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

Details

Stereochemistry ACHIRAL
Molecular Formula C16H18N2S
Molecular Weight 270.393
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENETHAZINE

SMILES

CN(C)CCN1C2=C(SC3=C1C=CC=C3)C=CC=C2

InChI

InChIKey=PFAXACNYGZVKMX-UHFFFAOYSA-N
InChI=1S/C16H18N2S/c1-17(2)11-12-18-13-7-3-5-9-15(13)19-16-10-6-4-8-14(16)18/h3-10H,11-12H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C16H18N2S
Molecular Weight 270.393
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

FENETHAZINE was a first-generation phenothiazine-derived antihistamine drug. Promethazine was derived from FENETHAZINE.

Approval Year

PubMed

PubMed

TitleDatePubMed
The 50th Anniversary of Chlorpromazine.
2002-09
Substance Class Chemical
Created
by admin
on Wed Apr 02 09:33:26 GMT 2025
Edited
by admin
on Wed Apr 02 09:33:26 GMT 2025
Record UNII
8J97CUZ4HX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENETHAZINE [MI]
Preferred Name English
FENETHAZINE
INN   MI   WHO-DD  
INN  
Official Name English
Fenethazine [WHO-DD]
Common Name English
10-(2-DIMETHYLAMINOETHYL)PHENOTHIAZINE
Systematic Name English
fenethazine [INN]
Common Name English
PHENETHAZINE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29578
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
Code System Code Type Description
DRUG CENTRAL
3747
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
MESH
C014551
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
NCI_THESAURUS
C65646
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-325-1
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID30200233
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
ChEMBL
CHEMBL2106299
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
EVMPD
SUB07558MIG
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
INN
1860
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
CAS
522-24-7
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
FDA UNII
8J97CUZ4HX
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
PUBCHEM
68223
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
WIKIPEDIA
Fenethazine
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
MERCK INDEX
m186
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY Merck Index
SMS_ID
100000081252
Created by admin on Wed Apr 02 09:33:26 GMT 2025 , Edited by admin on Wed Apr 02 09:33:26 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
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ACTIVE MOIETY