CHEBI:4657 - disopyramide

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ChEBI Name disopyramide
ChEBI ID CHEBI:4657
Definition A monocarboxylic acid amide that is butanamide substituted by a diisopropylamino group at position 4, a phenyl group at position 2 and a pyridin-2-yl group at position 2. It is used as a anti-arrhythmia drug.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C21H29N3O
Net Charge 0
Average Mass 339.47458
Monoisotopic Mass 339.231
InChI InChI=1S/C21H29N3O/c1-16(2)24(17(3)4)15-13-21(20(22)25,18-10-6-5-7-11-18)19-12-8-9-14-23-19/h5-12,14,16-17H,13,15H2,1-4H3,(H2,22,25)
InChIKey UVTNFZQICZKOEM-UHFFFAOYSA-N
SMILES CC(C)N(CCC(C(N)=O)(c1ccccc1)c1ccccn1)C(C)C
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): anti-arrhythmia drug
A drug used for the treatment or prevention of cardiac arrhythmias. Anti-arrhythmia drugs may affect the polarisation-repolarisation phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibres.
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ChEBI Ontology
Outgoing disopyramide (CHEBI:4657) has role anti-arrhythmia drug (CHEBI:38070)
disopyramide (CHEBI:4657) is a monocarboxylic acid amide (CHEBI:29347)
disopyramide (CHEBI:4657) is a pyridines (CHEBI:26421)
disopyramide (CHEBI:4657) is a tertiary amino compound (CHEBI:50996)
Incoming disopyramide phosphate (CHEBI:4658) has functional parent disopyramide (CHEBI:4657)
IUPAC Name
4-(diisopropylamino)-2-phenyl-2-pyridin-2-ylbutanamide
INNs Sources
disopiramida ChemIDplus
disopyramide ChemIDplus
disopyramidum ChemIDplus
Synonyms Sources
alpha-(2-(Diisopropylamino)ethyl)-alpha-phenyl-2-pyridineacetamide ChemIDplus
gamma-Diisopropylamino-alpha-phenyl-alpha-(2-pyridyl)butyramide ChemIDplus
Manual Xrefs Databases
926 DrugCentral
BE617730 Patent
C06965 KEGG COMPOUND
D00303 KEGG DRUG
DB00280 DrugBank
Disopyramide Wikipedia
LSM-1439 LINCS
US3225054 Patent
View more database links
Registry Numbers Types Sources
3737-09-5 CAS Registry Number ChemIDplus
492056 Beilstein Registry Number Beilstein
492056 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
16842817 PubMed citation Europe PMC
24502246 PubMed citation Europe PMC
Last Modified
22 February 2017