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

Details

Stereochemistry RACEMIC
Molecular Formula C10H11ClF3N3O4S3
Molecular Weight 425.855
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EPITHIAZIDE

SMILES

NS(=O)(=O)C1=C(Cl)C=C2NC(CSCC(F)(F)F)NS(=O)(=O)C2=C1

InChI

InChIKey=RINBGYCKMGDWPY-UHFFFAOYSA-N
InChI=1S/C10H11ClF3N3O4S3/c11-5-1-6-8(2-7(5)23(15,18)19)24(20,21)17-9(16-6)3-22-4-10(12,13)14/h1-2,9,16-17H,3-4H2,(H2,15,18,19)

HIDE SMILES / InChI

Molecular Formula C10H11ClF3N3O4S3
Molecular Weight 425.855
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Epithiazide (epithizide) is a diuretic drug. Its combination with Veriloid under the trade name Thiaver was used in the 1960s for the treatment of hypertension.

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:47:50 GMT 2023
Edited
by admin
on Fri Dec 15 18:47:50 GMT 2023
Record UNII
5B266B85J1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EPITHIAZIDE
MI   USAN  
USAN  
Official Name English
epitizide [INN]
Common Name English
EPITHIAZIDE [USAN]
Common Name English
EPITHIAZIDE [MI]
Common Name English
FLURESE
Brand Name English
THIAVER
Brand Name English
Epitizide [WHO-DD]
Common Name English
P-2105
Code English
EPITIZIDE
INN   MART.   WHO-DD  
INN  
Official Name English
6-Chloro-3,4-dihydro-3{[(2,2,2-trifluoroethyl)thio]methyl}-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
Systematic Name English
3-((2,2,2-TRIFLUOROETHYLTHIO)METHYL)-6-CHLORO-3,4-DIHYDRO-2H-1,2,4-BENZOTHIADIAZINE-7-SULFONAMIDE 1,1-DIOXIDE
Systematic Name English
NSC-108164
Code English
EPITIZIDE [MART.]
Common Name English
Classification Tree Code System Code
WHO-ATC C03EA03
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
NCI_THESAURUS C49185
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
WHO-VATC QC03EA03
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
Code System Code Type Description
CAS
1764-85-8
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104605
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
PUBCHEM
15671
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
MERCK INDEX
m163
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY Merck Index
NSC
108164
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
DRUG CENTRAL
1031
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
INN
1379
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
CAS
96782-87-5
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
SUPERSEDED
DRUG BANK
DB13989
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
NCI_THESAURUS
C77141
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
WIKIPEDIA
EPITIZIDE
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
EPA CompTox
DTXSID50862751
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
FDA UNII
5B266B85J1
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
ECHA (EC/EINECS)
217-181-9
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
SMS_ID
100000080475
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
EVMPD
SUB06573MIG
Created by admin on Fri Dec 15 18:47:50 GMT 2023 , Edited by admin on Fri Dec 15 18:47:50 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY