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CHEBI:5141 - fomepizole

ChEBI IDCHEBI:5141
ChEBI Namefomepizole
Stars
DefinitionA member of the class of pyrazoles that is 1H-pyrazole substituted by a methyl group at position 4.
Last Modified22 February 2017
DownloadsMolfile
FormulaC4H6N2
Net Charge0
Average Mass82.106
Monoisotopic Mass82.05310
SMILESCc1cnnc1
InChIInChI=1S/C4H6N2/c1-4-2-5-6-3-4/h2-3H,1H3,(H,5,6)
InChIKeyRIKMMFOAQPJVMX-UHFFFAOYSA-N
Wikipedia
Roles Classification
Biological Role:
EC 1.1.1.1 (alcohol dehydrogenase) inhibitor  An EC 1.1.1.* (oxidoreductase acting on donor CH-OH group, NAD+ or NADP+ acceptor) inhibitor that interferes with the action of alcohol dehydrogenase (EC 1.1.1.1).
Applications:
protective agent  Synthetic or natural substance which is given to prevent a disease or disorder or are used in the process of treating a disease or injury due to a poisonous agent.
antidote  Any protective agent counteracting or neutralizing the action of poisons.
ChEBI Ontology
Outgoing Relation(s)
fomepizole (CHEBI:5141) has parent hydride 1H-pyrazole (CHEBI:17241)
fomepizole (CHEBI:5141) has role antidote (CHEBI:50247)
fomepizole (CHEBI:5141) has role EC 1.1.1.1 (alcohol dehydrogenase) inhibitor (CHEBI:50269)
fomepizole (CHEBI:5141) has role protective agent (CHEBI:50267)
fomepizole (CHEBI:5141) is a pyrazoles (CHEBI:26410)
IUPAC Name 
4-methyl-1H-pyrazole
INNs  Source
fomepizolDrugBank
fomepizoleDrugBank
fomepizolumDrugBank
Synonyms  Source
4-MethylpyrazolChemIDplus
4-MethylpyrazoleKEGG COMPOUND
Brand Name  Source
AntizolDrugBank
Manual XrefsDatabases
1233DrugCentral
4PZPDBeChem
C07837KEGG COMPOUND
D00707KEGG DRUG
DB01213DrugBank
FomepizoleWikipedia
HMDB0015344HMDB
LSM-5671LINCS
Registry NumbersSources
Reaxys:105204Reaxys
CAS:7554-65-6KEGG COMPOUND
CAS:7554-65-6NIST Chemistry WebBook
CAS:7554-65-6ChemIDplus
Citations