CHEBI:44932 - acepromazine

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ChEBI Name acepromazine
ChEBI ID CHEBI:44932
Definition A member of the class of phenothiazines that is 10H-phenothiazine substituted by an acetyl group at position 2 and a 3-(dimethylamino)propyl group at position 10.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:37967, CHEBI:44928
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Formula C19H22N2OS
Net Charge 0
Average Mass 326.45686
Monoisotopic Mass 326.145
InChI 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
InChIKey NOSIYYJFMPDDSA-UHFFFAOYSA-N
SMILES CN(C)CCCN1c2ccccc2Sc2ccc(cc12)C(C)=O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Application(s): phenothiazine antipsychotic drug

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ChEBI Ontology
Outgoing acepromazine (CHEBI:44932) has role phenothiazine antipsychotic drug (CHEBI:37930)
acepromazine (CHEBI:44932) is a aromatic ketone (CHEBI:76224)
acepromazine (CHEBI:44932) is a methyl ketone (CHEBI:51867)
acepromazine (CHEBI:44932) is a phenothiazines (CHEBI:38093)
acepromazine (CHEBI:44932) is a tertiary amino compound (CHEBI:50996)
IUPAC Name
1-{10-[3-(dimethylamino)propyl]-10H-phenothiazin-2-yl}ethanone
Synonyms Sources
1-[10-(3-DIMETHYLAMINO-PROPYL)-10H-PHENOTHIAZIN-2-YL]-ETHANONE PDBeChem
10-(3-dimethylaminopropyl)phenothiazin-3-yl methyl ketone ChemIDplus
10-(3-dimethylaminopropyl)phenothiazine-3-ethylone ChemIDplus
acepromazine NIST Chemistry WebBook
acetazine NIST Chemistry WebBook
acetopromazine ChemIDplus
acetylpromazine ChemIDplus
Manual Xrefs Databases
73 DrugCentral
Acepromazine Wikipedia
D07065 KEGG DRUG
DB01614 DrugBank
HMDB0015552 HMDB
LSM-4609 LINCS
PMZ PDBeChem
US4213981 Patent
View more database links
Registry Numbers Types Sources
40187 Beilstein Registry Number Beilstein
40187 Reaxys Registry Number Reaxys
61-00-7 CAS Registry Number ChemIDplus
61-00-7 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
23627379 PubMed citation Europe PMC
23642485 PubMed citation Europe PMC
24171559 PubMed citation Europe PMC
24575797 PubMed citation Europe PMC
Last Modified
22 February 2017