Discuss This Drug

Tinidazole

CHEBI:CHEBI_63627

Definition

1H-imidazole substituted at C-1 by a (2-ethylsulfonyl)ethyl group, at C-2 by a methyl group and at C-5 by a nitro group. It is used as an antiprotozoal, antibacterial agent.

Chemical Information

Molecular Formula
C8H13N3O4S
Molecular Mass
247.27200
Charge
0
SMILES
CCS(=O)(=O)CCn1c(C)ncc1[N+]([O-])=O
InChI
InChI=1S/C8H13N3O4S/c1-3-16(14,15)5-4-10-7(2)9-6-8(10)11(12)13/h6H,3-5H2,1-2H3
InChIKey
HJLSLZFTEKNLFI-UHFFFAOYSA-N

Alternative Names

  • 1-[2-(ethylsulfonyl)ethyl]-2-methyl-5-nitro-1H-imidazole
  • timidazole

Drug Classification

Important Medical Information

⚕️ This information is sourced from ChEBI (Chemical Entities of Biological Interest) database and is intended for educational purposes only.

  • Always consult with a healthcare professional before starting, stopping, or modifying any medication.
  • Side effects may vary and this list may not be comprehensive.
  • Drug interactions may occur with other medications.

Additional Identifiers

DRON_00010000
10612
core#notation
CHEBI:63627
oboInOwl#hasDbXref
Wikipedia:Tinidazole

Additional References

Wikipedia:Tinidazole

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Additional Attributes

oboInOwl#hasOBONamespace
chebi_ontology
DRON_00010000
10612
oboInOwl#hasAlternativeId
CHEBI:32227
oboInOwl#id
CHEBI:63627
core#notation
CHEBI:63627
oboInOwl#hasDbXref
Wikipedia:Tinidazole
RO_0000087
http://purl.obolibrary.org/obo/CHEBI_36047
oboInOwl#inSubset
http://purl.obolibrary.org/obo/chebi#3_STAR
22-rdf-syntax-ns#type
http://www.w3.org/2002/07/owl#Class
has_treatment
http://purl.obolibrary.org/obo/DOID_3767
owl#annotatedSource
t262937
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t945233