Rifalazil
drugOn this page
Also known as KRM-1648RifalaziloNA
Summary
Rifalazil (CHEMBL236297) is a phase-3 clinical-stage small molecule; indicated across 2 conditions including intermittent vascular claudication and chlamydia trachomatis infectious disease.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- Indications: 2 conditions
- Clinical trials: 3
- Chemistry: 941.1 Da · C51H64N4O13
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL236297 |
| Name | Rifalazil |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 135431094 |
| Molecular formula | C51H64N4O13 |
| Molecular weight | 941.1 |
| InChIKey | IXSVOCGZBUJEPI-HTQYORAHSA-N |
SMILES: C[C@H]1/C=C/C=C(\C(=O)NC2=C3C(=C4C(=C(C(=C5C4=C([C@](O5)(O/C=C/[C@@H]([C@H]([C@H]([C@@H]([C@@H]([C@@H]([C@H]1O)C)O)C)OC(=O)C)C)OC)C)O)C)O)C2=O)N=C6C(=CC(=CC6=O)N7CCN(CC7)CC(C)C)O3)/C
IUPAC name: [(7S,9E,11S,12R,13S,14R,15R,16R,17S,18S,19E,21Z)-2,6,15,17-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-30-[4-(2-methylpropyl)piperazin-1-yl]-23,32,37-trioxo-8,27,38-trioxa-24,34-diazahexacyclo[23.11.1.14,7.05,36.026,35.028,33]octatriaconta-1,3,5,9,19,21,25,28,30,33,35-undecaen-13-yl] acetate
Also known as: KRM-1648, Rifalazil, Rifalazilo, rifalazil, RIFALAZIL, NA
Patent coverage: 414 distinct patent families (1,513 SureChEMBL compound mentions), from 3 matched compound structure(s). One matched structure accounts for 1,488 (98%) of the total. 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: DNA-directed RNA polymerase subunit beta.
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
2 indications (0 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 |
|---|---|---|---|
| intermittent vascular claudication | 3 | MONDO:0005295 | EFO:0003876 |
| chlamydia trachomatis infectious disease | 2 | MONDO:0005701 | EFO:0007205 |
Clinical trials
Total trials: 3.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE2 | 2 |
| PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00251849 | PHASE3 | UNKNOWN | PROVIDENCE-1: Study of Rifalazil in Chlamydia Pneumoniae Seropositive Patients |
| NCT00385385 | PHASE2 | UNKNOWN | RESTORE-IT-Study of Rifalazil in Chlamydia Pneumoniae Seropositive Patients With a History of Atherosclerotic Disease |
| NCT01631201 | PHASE2 | COMPLETED | Safety and Efficacy Study of Rifalazil for the Treatment of Chlamydia Trachomatis Infection in Women |
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).
Related Atlas pages
- Diseases: intermittent vascular claudication