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Details

Stereochemistry RACEMIC
Molecular Formula C13H18ClN3O4S2
Molecular Weight 379.883
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CYCLOPENTHIAZIDE

SMILES

NS(=O)(=O)C1=C(Cl)C=C2NC(CC3CCCC3)NS(=O)(=O)C2=C1

InChI

InChIKey=BKYKPTRYDKTTJY-UHFFFAOYSA-N
InChI=1S/C13H18ClN3O4S2/c14-9-6-10-12(7-11(9)22(15,18)19)23(20,21)17-13(16-10)5-8-3-1-2-4-8/h6-8,13,16-17H,1-5H2,(H2,15,18,19)

HIDE SMILES / InChI

Molecular Formula C13H18ClN3O4S2
Molecular Weight 379.883
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Cyclopenthiazide is a thiazide diuretic. It inhibits the Na+-Cl− symporter in the distal convoluted tubule of the kidney. Cyclopenthiazide is used for the treatment of edema, including that associated with heart failure, and for the treatment of hypertension.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P55017
Gene ID: 6559.0
Gene Symbol: SLC12A3
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
NAVIDREX

Approved Use

Navidrex® 0.5mg Tablets are used to treat high blood pressure and some types of heart problems. They are also used to help reduce fluid retention associated with the pre-menstrual syndrome and some kidney or liver diseases.
Primary
NAVIDREX

Approved Use

Navidrex® 0.5mg Tablets are used to treat high blood pressure and some types of heart problems. They are also used to help reduce fluid retention associated with the pre-menstrual syndrome and some kidney or liver diseases.
Primary
NAVIDREX

Approved Use

Navidrex® 0.5mg Tablets are used to treat high blood pressure and some types of heart problems. They are also used to help reduce fluid retention associated with the pre-menstrual syndrome and some kidney or liver diseases.
PubMed

PubMed

TitleDatePubMed
Letter: Paradoxical effect of pindolol.
1975 Jul 19
Effect of long-term diuretic treatment on body-potassium in heart-disease.
1976 Nov 13
Arrhythmogenic potential of diuretic induced hypokalaemia in patients with mild hypertension and ischaemic heart disease.
1985 Sep
Nicardipine. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy, in the treatment of angina pectoris, hypertension and related cardiovascular disorders.
1987 Apr
Is nifedipine a suitable first-line treatment for essential hypertension in general practice?
1987 Nov
Enalapril-related cholestatic jaundice.
1990 Apr

Sample Use Guides

In Vivo Use Guide
The usual adult dose is half of one tablet (0.25 mg) , or one whole tablet (0.5 mg) a day, alone or with other medicines.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:20:59 UTC 2023
Edited
by admin
on Fri Dec 15 16:20:59 UTC 2023
Record UNII
VX4S2N85F5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CYCLOPENTHIAZIDE
INN   JAN   MART.   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
CYCLOPENTHIAZIDE [MI]
Common Name English
cyclopenthiazide [INN]
Common Name English
6-Chloro-3-(cyclopentylmethyl)-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
Systematic Name English
CYCLOPENTHIAZIDE [JAN]
Common Name English
SU-8341
Code English
CYCLOPENTHIAZIDE [USAN]
Common Name English
NSC-107679
Code English
NAVIDREX
Brand Name English
Cyclopenthiazide [WHO-DD]
Common Name English
CYCLOPENTHIAZIDE [MART.]
Common Name English
2H-1,2,4-BENZOTHIADIAZINE-7-SULFONAMIDE, 6-CHLORO-3-(CYCLOPENTYLMETHYL)-3,4-DIHYDRO-, 1,1-DIOXIDE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C49185
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
WHO-VATC QC03AA07
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
WHO-VATC QC03AB07
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
WHO-ATC C03EA07
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
WHO-ATC C03AA07
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
WHO-VATC QC03EA07
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
WHO-ATC C03AB07
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
Code System Code Type Description
IUPHAR
7899
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
EPA CompTox
DTXSID4022868
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
INN
1230
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
NSC
107679
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
FDA UNII
VX4S2N85F5
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
ChEMBL
CHEMBL1373254
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
DRUG BANK
DB13532
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
MERCK INDEX
m4010
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY Merck Index
EVMPD
SUB06857MIG
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
NCI_THESAURUS
C80839
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
PUBCHEM
2904
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
SMS_ID
100000083754
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
WIKIPEDIA
CYCLOPENTHIAZIDE
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
CAS
742-20-1
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
DRUG CENTRAL
756
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
MESH
D003518
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
ECHA (EC/EINECS)
212-012-5
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY
RXCUI
3000
Created by admin on Fri Dec 15 16:20:59 UTC 2023 , Edited by admin on Fri Dec 15 16:20:59 UTC 2023
PRIMARY RxNorm
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
DEGRADENT -> PARENT
Related Record Type Details
ACTIVE MOIETY