Josamycin
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Also known as EN-141IosalideJomybelJosamicinaJosaminaJosamycin propionateJosamycineKitasamycin a3Leucomycin a3Turimycin a5
Summary
Josamycin (CHEMBL224436) is a phase-3 clinical-stage small-molecule antibacterial drug (ATC J01FA07); indicated across 2 conditions including bacterial infectious disease.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- ATC class: J01FA07
- Indications: 2 conditions
- Clinical trials: 1
- Chemistry: 828 Da · C42H69NO15
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL224436 |
| Name | Josamycin |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 5282165 |
| ChEBI | CHEBI:31739 |
| ATC | J01FA07 |
| Molecular formula | C42H69NO15 |
| Molecular weight | 828 |
| InChIKey | XJSFLOJWULLJQS-NGVXBBESSA-N |
SMILES: C[C@@H]1C/C=C/C=C/[C@@H]([C@@H](C[C@@H]([C@@H]([C@H]([C@@H](CC(=O)O1)OC(=O)C)OC)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)OC(=O)CC(C)C)(C)O)N(C)C)O)CC=O)C)O
IUPAC name: [(2S,3S,4R,6S)-6-[(2R,3S,4R,5R,6S)-6-[[(4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-acetyloxy-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-6-yl]oxy]-4-(dimethylamino)-5-hydroxy-2-methyloxan-3-yl]oxy-4-hydroxy-2,4-dimethyloxan-3-yl] 3-methylbutanoate
ChEBI definition: A macrolide antibiotic produced by certain strains of Streptomyces narbonensis var. josamyceticus.
Pharmacological roles (ChEBI): antibacterial drug.
Other ChEBI roles (chemical / environmental): metabolite.
Also known as: EN-141, Iosalide, Jomybel, Josamicina, Josamina, Josamycin, Josamycin propionate, Josamycine, Kitasamycin a3, Leucomycin a3, Turimycin a5, josamycin
Patent coverage: 2,526 distinct patent families (9,073 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: 1 (assay-derived). Sample: Bacterial 70S ribosome.
Bioactivity
ChEMBL activities: 1 potent at pChembl ≥ 5 of 1 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| P02358 | 5.92 | IC50 | 1200 | nM | CHEMBL_ACT_14611103 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
1 disease in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.
| Disease (in trials) | Phase | MONDO | EFO |
|---|---|---|---|
| bacterial infectious disease | 3 | MONDO:0005113 | EFO:0000771 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 1.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00718705 | PHASE3 | COMPLETED | Reduction of Spontaneous Prematurity by Antibiotic Treatment (Josamycin) |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- In clinical trials for: bacterial infectious disease