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Details

Stereochemistry ACHIRAL
Molecular Formula C16H20N4O3S
Molecular Weight 348.42
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TORSEMIDE

SMILES

CC(C)NC(=O)NS(=O)(=O)C1=CN=CC=C1NC2=CC(C)=CC=C2

InChI

InChIKey=NGBFQHCMQULJNZ-UHFFFAOYSA-N
InChI=1S/C16H20N4O3S/c1-11(2)18-16(21)20-24(22,23)15-10-17-8-7-14(15)19-13-6-4-5-12(3)9-13/h4-11H,1-3H3,(H,17,19)(H2,18,20,21)

HIDE SMILES / InChI
Molecular Formula C16H20N4O3S
Molecular Weight 348.42
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:31:48 UTC 2023
Edited
by admin
on Fri Dec 15 15:31:48 UTC 2023
Record UNII
W31X2H97FB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TORSEMIDE
MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF  
USAN  
Official Name English
LUPRAC
Brand Name English
TORSEMIDE [MI]
Common Name English
TORSEMIDE [USAN]
Common Name English
TORSEMIDE [VANDF]
Common Name English
TORSEMIDE [USP MONOGRAPH]
Common Name English
TORASEMIDE [JAN]
Common Name English
1-ISOPROPYL-3-((4-M-TOLUIDINO-3-PYRIDYL)SULPHONYL)UREA
Systematic Name English
TORSEMIDE [ORANGE BOOK]
Common Name English
TORASEMIDE [EP MONOGRAPH]
Common Name English
torasemide [INN]
Common Name English
Torasemide [WHO-DD]
Common Name English
TORASEMIDE
INN   JAN   MART.   WHO-DD  
INN  
Official Name English
SOAANZ
Brand Name English
TORSEMIDE [USP-RS]
Common Name English
3-PYRIDINESULFONAMIDE, N-(((1-METHYLETHYL)AMINO)CARBONYL)-4-((3-METHYLPHENYL)AMINO)-
Systematic Name English
AC4464
Code English
AC-4464
Code English
TORASEMIDE [MART.]
Common Name English
BM02.015
Code English
BM-02015
Code English
UPCARD
Brand Name English
TORASEMIDE ANHYDROUS [EMA EPAR VETERINARY]
Common Name English
BM-02.015
Code English
TORASEMIDE ANHYDROUS
Common Name English
TORSEMIDE [USP IMPURITY]
Common Name English
Classification Tree Code System Code
WHO-VATC QC03CA04
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
LIVERTOX 984
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
WHO-ATC C03CA04
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
NDF-RT N0000175366
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
NCI_THESAURUS C49184
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
EMA VETERINARY ASSESSMENT REPORTS UPCARD [AUTHORIZED]
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
NDF-RT N0000175590
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
Code System Code Type Description
RS_ITEM_NUM
1672304
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
WIKIPEDIA
TORASEMIDE
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
NCI_THESAURUS
C29506
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
DRUG BANK
DB00214
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
DAILYMED
W31X2H97FB
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
CAS
56211-40-6
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
DRUG CENTRAL
2708
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
ChEMBL
CHEMBL1148
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
EVMPD
SUB11195MIG
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
MESH
C026116
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
IUPHAR
7312
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
CHEBI
9637
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
RXCUI
38413
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY RxNorm
INN
3938
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
EPA CompTox
DTXSID2023690
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
SMS_ID
100000090291
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
PUBCHEM
41781
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
MERCK INDEX
m10981
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY Merck Index
LACTMED
Torsemide
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
FDA UNII
W31X2H97FB
Created by admin on Fri Dec 15 15:31:48 UTC 2023 , Edited by admin on Fri Dec 15 15:31:48 UTC 2023
PRIMARY
Related Record Type Details
SOLUTE CARRIER FAMILY 12 MEMBER 1
TARGET -> INHIBITOR
POTENCY
Structure of TORASEMIDE SODIUM
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of DESISOPROPYL BUTYL TORSEMIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of DESISOPROPYL ETHYL TORSEMIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 4-((3-METHYLPHENYL)AMINO)-3-PYRIDINESULFONAMIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 4-((3-(HYDROXYMETHYL)PHENYL)AMINO)-N-(((1-METHYLETHYL)AMINO)CARBONYL)-3-PYRIDINESULFONAMIDE
IMPURITY -> PARENT
Structure of DESISOPROPYL BUTYL TORSEMIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of ((4-((3-METHYLPHENYL)AMINO)-3-PYRIDINYL)SULFONYL)CARBAMIC ACID ETHYL ESTER
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 4-((3-METHYLPHENYL)AMINO)-3-PYRIDINESULFONAMIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of 3,4-DIHYDRO-4-(3-METHYLPHENYL)-2H-PYRIDO(4,3-E)-1,2,4-THIADIAZINE 1,1-DIOXIDE
IMPURITY -> PARENT
Structure of DESISOPROPYL ETHYL TORSEMIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of 4-(3-METHYLPHENYL)-2H-PYRIDO(4,3-E)-1,2,4-THIADIAZIN-3(4H)-ONE 1,1-DIOXIDE
IMPURITY -> PARENT
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity A = 5.1
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
Structure of TORSEMIDE
ACTIVE MOIETY
NIH
NCATS
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