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Bretylium

Catalog No. DB01158 Name DrugBank
CAS Number 59-41-6 Website http://www.ualberta.ca/
M. F. C11H17BrN+ Telephone (780) 492-3111
M. W. 243.16338 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 1029

SYNONYMS

IUPAC name
[(2-bromophenyl)methyl](ethyl)dimethylazanium
IUPAC Traditional name
bretylium
Brand Name
Bretylan
Ornid
Bretylol
Darenthin
Darentin
Synonyms
Bretylium tolsylate
Bretylium p-toluenesulfonate
Bretylium tosylate
Bretylate
Bretylum

DATABASE IDS

PubChem CID 2431
PubChem SID 46505320
CAS Number 59-41-6

PROPERTIES

Solubility Freely soluble

DETAILS

Description (English)
Item Information
Drug Groups approved
Description Bretylium blocks the release of noradrenaline from the peripheral sympathetic nervous system, and is used in emergency medicine, cardiology, and other specialties for the acute management of ventricular tachycardia and ventricular fibrillation. The primary mode of action for bretylium is thought to be inhibition of voltage-gated K(+) channels. Recent evidence has shown that bretylium may also inhibit the Na,K-ATPase by binding to the extracellular K-site.
Indication For use in the prophylaxis and therapy of ventricular fibrillation. Also used in the treatment of life-threatening ventricular arrhythmias, such as ventricular tachycardia, that have failed to respond to adequate doses of a first-line antiarrhythmic agent, such as lidocaine.
Pharmacology Bretylium is a bromobenzyl quaternary ammonium compound which selectively accumulates in sympathetic ganglia and their postganglionic adrenergic neurons where it inhibits norepinephrine release by depressing adrenergic nerve terminal excitability. Bretylium also suppresses ventricular fibrillation and ventricular arrhythmias.
Toxicity Oral, mouse: LD50 = 400 mg/kg. In the presence of life-threatening arrhythmias, underdosing with bretylium probably presents a greater risk to the patient than potential overdosage. However, one case of accidental overdose has been reported in which a rapidly injected intravenous bolus of 30 mg/kg was given instead of an intended 10 mg/kg dose during an episode of ventricular tachycardia. Marked hypertension resulted, followed by protracted refractory hypotension. The patient expired 18 hours later in asystole, complicated by renal failure and aspiration pneumonitis. Bretylium serum levels were 8000 ng/mL.
Affected Organisms
Humans and other mammals
Biotransformation No metabolites have been identified following administration in man and laboratory animals.
Half Life The terminal half-life in four normal volunteers averaged 7.8±0.6 hours (range 6.9-8.1). During hemodialysis, this patient's arterial and venous bretylium concentrations declined rapidly, resulting in a half-life of 13 hours.
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REFERENCES