1. Fomepizole hydrochloride

Fomepizole hydrochloride  (Synonyms: 4-Methylpyrazole hydrochloride)

Cat. No.: HY-B0876A
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Fomepizole (4-Methylpyrazole) hydrochloride is a potent and orally active cytochrome P450 (CYP2E1) inhibitor. Fomepizole hydrochloride is a competitive inhibitor of the enzyme alcohol dehydrogenase. Fomepizole hydrochloride blocks further conversion of methanol and ethylene glycol to toxic metabolites. Fomepizole hydrochloride has the potential for an antidote for ethylene glycol or methanol poisoning.

For research use only. We do not sell to patients.

Fomepizole hydrochloride Chemical Structure

Fomepizole hydrochloride Chemical Structure

CAS No. : 56010-88-9

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Description

Fomepizole (4-Methylpyrazole) hydrochloride is a potent and orally active cytochrome P450 (CYP2E1) inhibitor. Fomepizole hydrochloride is a competitive inhibitor of the enzyme alcohol dehydrogenase. Fomepizole hydrochloride blocks further conversion of methanol and ethylene glycol to toxic metabolites. Fomepizole hydrochloride has the potential for an antidote for ethylene glycol or methanol poisoning[1][2][3].

In Vivo

Pretreatment with Fomepizole (4-Methylpyrazole; 25 mg/kg; IP) prolongs ethanol neurobehavioral toxicity in CD-1 mice[4]

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male CD-1 mice weighing 18-25 g[4]
Dosage: 25 mg/kg
Administration: IP; single dose
Result: Decreased the dose of ethanol (1-5 g/kg; IP) at which 50% of the animals failed a particular outcome test (toxic dose 50; TD50).
Clinical Trial
Molecular Weight

118.56

Formula

C4H7ClN2

CAS No.
SMILES

CC1=CNN=C1.[H]Cl

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Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

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Fomepizole hydrochloride
Cat. No.:
HY-B0876A
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