Ramatroban
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Also known as BAY-U-3405BaynasEN-137774SID50112772SID144206069SID170465980SID174006902
Summary
Ramatroban (CHEMBL361812) is an approved small molecule targeting PTGDR2; indicated across 2 conditions including asthma and severe acute respiratory syndrome.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- Targets: 1 (PTGDR2)
- Indications: 2 conditions
- Clinical trials: 2
- Chemistry: 416.5 Da · C21H21FN2O4S
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL361812 |
| Name | Ramatroban |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 123879 |
| Molecular formula | C21H21FN2O4S |
| Molecular weight | 416.5 |
| InChIKey | LDXDSHIEDAPSSA-OAHLLOKOSA-N |
SMILES: C1CC2=C(C[C@@H]1NS(=O)(=O)C3=CC=C(C=C3)F)C4=CC=CC=C4N2CCC(=O)O
IUPAC name: 3-[(3R)-3-[(4-fluorophenyl)sulfonylamino]-1,2,3,4-tetrahydrocarbazol-9-yl]propanoic acid
Also known as: BAY-U-3405, Baynas, EN-137774, Ramatroban, ramatroban, SID50112772, SID144206069, SID170465980, SID174006902, RAMATROBAN
Patent coverage: 809 distinct patent families (3,250 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 3,212 (99%) 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
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| PTGDR2 | DP2 receptor | Antagonist | 8.1 | 0% | Q9Y5Y4 |
Broader ChEMBL bioactivity targets: 7 (assay-derived). Sample: Cholecystokinin receptor type A, D(1A) dopamine receptor, Thromboxane A2 receptor, Cytochrome P450 2C9, Prostaglandin D2 receptor, Prostaglandin D2 receptor 2, Bile salt export pump.
Bioactivity
ChEMBL activities: 25 potent at pChembl ≥ 5 of 30 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| TBXA2R | 9.24 | Ki | 0.58 | nM | CHEMBL_ACT_5134848 |
| PTGDR2 | 8.37 | Ki | 4.3 | nM | CHEMBL_ACT_1516936 |
| TBXA2R | 8.35 | Ki | 4.5 | nM | CHEMBL_ACT_1516939 |
| TBXA2R | 8.08 | IC50 | 8.4 | nM | CHEMBL_ACT_1516941 |
| TBXA2R | 8.02 | IC50 | 9.6 | nM | CHEMBL_ACT_1516940 |
| TBXA2R | 7.85 | IC50 | 14 | nM | CHEMBL_ACT_2706511 |
| TBXA2R | 7.75 | Ki | 18 | nM | CHEMBL_ACT_1428603 |
| PTGDR2 | 7.68 | IC50 | 21 | nM | CHEMBL_ACT_2714937 |
| PTGDR2 | 7.55 | IC50 | 28 | nM | CHEMBL_ACT_1516938 |
| PTGDR2 | 7.54 | IC50 | 29 | nM | CHEMBL_ACT_1516937 |
| TBXA2R | 7.51 | AC50 | 31.1 | nM | CHEMBL_ACT_25155526 |
| TBXA2R | 7.4 | AC50 | 40 | nM | CHEMBL_ACT_25198237 |
| PTGDR2 | 7.14 | Ki | 73 | nM | CHEMBL_ACT_2714934 |
| PTGDR2 | 7.11 | IC50 | 77 | nM | CHEMBL_ACT_5314871 |
| PTGDR2 | 6.86 | Ki | 137 | nM | CHEMBL_ACT_5134840 |
| PTGDR2 | 6.77 | IC50 | 169 | nM | CHEMBL_ACT_2153957 |
| PTGDR2 | 6.71 | IC50 | 195 | nM | CHEMBL_ACT_2714938 |
| PTGDR2 | 6.68 | IC50 | 210 | nM | CHEMBL_ACT_2714935 |
| PTGDR2 | 6.54 | Ki | 290 | nM | CHEMBL_ACT_1428599 |
| PTGDR2 | 6.54 | Ki | 290 | nM | CHEMBL_ACT_1428600 |
| PTGDR2 | 6.51 | IC50 | 311 | nM | CHEMBL_ACT_2706463 |
| PTGDR2 | 6.47 | Ki | 340 | nM | CHEMBL_ACT_1428601 |
| PTGDR2 | 6.34 | IC50 | 461 | nM | CHEMBL_ACT_5295534 |
| PTGDR2 | 6.12 | IC50 | 754 | nM | CHEMBL_ACT_2706475 |
| DRD1 | 5.22 | AC50 | 6010 | nM | CHEMBL_ACT_25114827 |
Target pathways
Aggregated over 1 target gene(s): PTGDR2.
Top Reactome pathways
2 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Prostanoid ligand receptors | 1 | PTGDR2 |
| G alpha (i) signalling events | 1 | PTGDR2 |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| chemotaxis | 1 |
| immune response | 1 |
| G protein-coupled receptor signaling pathway | 1 |
| adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway | 1 |
| neuropeptide signaling pathway | 1 |
| calcium-mediated signaling | 1 |
| positive regulation of G protein-coupled receptor signaling pathway | 1 |
| cellular response to prostaglandin D stimulus | 1 |
| negative regulation of male germ cell proliferation | 1 |
| signal transduction | 1 |
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 |
|---|---|---|---|
| asthma | 2 | MONDO:0004979 | MONDO:0004979 |
| severe acute respiratory syndrome | 2 | MONDO:0005091 | MONDO:0100096 |
Clinical trials
Total trials: 2.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE2/PHASE3 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05706454 | PHASE2/PHASE3 | RECRUITING | Phase 2/Phase 3 Study To Evaluate The Efficacy And Safety Of Ramatroban Along With The Standard Of Care In Subjects Hospitalized For COVID Pneumonia |
| NCT00311051 | PHASE2/PHASE3 | WITHDRAWN | Ramatroban/Montelukast Versus Montelukast/Placebo on the Early Allergic Reaction in Asthma Sensitive to House Dust Mite |
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
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
10 molecules share ≥1 primary target. Top 10 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| INDOMETHACIN | ChEMBL + PubChem | Phase 4 (approved) | PTGDR2 |
| LAROPIPRANT | ChEMBL | Phase 4 (approved) | PTGDR2 |
| FEVIPIPRANT | ChEMBL | Phase 3 | PTGDR2 |
| SETIPIPRANT | ChEMBL | Phase 3 | PTGDR2 |
| TIMAPIPRANT | ChEMBL | Phase 3 | PTGDR2 |
| AZD1981 | ChEMBL | Phase 2 | PTGDR2 |
| BI-671800 | ChEMBL | Phase 2 | PTGDR2 |
| FENTIAZAC | ChEMBL | Phase 2 | PTGDR2 |
| QAV680 | ChEMBL | Phase 2 | PTGDR2 |
| VIDUPIPRANT | ChEMBL | Phase 2 | PTGDR2 |
Related Atlas pages
- Genes: PTGDR2
- Drugs: Indomethacin, Laropiprant, Fevipiprant, Setipiprant, Timapiprant