Mebeverine
drugOn this page
Also known as ArluyMebeverinaSID11112523SID50100996
Summary
Mebeverine (CHEMBL282121) is an approved small molecule (ATC A03AA04); indicated across 2 conditions including irritable bowel syndrome.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: A03AA04
- Indications: 2 conditions
- Clinical trials: 5
- Chemistry: 429.5 Da · C25H35NO5
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL282121 |
| Name | Mebeverine |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 4031 |
| ATC | A03AA04 |
| Molecular formula | C25H35NO5 |
| Molecular weight | 429.5 |
| InChIKey | VYVKHNNGDFVQGA-UHFFFAOYSA-N |
SMILES: CCN(CCCCOC(=O)C1=CC(=C(C=C1)OC)OC)C(C)CC2=CC=C(C=C2)OC
IUPAC name: 4-[ethyl-[1-(4-methoxyphenyl)propan-2-yl]amino]butyl 3,4-dimethoxybenzoate
Also known as: Arluy, Mebeverina, Mebeverine, SID11112523, SID50100996, MEBEVERINE, mebeverine
Parent form; salt/anhydrous children: CHEMBL1446650
Patent coverage: 757 distinct patent families (3,027 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: 19 (assay-derived). Sample: Alpha-2A adrenergic receptor, Alpha-2C adrenergic receptor, Alpha-2B adrenergic receptor, Thyrotropin receptor, Beta-2 adrenergic receptor, 5-hydroxytryptamine receptor 1A, Muscarinic acetylcholine receptor M1, D(2) dopamine receptor, Sodium-dependent noradrenaline transporter, 5-hydroxytryptamine receptor 2A.
Bioactivity
ChEMBL activities: 15 potent at pChembl ≥ 5 of 22 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| CYP2D6 | 7.6 | Potency | 25.1 | nM | CHEMBL_ACT_4998447 |
| CYP2D6 | 7.6 | AC50 | 25.12 | nM | CHEMBL_ACT_5988693 |
| SLC6A4 | 6.43 | AC50 | 370 | nM | CHEMBL_ACT_25151001 |
| CHRM3 | 6.22 | AC50 | 600 | nM | CHEMBL_ACT_25137355 |
| SLC6A3 | 6.16 | AC50 | 700 | nM | CHEMBL_ACT_25124633 |
| CYP3A4 | 6.1 | Potency | 794.3 | nM | CHEMBL_ACT_4985951 |
| CYP3A4 | 6.1 | Potency | 794.3 | nM | CHEMBL_ACT_5054976 |
| CYP3A4 | 6.1 | AC50 | 794.3 | nM | CHEMBL_ACT_6049060 |
| KCNH2 | 6.02 | AC50 | 950 | nM | CHEMBL_ACT_25118855 |
| CHRM1 | 5.96 | AC50 | 1100 | nM | CHEMBL_ACT_25136157 |
| ADRA2C | 5.68 | AC50 | 2100 | nM | CHEMBL_ACT_25148575 |
| SLC6A2 | 5.6 | AC50 | 2500 | nM | CHEMBL_ACT_25145676 |
| ADRA2A | 5.55 | AC50 | 2800 | nM | CHEMBL_ACT_25220549 |
| TSHR | 5.1 | Potency | 7943 | nM | CHEMBL_ACT_3915491 |
| OPRK1 | 5.02 | AC50 | 9500 | nM | CHEMBL_ACT_25130056 |
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 |
|---|---|---|---|
| irritable bowel syndrome | 3 | MONDO:0005052 | EFO:0000555 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 5.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 2 |
| PHASE3 | 2 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00934973 | PHASE4 | COMPLETED | Management of Irritable Bowel Syndrome in Primary Care (MIBS Trial) |
| NCT05867550 | PHASE4 | COMPLETED | To Compare the Efficacy of Drugs in Combination for Treating Irritable Bowel Syndrome Associated With Diarrhea |
| NCT04217733 | PHASE3 | RECRUITING | Ethosuximide and Pentoxifylline in the Treatment of Abdominal Pain Related to Irritable Bowel Syndrome |
| NCT05175131 | PHASE3 | COMPLETED | Efficacy and Safety of Mebeverine + Simethicone in Patients With Functional Bowel Disorders |
| NCT02260154 | Not specified | COMPLETED | Effectiveness of Duspatalin® in Patients With Post-cholecystectomy Gastrointestinal Spasm |
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: irritable bowel syndrome