CHEBI:81927 - enilconazole

ChEBI IDCHEBI:81927
ChEBI Nameenilconazole
Stars
DefinitionA racemate comprising equimolar amounts of (R)- and (S)-enilconazole. A fungicide used to control a wide range of fungi including Tilletia and Helminthosporium spp. on fruit, vegetables and ornamentals. In veterinary medicine, it is used topically for the treatment of fungal skin infections in cattle, dogs, and horses; it is also used by inhalation for the treatment of aspergillosis in ostriches.
Last Modified22 February 2017
FormulaC14H14Cl2N2O
Net Charge0
Average Mass297.180
Monoisotopic Mass296.04832
Wikipedia
Roles Classification
Biological Roles:
EC 1.14.13.70 (sterol 14alpha-demethylase) inhibitor  An EC 1.14.13.* (oxidoreductase acting on paired donors, incorporating 1 atom of oxygen, with NADH or NADPH as one donor) inhibitor that interferes with the action of EC 1.14.13.70 (sterol 14α-demethylase).
antifungal agrochemical  Any substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties.
fungicide  A substance used to destroy fungal pests.
ergosterol biosynthesis inhibitor  Any compound that inhibits one or more steps in the pathway leading to the synthesis of ergosterol.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
fungicide  A substance used to destroy fungal pests.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
antifungal drug  Any antifungal agent used to prevent or treat fungal infections in humans or animals.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
antifungal drug  Any antifungal agent used to prevent or treat fungal infections in humans or animals.
ergosterol biosynthesis inhibitor  Any compound that inhibits one or more steps in the pathway leading to the synthesis of ergosterol.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
ergosterol biosynthesis inhibitor  Any compound that inhibits one or more steps in the pathway leading to the synthesis of ergosterol.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
Applications:
antifungal agrochemical  Any substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties.
fungicide  A substance used to destroy fungal pests.
fungicide  A substance used to destroy fungal pests.
antifungal drug  Any antifungal agent used to prevent or treat fungal infections in humans or animals.
antifungal drug  Any antifungal agent used to prevent or treat fungal infections in humans or animals.
ChEBI Ontology
Outgoing Relation(s)
enilconazole (CHEBI:81927) has part (R)-enilconazole (CHEBI:83831)
enilconazole (CHEBI:81927) has part (S)-enilconazole (CHEBI:83830)
enilconazole (CHEBI:81927) has role antifungal agrochemical (CHEBI:86328)
enilconazole (CHEBI:81927) has role EC 1.14.13.70 (sterol 14α-demethylase) inhibitor (CHEBI:77884)
enilconazole (CHEBI:81927) is a conazole antifungal drug (CHEBI:87071)
enilconazole (CHEBI:81927) is a conazole fungicide (CHEBI:87067)
enilconazole (CHEBI:81927) is a imidazole antifungal drug (CHEBI:87069)
enilconazole (CHEBI:81927) is a imidazole fungicide (CHEBI:87068)
enilconazole (CHEBI:81927) is a racemate (CHEBI:60911)
IUPAC Name 
rac-1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]-1H-imidazole
INNs  Source
enilconazoleKEGG DRUG
enilconazolumWHO MedNet
enilconazolWHO MedNet
énilconazoleWHO MedNet
Synonyms  Source
ImazalilKEGG COMPOUND
Allyl-1-(2,4-dichlorophenyl)-2-imidazol-1-ylethyl etherHMDB
(+-)-1-(beta-(Allyloxy)-2,4-dichlorophenethyl)-imidazoleHMDB
1-[2-(2,4-Dichlorophenyl)-2-(2-propenyloxy)ethyl]-1H-imidazoleHMDB
R 23979ChemIDplus
R 23,979ChemIDplus
Manual XrefsDatabases
D03997KEGG DRUG
C18739KEGG COMPOUND
HMDB0031794HMDB
EnilconazoleWikipedia
imazalilAlan Wood's Pesticides
Registry NumbersSources
Reaxys:545683Reaxys
CAS:35554-44-0KEGG COMPOUND
CAS:35554-44-0ChemIDplus
CAS:35554-44-0NIST Chemistry WebBook
Citations