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

Details

Stereochemistry RACEMIC
Molecular Formula C9H12ClN3O4S2
Molecular Weight 325.792
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHIAZIDE

SMILES

CCC1NC2=CC(Cl)=C(C=C2S(=O)(=O)N1)S(N)(=O)=O

InChI

InChIKey=VXLCNTLWWUDBSO-UHFFFAOYSA-N
InChI=1S/C9H12ClN3O4S2/c1-2-9-12-6-3-5(10)7(18(11,14)15)4-8(6)19(16,17)13-9/h3-4,9,12-13H,2H2,1H3,(H2,11,14,15)

HIDE SMILES / InChI

Molecular Formula C9H12ClN3O4S2
Molecular Weight 325.792
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Ethiazide is a diuretic.

Originator

Curator's Comment: Now is a part of Mitsubishi Tanabe Pharma.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Interaction of benzothiadiazides with human serum albumin studied by dialysis and spectroscopic methods.
1994-10
Epimerization and racemization of some chiral drugs in the presence of human serum albumin.
1990-01
Epimerization and racemization of some chiral drugs in the presence of cyclodextrin and liposomes.
1989-10
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:02:30 GMT 2025
Edited
by admin
on Mon Mar 31 18:02:30 GMT 2025
Record UNII
EK9LSW731R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHIAZIDE [JAN]
Preferred Name English
ETHIAZIDE
INN   JAN   MI   WHO-DD  
INN  
Official Name English
Ethiazide [WHO-DD]
Common Name English
ETHIAZIDE [MI]
Common Name English
6-CHLORO-3-ETHYL-3,4-DIHYDRO-2H-1,2,4-BENZOTHIADIAZINE-7-SULFONAMIDE-1,1-DIOXIDE
Systematic Name English
ethiazide [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C49185
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
Code System Code Type Description
INN
1648
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
PRIMARY
EVMPD
SUB07275MIG
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
PRIMARY
ChEMBL
CHEMBL2106262
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
PRIMARY
SMS_ID
100000082597
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
PRIMARY
NCI_THESAURUS
C80840
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
PRIMARY
PUBCHEM
15763
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
PRIMARY
CAS
1824-58-4
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
PRIMARY
MERCK INDEX
m723
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
PRIMARY Merck Index
FDA UNII
EK9LSW731R
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID1046215
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
217-358-0
Created by admin on Mon Mar 31 18:02:30 GMT 2025 , Edited by admin on Mon Mar 31 18:02:30 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY