CHEBI:77092 - fenbendazole

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ChEBI Name fenbendazole
ChEBI ID CHEBI:77092
Definition A member of the class of benzimidazoles that is 1H-benzimidazole which is substituted at positons 2 and 5 by (methoxycarbonyl)amino and phenylsulfanediyl groups, respectively. A broad-spectrum anthelmintic, it is used, particularly in veterinary medicine, for the treatment of nematodal infections.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C15H13N3O2S
Net Charge 0
Average Mass 299.34800
Monoisotopic Mass 299.073
InChI InChI=1S/C15H13N3O2S/c1-20-15(19)18-14-16-12-8-7-11(9-13(12)17-14)21-10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19)
InChIKey HDDSHPAODJUKPD-UHFFFAOYSA-N
SMILES COC(=O)Nc1nc2cc(Sc3ccccc3)ccc2[nH]1
Roles Classification
Application(s): antinematodal drug
A substance used in the treatment or control of nematode infestations.
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ChEBI Ontology
Outgoing fenbendazole (CHEBI:77092) has role antinematodal drug (CHEBI:35444)
fenbendazole (CHEBI:77092) is a aryl sulfide (CHEBI:35683)
fenbendazole (CHEBI:77092) is a benzimidazoles (CHEBI:22715)
fenbendazole (CHEBI:77092) is a carbamate ester (CHEBI:23003)
Incoming hydroxyfenbendazole (CHEBI:140184) has functional parent fenbendazole (CHEBI:77092)
oxfendazole (CHEBI:35812) has functional parent fenbendazole (CHEBI:77092)
IUPAC Name
methyl [5-(phenylsulfanyl)-1H-benzimidazol-2-yl]carbamate
INNs Sources
fenbendazol WHO MedNet
fenbendazole WHO MedNet
fenbendazole WHO MedNet
fenbendazolum WHO MedNet
Synonyms Sources
2-(methoxycarbonylamino)-5-(phenylthio)benzimidazole ChemIDplus
5-(phenylthio)-2-benzimidazolecarbamic acid methyl ester ChEBI
[5-(phenylthio)-1H-benzimidazol-2-yl]carbamic acid methyl ester ChEBI
fenbendazole UniProt
Hoe 881v ChemIDplus
methyl 5-(phenylthio)-2-benzimidazolecarbamate ChemIDplus
methyl [5-(phenylthio)-1H-benzimidazol-2-yl]carbamate ChemIDplus
Brand Names Sources
Panacur ChemIDplus
Safe-quard ChemIDplus
Manual Xrefs Databases
1758 VSDB
4536 DrugCentral
D04140 KEGG DRUG
DE2164690 Patent
Fenbendazole Wikipedia
HMDB0029745 HMDB
LSM-3134 LINCS
US3954791 Patent
View more database links
Registry Numbers Types Sources
43210-67-9 CAS Registry Number ChemIDplus
759077 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
22048645 PubMed citation Europe PMC
23488766 PubMed citation Europe PMC
23959307 PubMed citation Europe PMC
24183965 PubMed citation Europe PMC
Last Modified
26 February 2018