EPITHIAZIDE

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

Structure Search

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

Approval Year

Name

Type

Language

EPITHIAZIDE

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

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 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

NCI_THESAURUS

C49185

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

WHO-VATC

QC03EA03

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

Code System Code Type Description

CAS

1764-85-8

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

ChEMBL

CHEMBL2104605

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

PUBCHEM

15671

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

MERCK INDEX

m163

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

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Merck Index

NSC

108164

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

DRUG CENTRAL

1031

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

INN

1379

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

CAS

96782-87-5

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

SUPERSEDED

DRUG BANK

DB13989

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

NCI_THESAURUS

C77141

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

WIKIPEDIA

EPITIZIDE

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

EPA CompTox

DTXSID50862751

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

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FDA UNII

5B266B85J1

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

ECHA (EC/EINECS)

217-181-9

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

SMS_ID

100000080475

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

EVMPD

SUB06573MIG

Created by admin on Fri Dec 15 18:47:50 UTC 2023 , Edited by admin on Fri Dec 15 18:47:50 UTC 2023

PRIMARY

ACTIVE MOIETY


					5B266B85J1