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QuickView for Encainide (compound)


PubChem
Name: Encainide
PubChem Compound ID: 48033
Description: One of the ANTI-ARRHYTHMIA AGENTS, it blocks SODIUM CHANNELS and slows conduction within the His-Purkinje system and myocardium.
Molecular formula: C22H28N2O2
Molecular weight: 352.47 g/mol
Synonyms:
BENZAMIDE, 4-METHOXY-N-(2-(2-(1-METHYL-2-PIPERIDINYL)ETHYL)PHENYL)-, (+-)-; BRN 0497572; Encainide; Encainidum [Latin]; 66778-36-7; Enkaid; Encainida [Spanish]; (+-)-4-Methoxy-N-(2-(2-(1-methyl-2-piperidinyl)ethyl)phenyl)benzamide; 5-22-09-00511 (Beilstein Handbook Reference); Encainide [French].
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DrugBank
Identification
Name: Encainide
Name (isomeric): DB01228
Drug Type: small molecule
Description: One of the ANTI-ARRHYTHMIA AGENTS, it blocks SODIUM CHANNELS and slows conduction within the His-Purkinje system and myocardium.
Synonyms:
Encainidum [Latin]; Encainida [Spanish]; Encainide [French]
Brand: Enkaid
Category: Antiarrhythmic Agents, Sodium channel blockers, Anti-Arrhythmia Agents
CAS number: 66778-36-7
Pharmacology
Indication: Encainide is a class Ic antiarrhythmic agent which was used for management of irregular heartbeats, such as atrial fibrillation, atrial flutter, ventricular tachycardia, and ventricular fibrillation.
Pharmacology:
Used to treat irregular heartbeats, encainide decreases excitability, conduction velocity, and automaticity as a result of slowed atrial, atrioventricular (AV) nodal, His-Purkinje, and intraventricular conduction. It causes a slight but significant prolongation of refractory periods in these tissues. The greatest effect is on the His-Purkinje syste...
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Mechanism of Action: Encainide is a sodium channel blocker, binding to voltage gated sodium channels. It stabilizes the neuronal membrane by inhibiting the ionic fluxes required for the initiation and conduction of impulses. Ventricular excitability is depressed and the stimulation threshold of the ventricle is increased during diastole.
Route of elimination: A radiolabeled dose of encainide is excreted in approximately equal amounts in the urine and feces.
Half Life: 1-2 hours
Affected organisms: Humans and other mammals
Interactions
Drug interaction:
CisaprideIncreased risk of cardiotoxicity and arrhythmias

Targets


Enzymes