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

Details

Stereochemistry RACEMIC
Molecular Formula C19H25N3S
Molecular Weight 327.487
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMINOPROMAZINE

SMILES

CN(C)CC(CN1C2=CC=CC=C2SC3=CC=CC=C13)N(C)C

InChI

InChIKey=YZQNFFLGIYEXMM-UHFFFAOYSA-N
InChI=1S/C19H25N3S/c1-20(2)13-15(21(3)4)14-22-16-9-5-7-11-18(16)23-19-12-8-6-10-17(19)22/h5-12,15H,13-14H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C19H25N3S
Molecular Weight 327.487
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:31:47 GMT 2025
Edited
by admin
on Mon Mar 31 18:31:47 GMT 2025
Record UNII
S9SDD93U5U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMINOPROMAZINE
INN   MI  
INN  
Official Name English
AMINOPROMAZINE [MI]
Preferred Name English
aminopromazine [INN]
Common Name English
10-(2,3-BIS(DIMETHYLAMINO)PROPYL)PHENOTHIAZINE
Systematic Name English
AMINOPROPAZINE
Common Name English
PROQUAMEZINE
Common Name English
TETRAMEPROZINE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 520.82B
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
NCI_THESAURUS C29698
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
CFR 21 CFR 520.82
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
CFR 21 CFR 520.82A
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID00861592
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
INN
704
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
CAS
58-37-7
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
NCI_THESAURUS
C76457
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105961
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
EVMPD
SUB05445MIG
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
PUBCHEM
19392
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
DRUG BANK
DB15596
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
MERCK INDEX
m1733
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY Merck Index
RXCUI
2462496
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
FDA UNII
S9SDD93U5U
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
ECHA (EC/EINECS)
200-378-9
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
DAILYMED
S9SDD93U5U
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
SMS_ID
100000087208
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
DRUG CENTRAL
173
Created by admin on Mon Mar 31 18:31:47 GMT 2025 , Edited by admin on Mon Mar 31 18:31:47 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY