U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C14H20ClN3O3S
Molecular Weight 345.845
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOPAMIDE

SMILES

C[C@H]1CCC[C@@H](C)N1NC(=O)C2=CC(=C(Cl)C=C2)S(N)(=O)=O

InChI

InChIKey=LBXHRAWDUMTPSE-AOOOYVTPSA-N
InChI=1S/C14H20ClN3O3S/c1-9-4-3-5-10(2)18(9)17-14(19)11-6-7-12(15)13(8-11)22(16,20)21/h6-10H,3-5H2,1-2H3,(H,17,19)(H2,16,20,21)/t9-,10+

HIDE SMILES / InChI

Molecular Formula C14H20ClN3O3S
Molecular Weight 345.845
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Clopamide is a thiazide diuretic which helps in removing fluid from the body. Clopamide is used in treatment of hypertension and edema.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
BRINALDIX

Approved Use

Clopamide is used in treatment of hypertension and excessive fluid retention as in cardiac failure, cirrhosis, chronic renal failure, Nephrotic syndrome, Cushing’s disease.
Primary
BRINALDIX

Approved Use

Clopamide is used in treatment of hypertension and excessive fluid retention as in cardiac failure, cirrhosis, chronic renal failure, Nephrotic syndrome, Cushing’s disease.
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
63 ng/mL
5 mg 0 times / UNKNOWN single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CLOPAMIDE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
543 ng × h/mL
5 mg 0 times / UNKNOWN single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CLOPAMIDE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
11.6 h
5 mg 0 times / UNKNOWN single, oral
dose: 5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CLOPAMIDE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FED
Doses

Doses

DosePopulationAdverse events​
80 mg single, oral
Highest studied dose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M
Food Status: UNKNOWN
Sources:
Other AEs: Nausea, Headache...
Other AEs:
Nausea
Headache
Sources:
5 mg 1 times / day multiple, oral
Recommended
Dose: 5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Disc. AE: Hypokalaemia, Tiredness...
AEs leading to
discontinuation/dose reduction:
Hypokalaemia (2.5%)
Tiredness
Dizziness
Headache
Palpitations
Nausea
Sweating
Anxiety
Bronchial obstruction
Sleep disturbance
Sources:
AEs

AEs

AESignificanceDosePopulation
Headache
80 mg single, oral
Highest studied dose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M
Food Status: UNKNOWN
Sources:
Nausea
80 mg single, oral
Highest studied dose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M
Food Status: UNKNOWN
Sources:
Hypokalaemia 2.5%
Disc. AE
5 mg 1 times / day multiple, oral
Recommended
Dose: 5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Anxiety Disc. AE
5 mg 1 times / day multiple, oral
Recommended
Dose: 5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Bronchial obstruction Disc. AE
5 mg 1 times / day multiple, oral
Recommended
Dose: 5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Dizziness Disc. AE
5 mg 1 times / day multiple, oral
Recommended
Dose: 5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Headache Disc. AE
5 mg 1 times / day multiple, oral
Recommended
Dose: 5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Nausea Disc. AE
5 mg 1 times / day multiple, oral
Recommended
Dose: 5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Palpitations Disc. AE
5 mg 1 times / day multiple, oral
Recommended
Dose: 5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Sleep disturbance Disc. AE
5 mg 1 times / day multiple, oral
Recommended
Dose: 5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Sweating Disc. AE
5 mg 1 times / day multiple, oral
Recommended
Dose: 5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Tiredness Disc. AE
5 mg 1 times / day multiple, oral
Recommended
Dose: 5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 5 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
[Simultaneous determination of five illegal drugs in weight control foods with solid phase extraction-high performance liquid chromatography].
2010-09
Fast gas chromatographic/mass spectrometric determination of diuretics and masking agents in human urine: Development and validation of a productive screening protocol for antidoping analysis.
2006-12-01
High-speed gas chromatography in doping control: fast-GC and fast-GC/MS determination of beta-adrenoceptor ligands and diuretics.
2006-12
Influence of atypical neuroleptics on executive functioning in patients with schizophrenia: a randomized, double-blind comparison of olanzapine vs. clozapine.
2006-04
Screening procedure for detection of diuretics and uricosurics and/or their metabolites in human urine using gas chromatography-mass spectrometry after extractive methylation.
2005-08

Sample Use Guides

Take clopamide on empty stomach 15 min before meals with one full glass of water.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Wed Apr 02 09:30:23 GMT 2025
Edited
by admin
on Wed Apr 02 09:30:23 GMT 2025
Record UNII
17S83WON0I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLOPAMIDE
EP   INN   MART.   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
AQUEX
Preferred Name English
CLOPAMIDE [MART.]
Common Name English
BENZAMIDE, 3-(AMINOSULFONYL)-4-CHLORO-N-(2,6-DIMETHYL-1-PIPERIDINYL)-, CIS-
Common Name English
clopamide [INN]
Common Name English
CLOPAMIDE [MI]
Common Name English
CLOPAMIDE [EP MONOGRAPH]
Common Name English
4-Chloro-N-(2,6-dimethylpiperidino)-3-sulfamoylbenzamide
Systematic Name English
DT-327
Code English
Clopamide [WHO-DD]
Common Name English
CLOPAMIDE [EP IMPURITY]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C49185
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
WHO-VATC QC03BB03
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
WHO-ATC C03BB03
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
WHO-ATC C03BA03
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
WHO-VATC QC03BA03
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
Code System Code Type Description
MESH
D003005
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
DRUG CENTRAL
706
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
ChEMBL
CHEMBL1361347
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
NCI_THESAURUS
C81074
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
ECHA (EC/EINECS)
211-261-7
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
DRUG BANK
DB13792
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
INN
1517
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
RXCUI
2603
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY RxNorm
FDA UNII
17S83WON0I
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
MERCK INDEX
m3652
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY Merck Index
WIKIPEDIA
Clopamide
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
EPA CompTox
DTXSID1022847
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
SMS_ID
100000092324
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
CAS
636-54-4
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
EVMPD
SUB06735MIG
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
PUBCHEM
12492
Created by admin on Wed Apr 02 09:30:23 GMT 2025 , Edited by admin on Wed Apr 02 09:30:23 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY