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

Details

Stereochemistry RACEMIC
Molecular Formula C20H26N2S
Molecular Weight 326.499
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETYMEMAZINE

SMILES

CCC1=CC=C2SC3=CC=CC=C3N(CC(C)CN(C)C)C2=C1

InChI

InChIKey=USKHCLAXJXCWMO-UHFFFAOYSA-N
InChI=1S/C20H26N2S/c1-5-16-10-11-20-18(12-16)22(14-15(2)13-21(3)4)17-8-6-7-9-19(17)23-20/h6-12,15H,5,13-14H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C20H26N2S
Molecular Weight 326.499
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

PubMed

PubMed

TitleDatePubMed
[DEMENTIA PRAECOX. CURE BY RP-6484].
1963-12
[On the clinical use in neuropsychiatry of 3-ethyl-10-(2-methyl-3-dimethylaminopropyl)-phenothiazine HCl (RP-6484), new phenothiazine neuroleptic].
1962-06-02
[Clinical study of a new phenothiazine derivative, RP-6484].
1960-06-11

Sample Use Guides

Pigs: Ethyl isobutrazine (Etymemazine) and pethidine were each administered at a dose rate of 5 mg/kg
Route of Administration: Intramuscular
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:19:33 GMT 2025
Edited
by admin
on Mon Mar 31 19:19:33 GMT 2025
Record UNII
861J4K81C7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHOTRIMEPRAZINE
Preferred Name English
ETYMEMAZINE
INN   MI  
INN  
Official Name English
ETHYLISOBUTRAZINE
Common Name English
etymemazine [INN]
Common Name English
ETYMEMAZINE [MI]
Common Name English
10-(3-(DIMETHYLAMINO)-2-METHYLPROPYL)-2-ETHYLPHENOTHIAZINE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
CFR 21 CFR 520.863
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
NCI_THESAURUS C29578
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
CFR 21 CFR 522.863
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
Code System Code Type Description
FDA UNII
861J4K81C7
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
DRUG CENTRAL
3742
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
SMS_ID
100000082117
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
EVMPD
SUB07349MIG
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
INN
1391
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
CAS
523-54-6
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
ChEMBL
CHEMBL2008544
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
DRUG BANK
DB11517
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
PUBCHEM
71823
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
NCI_THESAURUS
C73062
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
EPA CompTox
DTXSID0046935
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
MERCK INDEX
m728
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY Merck Index
WIKIPEDIA
ETYMEMAZINE
Created by admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY