Dicloxacillin
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Also known as BRL-1702DicloxacilinaDicloxacillineR-13423SID124893598
Summary
Dicloxacillin (CHEMBL893) is an approved small-molecule antibacterial drug (ATC J01CF01); indicated across 4 conditions including bacterial infectious disease and gram-positive bacterial infections.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: J01CF01
- Indications: 4 conditions
- Clinical trials: 7
- Chemistry: 470.3 Da · C19H17Cl2N3O5S
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL893 |
| Name | Dicloxacillin |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 18381 |
| ChEBI | CHEBI:4511 |
| ATC | J01CF01 |
| Molecular formula | C19H17Cl2N3O5S |
| Molecular weight | 470.3 |
| InChIKey | YFAGHNZHGGCZAX-JKIFEVAISA-N |
SMILES: CC1=C(C(=NO1)C2=C(C=CC=C2Cl)Cl)C(=O)N[C@H]3[C@@H]4N(C3=O)[C@H](C(S4)(C)C)C(=O)O
IUPAC name: (2S,5R,6R)-6-[[3-(2,6-dichlorophenyl)-5-methyl-1,2-oxazole-4-carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
ChEBI definition: A penicillin that is 6-aminopenicillanic acid in which one of the amino hydrogens is replaced by a 3-(2,6-dichlorophenyl)-5-methyl-1,2-oxazol-4-yl]formyl group.
Pharmacological roles (ChEBI): antibacterial drug.
Also known as: BRL-1702, Dicloxacilina, Dicloxacillin, Dicloxacilline, R-13423, dicloxacillin, DICLOXACILLIN, SID124893598, DICLOXACILLINE
Parent form; salt/anhydrous children: CHEMBL26570, CHEMBL1200701
Patent coverage: 6,475 distinct patent families (26,391 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: Organic anion transporter 3, Bile salt export pump.
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 (1 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 |
| bacterial infectious disease with sepsis | 3 | MONDO:0005229 | EFO:0003033 |
| gram-positive bacterial infections | 3 | MONDO:0021679 | MONDO:0021679 |
| osteomyelitis | 0 | MONDO:0005246 | EFO:0003102 |
Clinical trials
Total trials: 7.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 3 |
| PHASE1 | 2 |
| PHASE3 | 1 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05398679 | PHASE4 | RECRUITING | Oral Antimicrobial Treatment vs. Outpatient Parenteral for Infective Endocarditis |
| NCT05156437 | PHASE4 | TERMINATED | Postoperative Antibiotic Management Duration Following Surgery for Intravenous Drug Abuse (IVDA) Endocarditis (OPTIMAL) |
| NCT05578482 | PHASE4 | UNKNOWN | Staphylococcus Aureus and The Skin Microbiome During Flare And Resolution Of Atopic Dermatitis |
| NCT00037050 | PHASE3 | COMPLETED | Antibiotic Treatment for Infections of Short Term In-dwelling Vascular Catheters Due to Gram Positive Bacteria |
| NCT02983890 | PHASE1 | COMPLETED | Dicloxacillin: Clinical Relevance of Drug-drug Interactions by Induction of Drug Metabolism. |
| NCT05073627 | PHASE1 | COMPLETED | The Effect of Dicloxacillin on Oral Absorption of Drugs |
| NCT00162474 | Not specified | RECRUITING | Determinants of Warfarin Metabolism |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline, but PharmGKB curates 2 clinical and 3 variant annotation(s) for this drug (gene-keyed; see PharmGKB).
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).