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Fomepizole

产品号 DB01213 公司名称 DrugBank
CAS号 7554-65-6 公司网站 http://www.ualberta.ca/
分子式 C4H6N2 电 话 (780) 492-3111
分子量 82.10384 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 1083

产品价格信息

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产品别名

标题
Fomepizole
IUPAC标准名
4-methyl-1H-pyrazole
IUPAC传统名
fomepizole
商标名
Antizol
别名
Fomepizol [INN-Spanish]
Fomepizolum [INN-Latin]
Fomepizole [USAN:INN]
4-methylpyrazole

产品登记号

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

产品性质

疏水性(logP) 0.9

产品详细信息

详细说明 (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
Wikipedia
RxList
Drugs.com

参考文献