Metronidazole

CHEMBL137 Phase 4 Одобрено Small molecule
Half-Life
8 hours
Bioavailability
Protein Binding
Molecular Weight
171.2 g/mol
LogP
Phase
4

Reductive activation inside anaerobic organisms converts metronidazole into cytotoxic free radicals that fragment microbial DNA, an activation step that requires the low-redox environment such organisms provide and that explains the drug's selectivity. Its spectrum spans both bacteria and protozoa, supporting use in infections of the digestive tract, the reproductive system and the skin. Warfarin is recorded as a major interaction, the anticoagulant effect being potentiated when the two are given together. An elimination half-life near eight hours accompanies its classification among antiinfectives for systemic use. The molecule is small, C6H9N3O3 at approximately 171.2 g/mol, and reached the final phase of clinical development.

This antibiotic and antiprotozoal drug kills bacteria and parasites by damaging their DNA. It is used to treat a wide range of infections including those of the digestive tract, reproductive system, and skin.

Молекулярная масса

171,1540 g/mol

LogP

0,00

TPSA

83,90 Ų

Правило пяти Липинского

Соответствует

Терапевтические области

Классы препаратов

Pharmacokinetics (PK)

Half-Life 8 hours

Pharmacodynamics (PD)

2D Структура

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SMILES

Cc1ncc([N+](=O)[O-])n1CCO

InChI

InChI=1S/C6H9N3O3/c1-5-7-4-6(9(11)12)8(5)2-3-10/h4,10H,2-3H2,1H3

Molecular Formula

C6H9N3O3

HBD / HBA

1 / 4

Вращаемые Связи

2

Тяжёлые Атомы

12

No targets recorded

Target interaction data is not yet available for this drug.

No side effects recorded

Side effect data is not yet available for this drug.

Часто задаваемые вопросы

This antibiotic and antiprotozoal drug kills bacteria and parasites by damaging their DNA. It is used to treat a wide range of infections including those of the digestive tract, reproductive system, and skin.

Key pharmacokinetic parameters for Metronidazole: Half-life: 8 hours.

Yes, Metronidazole is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

Related Drugs

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL137. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 4173. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-08-20.

Медицинский отказ от ответственности

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.