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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
Epimerization and racemization of some chiral drugs in the presence of cyclodextrin and liposomes.
1989 Oct
Epimerization and racemization of some chiral drugs in the presence of human serum albumin.
1990 Jan
Interaction of benzothiadiazides with human serum albumin studied by dialysis and spectroscopic methods.
1994 Oct
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 Fri Dec 15 15:35:58 GMT 2023
Edited
by admin
on Fri Dec 15 15:35:58 GMT 2023
Record UNII
EK9LSW731R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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 [JAN]
Common Name English
ethiazide [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C49185
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
Code System Code Type Description
INN
1648
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
PRIMARY
EVMPD
SUB07275MIG
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106262
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
PRIMARY
SMS_ID
100000082597
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
PRIMARY
NCI_THESAURUS
C80840
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
PRIMARY
PUBCHEM
15763
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
PRIMARY
CAS
1824-58-4
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
PRIMARY
MERCK INDEX
m723
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
PRIMARY Merck Index
FDA UNII
EK9LSW731R
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID1046215
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
PRIMARY
ECHA (EC/EINECS)
217-358-0
Created by admin on Fri Dec 15 15:35:58 GMT 2023 , Edited by admin on Fri Dec 15 15:35:58 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY