Mebeverine

drug
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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

FieldValue
ChEMBL IDCHEMBL282121
NameMebeverine
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID4031
ATCA03AA04
Molecular formulaC25H35NO5
Molecular weight429.5
InChIKeyVYVKHNNGDFVQGA-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):

TargetpChemblTypeValueUnitActivity ID
CYP2D67.6Potency25.1nMCHEMBL_ACT_4998447
CYP2D67.6AC5025.12nMCHEMBL_ACT_5988693
SLC6A46.43AC50370nMCHEMBL_ACT_25151001
CHRM36.22AC50600nMCHEMBL_ACT_25137355
SLC6A36.16AC50700nMCHEMBL_ACT_25124633
CYP3A46.1Potency794.3nMCHEMBL_ACT_4985951
CYP3A46.1Potency794.3nMCHEMBL_ACT_5054976
CYP3A46.1AC50794.3nMCHEMBL_ACT_6049060
KCNH26.02AC50950nMCHEMBL_ACT_25118855
CHRM15.96AC501100nMCHEMBL_ACT_25136157
ADRA2C5.68AC502100nMCHEMBL_ACT_25148575
SLC6A25.6AC502500nMCHEMBL_ACT_25145676
ADRA2A5.55AC502800nMCHEMBL_ACT_25220549
TSHR5.1Potency7943nMCHEMBL_ACT_3915491
OPRK15.02AC509500nMCHEMBL_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).

IndicationTrial phaseMONDOEFO
irritable bowel syndrome3MONDO:0005052EFO: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

PhaseTrials
PHASE42
PHASE32
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00934973PHASE4COMPLETEDManagement of Irritable Bowel Syndrome in Primary Care (MIBS Trial)
NCT05867550PHASE4COMPLETEDTo Compare the Efficacy of Drugs in Combination for Treating Irritable Bowel Syndrome Associated With Diarrhea
NCT04217733PHASE3RECRUITINGEthosuximide and Pentoxifylline in the Treatment of Abdominal Pain Related to Irritable Bowel Syndrome
NCT05175131PHASE3COMPLETEDEfficacy and Safety of Mebeverine + Simethicone in Patients With Functional Bowel Disorders
NCT02260154Not specifiedCOMPLETEDEffectiveness 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.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).