by admin on Sat Dec 16 19:12:20 GMT 2023
PRIMARY
CAS
94291-99-3
Created by admin on Sat Dec 16 19:12:20 GMT 2023 , Edited by admin on Sat Dec 16 19:12:20 GMT 2023
PRIMARY
FDA UNII
CC4X7ZP2DZ
Created by admin on Sat Dec 16 19:12:20 GMT 2023 , Edited by admin on Sat Dec 16 19:12:20 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE