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

Details

Stereochemistry ACHIRAL
Molecular Formula C19H22N2OS
Molecular Weight 326.456
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACEPROMAZINE

SMILES

CN(C)CCCN1C2=C(SC3=C1C=C(C=C3)C(C)=O)C=CC=C2

InChI

InChIKey=NOSIYYJFMPDDSA-UHFFFAOYSA-N
InChI=1S/C19H22N2OS/c1-14(22)15-9-10-19-17(13-15)21(12-6-11-20(2)3)16-7-4-5-8-18(16)23-19/h4-5,7-10,13H,6,11-12H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C19H22N2OS
Molecular Weight 326.456
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:15:27 UTC 2023
Edited
by admin
on Fri Dec 15 16:15:27 UTC 2023
Record UNII
54EJ303F0R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACEPROMAZINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
ATRAVET
Brand Name English
CONCENTRAT VO34
Brand Name English
ETHANONE, 1-(10-(3-(DIMETHYLAMINO)PROPYL)-10H-PHENOTHIAZIN-2-YL)-
Systematic Name English
ACEPROMAZINE [MI]
Common Name English
acepromazine [INN]
Common Name English
ACEPROMAZINE [MART.]
Common Name English
ACEZINE 2
Brand Name English
ACETYLPROMAZINE
Common Name English
10-(3-(DIMETHYLAMINO)PROPYL)PHENOTHIAZIN-2-YL METHYL KETONE
Systematic Name English
ACP
Common Name English
ACE
Common Name English
Acepromazine [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-VATC QN05AA04
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
WHO-ATC N05AA04
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
NCI_THESAURUS C66883
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
CFR 21 CFR 522.23
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL39560
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
DAILYMED
54EJ303F0R
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
RXCUI
155
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY RxNorm
NCI_THESAURUS
C77568
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
DRUG CENTRAL
73
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
FDA UNII
54EJ303F0R
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
CAS
61-00-7
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
CHEBI
44932
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
INN
667
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
MESH
D000075
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
MERCK INDEX
m1303
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID1022552
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
PUBCHEM
6077
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
SMS_ID
100000087916
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
DRUG BANK
DB01614
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-496-0
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
EVMPD
SUB05213MIG
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
WIKIPEDIA
ACEPROMAZINE
Created by admin on Fri Dec 15 16:15:28 UTC 2023 , Edited by admin on Fri Dec 15 16:15:28 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
TARGET -> INHIBITOR
IC50
TARGET -> INHIBITOR
TRANSPORTER -> SUBSTRATE
Increased sedation seen in dogs with the ABCB1-1Δ mutation.
Related Record Type Details
ACTIVE MOIETY