U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C19H23ClN2S
Molecular Weight 346.917
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORPROETHAZINE

SMILES

CCN(CC)CCCN1C2=CC(Cl)=CC=C2SC3=C1C=CC=C3

InChI

InChIKey=DBOUGBAQLIXZLV-UHFFFAOYSA-N
InChI=1S/C19H23ClN2S/c1-3-21(4-2)12-7-13-22-16-8-5-6-9-18(16)23-19-11-10-15(20)14-17(19)22/h5-6,8-11,14H,3-4,7,12-13H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C19H23ClN2S
Molecular Weight 346.917
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Chlorproethazine (Neuriplege) is a neuroleptic, antipsychotic and muscle relaxant. Neuriplege® cream was available as a non‐prescription medication in France until its withdrawal from the market by regulatory authorities in January 2007. Neuriplege caused phototoxicity and photocontact allergy.

Approval Year

PubMed

PubMed

TitleDatePubMed
Contact sensitization to chlorproethazine can induce persistent light reaction and cross-photoreactions to other phenothiazines.
2001 Jun
Combined quinacrine and chlorpromazine therapy in fatal familial insomnia.
2004 Jul-Aug
Photocontact allergic and phototoxic studies of chlorproethazine.
2008 Feb
Toxic effects of chlorpromazine on Carassius auratus and its oxidative stress.
2008 Nov
Comparative effects of cationic triarylmethane, phenoxazine and phenothiazine dyes on horse serum butyrylcholinesterase.
2008 Oct 15
Hypothermia increases interleukin-6 and interleukin-10 in juvenile endotoxemic mice.
2010 Jan
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:52:21 GMT 2023
Edited
by admin
on Sat Dec 16 16:52:21 GMT 2023
Record UNII
960NX27Z07
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLORPROETHAZINE
INN   MI   WHO-DD  
INN  
Official Name English
chlorproethazine [INN]
Common Name English
Chlorproethazine [WHO-DD]
Common Name English
CHLORPROETHAZINE [MI]
Common Name English
2-CHLORO-10-(3-DIETHYLAMINOPROPYL)PHENOTHIAZINE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C66880
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
WHO-VATC QN05AA07
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
WHO-ATC N05AA07
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
Code System Code Type Description
INN
1147
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-510-8
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
SMS_ID
100000081893
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
DRUG CENTRAL
619
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
CAS
84-01-5
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
DRUG BANK
DB13382
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
WIKIPEDIA
CHLORPROETHAZINE
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
FDA UNII
960NX27Z07
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
NCI_THESAURUS
C79580
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
ChEMBL
CHEMBL52125
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
MESH
C054028
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
PUBCHEM
65750
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID80232882
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
MERCK INDEX
m3459
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY Merck Index
RXCUI
59860
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY RxNorm
EVMPD
SUB06206MIG
Created by admin on Sat Dec 16 16:52:21 GMT 2023 , Edited by admin on Sat Dec 16 16:52:21 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY