ChemicalBook--->CAS DataBase List--->56010-88-9

56010-88-9

56010-88-9 Structure

56010-88-9 Structure
IdentificationBack Directory
[Name]

4-METHYLPYRAZOLE HYDROCHLORIDE
[CAS]

56010-88-9
[Synonyms]

FOMEPIZOLE HYDROCHLORIDE
4-METHYLPYRAZOLE HYDROCHLORIDE
Fomepizole/FomepizolechlorideHCl
4-Methyl-1H-pyrazole hydrochloride
4-Methylpyrazole hydrochloride alcohol dehydrogenase inhibitor
[Molecular Formula]

C4H7ClN2
[MDL Number]

MFCD00012707
[MOL File]

56010-88-9.mol
[Molecular Weight]

118.56
Chemical PropertiesBack Directory
[Melting point ]

157-159 °C
[storage temp. ]

2-8°C
[solubility ]

methanol: 100mg/mL, clear, colorless to yellow
[form ]

powder
[color ]

Purple to purplish red
[biological source]

synthetic (organic)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

4-Methylpyrazole hydrochloride has been used:
  • as a cytochrome P450 2E1 inhibitor
  • as cytochrome P450 2E1 and alcohol dehydrogenase inhibitor in 1C11 neural progenitor cells
  • to inhibit ethanol oxidation in VL-17A cells expressing alcohol dehydrogenase and HepG2 cells

[Biochem/physiol Actions]

4-Methylpyrazole (4MP) inhibits ethanol oxidation in liver microsomes. It also blocks the c-Jun N-terminal kinase (JNK) activation in in vitro liver injury models.
[in vivo]

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

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).
[IC 50]

CYP2E1
Spectrum DetailBack Directory
[Spectrum Detail]

4-METHYLPYRAZOLE HYDROCHLORIDE(56010-88-9)Raman
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