Ebastine
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Also known as EbastinaLAS W-090LAS-W-090RP 64305RP-64305SID26758025SID90340626SID144205778SID170465995
Summary
Ebastine (CHEMBL305660) is an approved small molecule (ATC R06AX22); indicated across 2 conditions including allergic disease and irritable bowel syndrome.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: R06AX22
- Indications: 2 conditions
- Clinical trials: 6
- Chemistry: 469.7 Da · C32H39NO2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL305660 |
| Name | Ebastine |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 3191 |
| ATC | R06AX22 |
| Molecular formula | C32H39NO2 |
| Molecular weight | 469.7 |
| InChIKey | MJJALKDDGIKVBE-UHFFFAOYSA-N |
SMILES: CC(C)(C)C1=CC=C(C=C1)C(=O)CCCN2CCC(CC2)OC(C3=CC=CC=C3)C4=CC=CC=C4
IUPAC name: 4-(4-benzhydryloxypiperidin-1-yl)-1-(4-tert-butylphenyl)butan-1-one
Also known as: Ebastina, Ebastine, LAS W-090, LAS-W-090, RP 64305, RP-64305, SID26758025, SID90340626, EBASTINE, SID144205778, SID170465995, ebastine
Patent coverage: 2,689 distinct patent families (10,024 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: 54 (assay-derived). Sample: Nuclear receptor ROR-gamma, Prelamin-A/C, 4’-phosphopantetheinyl transferase ffp, NPC intracellular cholesterol transporter 1, Ras-related protein Rab-9A, Muscarinic acetylcholine receptor M4, Receptor tyrosine-protein kinase erbB-2, 5-hydroxytryptamine receptor 2B, Tyrosine-protein kinase Fyn, Alpha-2A adrenergic receptor.
Bioactivity
ChEMBL activities: 87 potent at pChembl ≥ 5 of 103 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| HRH1 | 8.48 | Ki | 3.29 | nM | CHEMBL_ACT_7647745 |
| HTR2A | 7.59 | Ki | 25.8 | nM | CHEMBL_ACT_7649845 |
| PRKAA2 | 7.58 | Ki | 26 | nM | CHEMBL_ACT_25872880 |
| HRH1 | 7.55 | IC50 | 28.3 | nM | CHEMBL_ACT_7647744 |
| ADRA2C | 7.4 | Ki | 40.1 | nM | CHEMBL_ACT_7647647 |
| DRD3 | 7.38 | Ki | 41.3 | nM | CHEMBL_ACT_7647715 |
| P31389 | 7.35 | IC50 | 45 | nM | CHEMBL_ACT_576827 |
| HTR1A | 7.33 | IC50 | 47 | nM | CHEMBL_ACT_576831 |
| DRD2 | 7.21 | IC50 | 61 | nM | CHEMBL_ACT_576832 |
| SLC6A3 | 7.11 | Ki | 78.4 | nM | CHEMBL_ACT_7647719 |
| KCNH2 | 7.07 | Ki | 85.8 | nM | CHEMBL_ACT_7649803 |
| HTR2A | 7.04 | IC50 | 90.4 | nM | CHEMBL_ACT_7649844 |
| SLC6A3 | 7.01 | IC50 | 98.7 | nM | CHEMBL_ACT_7647718 |
| CHRM1 | 7 | Ki | 101.2 | nM | CHEMBL_ACT_7647773 |
| KCNH2 | 6.98 | IC50 | 104.8 | nM | CHEMBL_ACT_7649802 |
| CHRM4 | 6.94 | Ki | 115.5 | nM | CHEMBL_ACT_7647779 |
| DRD3 | 6.92 | IC50 | 121.6 | nM | CHEMBL_ACT_7647714 |
| HTR2C | 6.91 | Ki | 124.4 | nM | CHEMBL_ACT_7649849 |
| CHRM3 | 6.86 | Ki | 137.2 | nM | CHEMBL_ACT_7647777 |
| MLNR | 6.8 | AC50 | 160 | nM | CHEMBL_ACT_25189046 |
| ADRA1D | 6.74 | IC50 | 183 | nM | CHEMBL_ACT_576828 |
| HTR2B | 6.7 | Ki | 198.9 | nM | CHEMBL_ACT_7649847 |
| P15823 | 6.63 | Ki | 232.9 | nM | CHEMBL_ACT_7647639 |
| CHRM5 | 6.62 | Ki | 242.7 | nM | CHEMBL_ACT_7649771 |
| HTR2C | 6.62 | IC50 | 237.5 | nM | CHEMBL_ACT_7649848 |
| ADRA2C | 6.56 | IC50 | 275.7 | nM | CHEMBL_ACT_7647646 |
| CHRM2 | 6.55 | Ki | 279.5 | nM | CHEMBL_ACT_7647775 |
| ADRA2A | 6.51 | Ki | 311.9 | nM | CHEMBL_ACT_7647643 |
| HTR2B | 6.5 | IC50 | 312.6 | nM | CHEMBL_ACT_7649846 |
| KCNH2 | 6.48 | IC50 | 331.1 | nM | CHEMBL_ACT_5218942 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
2 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 |
|---|---|---|---|
| allergic disease | 4 | MONDO:0005271 | MONDO:0005271 |
| irritable bowel syndrome | 3 | MONDO:0005052 | EFO:0000555 |
Clinical trials
Total trials: 6.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 3 |
| PHASE3 | 1 |
| PHASE2/PHASE3 | 1 |
| PHASE1/PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01144832 | PHASE4 | COMPLETED | Irritable Bowel Syndrome (IBS) Treatment With H1-receptor Antagonists |
| NCT01908465 | PHASE4 | COMPLETED | Peripheral Histamine 1 Receptor Blockade in IBS: Multicenter Trial |
| NCT01940393 | PHASE4 | COMPLETED | Evaluation of the Inhibitory Effect of 5 Anti-Histamines in Urticaria |
| NCT05815602 | PHASE3 | RECRUITING | Ebastine Versus Mebeverine in IBS Patients |
| NCT07114055 | PHASE2/PHASE3 | RECRUITING | Effect of Ebastine in Patients With Diarrhea Predominant Irritable Bowel Syndrome |
| NCT06480110 | PHASE1/PHASE2 | RECRUITING | Ebastine in Combination With Docetaxel as a Treatment for Castration-resistant Metastatic Prostate Cancer |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline, but PharmGKB curates 0 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).
Related Atlas pages
- Diseases: allergic disease, irritable bowel syndrome