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Details

Stereochemistry RACEMIC
Molecular Formula C25H35NO5
Molecular Weight 429.5491
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEBEVERINE

SMILES

CCN(CCCCOC(=O)C1=CC=C(OC)C(OC)=C1)C(C)CC2=CC=C(OC)C=C2

InChI

InChIKey=VYVKHNNGDFVQGA-UHFFFAOYSA-N
InChI=1S/C25H35NO5/c1-6-26(19(2)17-20-9-12-22(28-3)13-10-20)15-7-8-16-31-25(27)21-11-14-23(29-4)24(18-21)30-5/h9-14,18-19H,6-8,15-17H2,1-5H3

HIDE SMILES / InChI

Molecular Formula C25H35NO5
Molecular Weight 429.5491
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: description was created based on several sources, including: http://www.mhra.gov.uk/home/groups/par/documents/websiteresources/con744437.pdf | https://www.ncbi.nlm.nih.gov/pubmed/20128021

Mebeverine is an antispasmodic with a direct action on the smooth muscle of the gastrointestinal tract. The exact mechanism of action is not known, but multiple mechanisms, such as a decrease in ion channel permeabilities, blockade of noradrenaline reuptake, a local anesthetic effects, as well as weak anti-muscarinic and phosphodiesterase inhibitory effect might contribute to the local effects of Mebeverine. This medicine is used to treat symptoms of irritable bowel syndrome (IBS) and similar problems such as chronic irritable colon, spastic constipation, mucous colitis and spastic colitis. Most people will not have problems with Mebeverine, but some may get some side effects, such as: difficulty in breathing, swelling of face, neck, tongue or throat, skin rash, red itchy skin.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Alpha-1 adrenergic receptor (guinea pig)
Target ID: Muscarinic acetylcholine receptors (guinea pig)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
Colofac

Approved Use

Colofac is used to treat symptoms of irritable bowel syndrome and similar problems.

Launch Date

1978
Palliative
Colofac

Approved Use

This medicine is used to treat symptoms of irritable bowel syndrome (IBS) and similar problems such as chronic irritable colon, spastic constipation, mucous colitis and spastic colitis.

Launch Date

1978
Palliative
Colofac

Approved Use

This medicine is used to treat symptoms of irritable bowel syndrome (IBS) and similar problems such as chronic irritable colon, spastic constipation, mucous colitis and spastic colitis

Launch Date

1978
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
685.28 ng/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
O-DESMETHYL MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
28.79 ng/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
6.61 ng/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
1-BUTANOL, 4-(ETHYL(2-(4-METHOXYPHENYL)-1-METHYLETHYL)AMINO)- plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
62.52 ng/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
291.81 ng/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
O-DESMETHYL MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
7669.41 ng × h/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
O-DESMETHYL MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
339.21 ng × h/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
47.57 ng × h/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
1-BUTANOL, 4-(ETHYL(2-(4-METHOXYPHENYL)-1-METHYLETHYL)AMINO)- plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
365.85 ng × h/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
2551.74 ng × h/mL
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
O-DESMETHYL MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
7.39 h
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
O-DESMETHYL MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
15.78 h
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
2.99 h
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
1-BUTANOL, 4-(ETHYL(2-(4-METHOXYPHENYL)-1-METHYLETHYL)AMINO)- plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
2.87 h
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
7.52 h
200 mg single, oral
dose: 200 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
O-DESMETHYL MEBEVERINE ACID plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
16.49%
MEBEVERINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
25.68%
MEBEVERINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
25%
MEBEVERINE plasma
Homo sapiens
Doses

Doses

DosePopulationAdverse events​
270 mg 3 times / day multiple, oral
Highest studied dose
Dose: 270 mg, 3 times / day
Route: oral
Route: multiple
Dose: 270 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Other AEs: Diarrhoea, Anorexia...
Other AEs:
Diarrhoea (grade 1, 1.7%)
Anorexia (grade 2, 1.7%)
Headache (grade 1-2, 3.3%)
Menorrhagia (grade 2, 1.7%)
Palpitation (grade 2, 1.7%)
Alopecia (grade 1, 1.7%)
Cystitis (grade 2, 3.3%)
Sources:
50 mg single, intravenous
Highest studied dose
Dose: 50 mg
Route: intravenous
Route: single
Dose: 50 mg
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Other AEs: Faintness, Dizziness...
Other AEs:
Faintness (7.1%)
Dizziness (14.2%)
Vomiting (7.1%)
Sources:
AEs

AEs

AESignificanceDosePopulation
Alopecia grade 1, 1.7%
270 mg 3 times / day multiple, oral
Highest studied dose
Dose: 270 mg, 3 times / day
Route: oral
Route: multiple
Dose: 270 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Diarrhoea grade 1, 1.7%
270 mg 3 times / day multiple, oral
Highest studied dose
Dose: 270 mg, 3 times / day
Route: oral
Route: multiple
Dose: 270 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Headache grade 1-2, 3.3%
270 mg 3 times / day multiple, oral
Highest studied dose
Dose: 270 mg, 3 times / day
Route: oral
Route: multiple
Dose: 270 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Anorexia grade 2, 1.7%
270 mg 3 times / day multiple, oral
Highest studied dose
Dose: 270 mg, 3 times / day
Route: oral
Route: multiple
Dose: 270 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Menorrhagia grade 2, 1.7%
270 mg 3 times / day multiple, oral
Highest studied dose
Dose: 270 mg, 3 times / day
Route: oral
Route: multiple
Dose: 270 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Palpitation grade 2, 1.7%
270 mg 3 times / day multiple, oral
Highest studied dose
Dose: 270 mg, 3 times / day
Route: oral
Route: multiple
Dose: 270 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Cystitis grade 2, 3.3%
270 mg 3 times / day multiple, oral
Highest studied dose
Dose: 270 mg, 3 times / day
Route: oral
Route: multiple
Dose: 270 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Dizziness 14.2%
50 mg single, intravenous
Highest studied dose
Dose: 50 mg
Route: intravenous
Route: single
Dose: 50 mg
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Faintness 7.1%
50 mg single, intravenous
Highest studied dose
Dose: 50 mg
Route: intravenous
Route: single
Dose: 50 mg
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Vomiting 7.1%
50 mg single, intravenous
Highest studied dose
Dose: 50 mg
Route: intravenous
Route: single
Dose: 50 mg
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
Profiling of a prescription drug library for potential renal drug-drug interactions mediated by the organic cation transporter 2.
2011-07-14
Development of a list of potentially inappropriate drugs for the korean elderly using the delphi method.
2010-12
Management of irritable bowel syndrome in primary care: feasibility randomised controlled trial of mebeverine, methylcellulose, placebo and a patient self-management cognitive behavioural therapy website. (MIBS trial).
2010-11-18
Topical piroxicam in vitro release and in vivo anti-inflammatory and analgesic effects from palm oil esters-based nanocream.
2010-11-04
First derivative synchronous fluorescence spectroscopy for the simultaneous determination of sulpiride and mebeverine hydrochloride in their combined tablets and application to real human plasma.
2010-11
Validated HPLC determination of the two fixed dose combinations (chlordiazepoxide hydrochloride and mebeverine hydrochloride; carvedilol and hydrochlorothiazide) in their tablets.
2010-10-07
Autoimmune hepatitis triggered by nitrofurantoin: a case series.
2010-09-23
Presentations of perforated colonic pathology in patients with polymyalgia rheumatica: two case reports.
2010-09-06
Development and validation of stability indicating HPLC and HPTLC methods for determination of sulpiride and mebeverine hydrochloride in combination.
2010-09
Colloids as a sink for certain pharmaceuticals in the aquatic environment.
2010-05
Predictors of treatment outcome after cognitive behavior therapy and antispasmodic treatment for patients with irritable bowel syndrome in primary care.
2010-04
Design and formulation of mebeverine HCl semisolid formulations for intraorally administration.
2010-03
A systematic review of efficacy and tolerability of mebeverine in irritable bowel syndrome.
2010-02-07
[Modern approaches to the therapy of biliary system diseases].
2010
[A method for non-medicamentous treatment of irritated bowel syndrome].
2009-07-30
pH-Sensitive Mebeverine Microspheres for Colon Delivery.
2009-07
The four killers of Meckel's diverticulum.
2009-05
Validated LC-MS/MS method for determination of Alverine and one of its hydroxy metabolites in human plasma along with its application to a bioequivalence study.
2009-01-15
Development of membrane selective electrode for determination of the antipsychotic sulpiride in pharmaceuticals and urine.
2009
[The effectiveness of spasmolytic therapy in chronic acalculous cholecystitis].
2009
[How to raise efficacy of gastroesophageal reflux disease treatment].
2009
Psychological associations of irritable bowel syndrome besides panic disorder: an often overlooked reality.
2009
Drug use in children: cohort study in three European countries.
2008-11-24
Effect of fibre, antispasmodics, and peppermint oil in the treatment of irritable bowel syndrome: systematic review and meta-analysis.
2008-11-13
Evaluation of the Birmingham IBS symptom questionnaire.
2008-07-23
Effects of 5-hydroxytryptamine (serotonin) type 3 antagonists on symptom relief and constipation in nonconstipated irritable bowel syndrome: a systematic review and meta-analysis of randomized controlled trials.
2008-05
Cost-effectiveness of cognitive behaviour therapy in addition to mebeverine for irritable bowel syndrome.
2008-04
[Irritable bowel syndrome-an unbeloved problem].
2008-03-27
Spectrophotometric determination of benzydamine HCl, levamisole HCl and mebeverine HCl through ion-pair complex formation with methyl orange.
2008-03
Serotonin receptor modulators in the treatment of irritable bowel syndrome.
2008-02
[Efficacy of duspatalin in the treatment and prophylaxis of postcholecystectomic syndrome].
2008
Colon-specific drug delivery for mebeverine hydrochloride.
2007-12
A novel formulation for mebeverine hydrochloride.
2007-10
Improving the detection limits of antispasmodic drugs electrodes by using modified membrane sensors with inner solid contact.
2007-05-09
[Drug treatment of irritable bowel syndrome: an unmet need].
2007-03
Development of in situ ion selective sensors for dissolution.
2007-01-02
[Chronic abdominal pain syndrome in biliary pathology].
2007
Health technology assessment and ill-structured problems: a case study concerning the drug mebeverine.
2007
[Assessment of the efficacy of mebeverine in the complex therapy of chronic noncalculolis cholecystitis and biliary dysfunction].
2007
Formulation of an antispasmodic drug as a topical local anesthetic.
2006-12-01
Cognitive behavioural therapy in addition to antispasmodic therapy for irritable bowel syndrome in primary care: randomised controlled trial.
2006-06
Quality of life of patients with irritable bowel syndrome is low compared to others with chronic diseases.
2006-05
"My patients are the sickest".
2006-05
Mebeverine influences sodium ion transport in the distal colon.
2006-03-15
Investigative implications of the instability and metabolism of mebeverine.
2006-03
[Mebeverine for complex treatment of opisthorchiasis].
2006
[The pain problem as a historic aspect. Pain at the biliary pathology. Mebeverine hydrochloride as a part of complex therapy].
2006
Generic and brand-name drugs. Are different criteria sufficiently taken into account before granting market authorisation?
2006
A new RP-HPLC method for analysis of mebeverine hydrochloride in raw materials and tablets.
2005-04
Rapid accurate mass desorption electrospray ionisation tandem mass spectrometry of pharmaceutical samples.
2005
Patents

Sample Use Guides

One tablet (135 mg) three times a day. This may be gradually reduced after a few weeks when the desired effect has been obtained. The tablets are best taken 20 minutes before meals.
Route of Administration: Oral
In Vitro Use Guide
Mebeverine (10^5-10^4 M) suppressed the amplitude of the action potential and lengthened the time between stimulation and the top of the response in non-myelinated fibres of the vagus nerve.
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:15:57 GMT 2025
Edited
by admin
on Mon Mar 31 18:15:57 GMT 2025
Record UNII
7F80CC3NNV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ARLUY
Preferred Name English
MEBEVERINE
INN   MI   WHO-DD  
INN  
Official Name English
MEBEVERINE [MI]
Common Name English
Mebeverine [WHO-DD]
Common Name English
BENZOIC ACID, 3,4-DIMETHOXY-, 4-(ETHYL(2-(4-METHOXYPHENYL)-1-METHYLETHYL)AMINO)BUTYL ESTER
Common Name English
VERATRIC ACID, 4-((ETHYL(P-METHOXY-.ALPHA.-METHYLPHENETHYL))AMINO)BUTYL ESTER
Common Name English
4-(ETHYL(P-METHOXY-.ALPHA.-METHYLPHENETHYL)AMINO)BUTYL VERATRATE
Common Name English
mebeverine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66880
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
WHO-ATC A03AA04
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
WHO-VATC QA03AA04
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID6023238
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
FDA UNII
7F80CC3NNV
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
DRUG CENTRAL
1642
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
CAS
3625-06-7
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
RXCUI
29410
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY RxNorm
PUBCHEM
4031
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
ECHA (EC/EINECS)
222-830-4
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
SMS_ID
100000081730
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
ChEMBL
CHEMBL282121
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
EVMPD
SUB08662MIG
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
MERCK INDEX
m7108
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY Merck Index
MESH
C005096
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
WIKIPEDIA
MEBEVERINE
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
INN
1191
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
DRUG BANK
DB12554
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
NCI_THESAURUS
C83909
Created by admin on Mon Mar 31 18:15:57 GMT 2025 , Edited by admin on Mon Mar 31 18:15:57 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY