Ornidazole
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Also known as NSC-95075OrnidazolRO-70207TiberalSID855702SID170466243SID144204133C0164879
Summary
Ornidazole (CHEMBL1449676) is an approved small-molecule antiprotozoal drug (ATC G01AF06); indicated across 4 conditions including bacterial infectious disease and amebiasis.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: G01AF06 (+2 more)
- Indications: 4 conditions
- Clinical trials: 6
- Chemistry: 219.62 Da · C7H10ClN3O3
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1449676 |
| Name | Ornidazole |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 28061 |
| ChEBI | CHEBI:75176 |
| ATC | G01AF06, P01AB03, J01XD03 |
| Molecular formula | C7H10ClN3O3 |
| Molecular weight | 219.62 |
| InChIKey | IPWKIXLWTCNBKN-UHFFFAOYSA-N |
SMILES: CC1=NC=C(N1CC(CCl)O)[N+](=O)[O-]
IUPAC name: 1-chloro-3-(2-methyl-5-nitroimidazol-1-yl)propan-2-ol
ChEBI definition: A C-nitro compound that is 5-nitroimidazole in which the hydrogens at positions 1 and 2 are replaced by 3-chloro-2-hydroxypropyl and methyl groups, respectively. It is used in the treatment of susceptible protozoal infections and for the treatment of anaerobic bacterial infections.
Pharmacological roles (ChEBI): antiprotozoal drug, antiinfective agent, antibacterial drug, antitrichomonal drug, epitope, antiamoebic agent.
Also known as: NSC-95075, Ornidazol, Ornidazole, RO-70207, Tiberal, SID855702, ORNIDAZOLE, SID170466243, SID144204133, C0164879, ornidazole
Patent coverage: 1,900 distinct patent families (5,313 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 2 (assay-derived). Sample: Beta-lactamase, Muscarinic acetylcholine receptor M1.
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
4 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| bacterial infectious disease | 4 | MONDO:0005113 | EFO:0000771 |
| amebiasis | 4 | MONDO:0005644 | EFO:0007144 |
| rectal cancer | 3 | MONDO:0006519 | EFO:1000657 |
| colonic neoplasm | 3 | MONDO:0005401 | MONDO:0021063 |
Clinical trials
Total trials: 6.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 3 |
| Not specified | 2 |
| PHASE4 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06828874 | PHASE4 | COMPLETED | A Study of Levornidazole Disodium Phosphate for Injection vs. Ornidazole in Treatment of Postoperative Intra-Abdominal Infections Caused by Anaerobic Bacteria |
| NCT02618720 | PHASE3 | COMPLETED | Intravenous Versus Combined Oral and Intravenous Antimicrobial Prophylaxis for the Prevention of Surgical Site Infection in Elective Colorectal Surgery |
| NCT03475680 | PHASE3 | TERMINATED | Mechanical Bowel Preparation and Oral Antibiotics Before Colon Cancer Surgery |
| NCT03491540 | PHASE3 | COMPLETED | Mechanical Bowel Preparation and Oral Antibiotics Before Rectal Cancer Surgery |
| NCT06427863 | Not specified | NOT_YET_RECRUITING | Effect of Antibiotic Pretreatment on the Efficacy of WMT in the Treatment of Chronic Constipation |
| NCT06437041 | Not specified | NOT_YET_RECRUITING | Effect of Antibiotic Pretreatment on the Efficacy of WMT in the Treatment of Irritable Bowel Syndrome |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).