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Fomepizole

Catalog No. DB01213 Name DrugBank
CAS Number 7554-65-6 Website http://www.ualberta.ca/
M. F. C4H6N2 Telephone (780) 492-3111
M. W. 82.10384 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 1083

SYNONYMS

IUPAC name
4-methyl-1H-pyrazole
IUPAC Traditional name
fomepizole
Brand Name
Antizol
Synonyms
Fomepizol [INN-Spanish]
Fomepizolum [INN-Latin]
Fomepizole [USAN:INN]
4-methylpyrazole

DATABASE IDS

CAS Number 7554-65-6
PubChem CID 3406
PubChem SID 46508566

PROPERTIES

Hydrophobicity(logP) 0.9

DETAILS

Description (English)
Item Information
Drug Groups approved
Description Fomepizole is used as an antidote in confirmed or suspected methanol or ethylene glycol poisoning. Fomepizole is a competitive inhibitor of alcohol dehydrogenase, the enzyme that catalyzes the initial steps in the metabolism of ethylene glycol and methanol to their toxic metabolites.
Indication Antizol is indicated as an antidote for ethylene glycol (such as antifreeze) or methanol poisoning, or for use in suspected ethylene glycol or methanol ingestion, either alone or in combination with hemodialysis
Pharmacology Fomepizole is a competitive inhibitor of alcohol dehydrogenase, the enzyme that catalyzes the initial steps in the metabolism of ethylene glycol and methanol to their toxic metabolites. Ethylene glycol is first metabolized to glycoaldehyde which then undergoes further oxidation to glycolate, glyoxylate, and oxalate. It is glycolate and oxalate that are primarily responsible for the metabolic acidosis and renal damage that are seen in ethylene glycol poisoning. {01}{03} Methanol is first metabolized to formaldehyde and then undergoes subsequent oxidation via formaldehyde dehydrogenase to become formic acid. It is formic acid that is primarily responsible for the metabolic acidosis and visual disturbances that are associated with methanol poisoning.
Toxicity Headache, nausea, dizziness
Affected Organisms
Humans and other mammals
Biotransformation Primarily hepaticm the primary metabolite is 4-carboxypyrazole (approximately 80 to 85% of an administered dose). Other metabolites include 4-hydroxymethylpyrazole and the N -glucuronide conjugates of 4-carboxypyrazole and 4-hydroxymethylpyrazole.
Absorption Rapid and complete
Half Life The plasma half-life of Antizol varies with dose, even in patients with normal renal function, and has not been calculated.
Elimination In healthy volunteers, only 1-3.5% of the administered dose of Antizol? (7-20 mg/kg oral and IV) was excreted unchanged in the urine, indicating that metabolism is the major route of elimination. In humans, the primary metabolite of Antizol? is 4-carboxypyrazole (approximately 80-85% of administered dose), which is excreted in the urine. The metabolites of Antizol? are excreted renally.
Distribution * 0.6 to 1.02 L/kg
External Links
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REFERENCES