FB2026_03 , released September 17, 2026
Chemical: metronidazole
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General Information
Name
metronidazole
FlyBase ID
FBch0001305
ChEBI Name
metronidazole
ChEBI ID
PubChem Name
Metronidazole
PubChem ID
Chemical Structure
Chemical structure of metronidazole
metronidazole
InChIKey

VAOCPAMSLUNLGC-UHFFFAOYSA-N

Definition (ChEBI)

A member of the class of imidazoles substituted at C-1, -2 and -5 with 2-hydroxyethyl, nitro and methyl groups respectively. It has activity against anaerobic bacteria and protozoa, and has a radiosensitising effect on hypoxic tumour cells. It may be given by mouth in tablets, or as the benzoate in an oral suspension. The hydrochloride salt can be used in intravenous infusions. Metronidazole is a prodrug and is selective for anaerobic bacteria due to their ability to intracellularly reduce the nitro group of metronidazole to give nitroso-containing intermediates. These can covalently bind to DNA, disrupting its helical structure, inducing DNA strand breaks and inhibiting bacterial nucleic acid synthesis, ultimately resulting in bacterial cell death.

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (30)
Synonyms
1-(2-hydroxy-1-ethyl)-2-methyl-5-nitroimidazole
1-(2-hydroxyethyl)-2-methyl-5-nitroimidazole
1-(beta-ethylol)-2-methyl-5-nitro-3-azapyrrole
1-(beta-hydroxyethyl)-2-methyl-5-nitroimidazole
1-(beta-oxyethyl)-2-methyl-5-nitroimidazole
2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethanol
2-Methyl-5-nitroimidazole-1-ethanol
2-methyl-1-(2-hydroxyethyl)-5-nitroimidazole
2-methyl-3-(2-hydroxyethyl)-4-nitroimidazole
2-methyl-5-nitroimidazole-1-ethanol
443-48-1
Anagiardil
Bayer 5360
Gineflavir
MetroGel
Metronidazol
PubChem:4173
Trichazol
anagiardil
bayer 5360
gineflavir
metrogel
metronidazolum
pubchem:4173
trichazol
Secondary FlyBase IDs
    References (6)