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

Details

Stereochemistry ACHIRAL
Molecular Formula C17H18N2O5S
Molecular Weight 362.4
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIRETANIDE

SMILES

NS(=O)(=O)C1=C(OC2=CC=CC=C2)C(=CC(=C1)C(O)=O)N3CCCC3

InChI

InChIKey=UJEWTUDSLQGTOA-UHFFFAOYSA-N
InChI=1S/C17H18N2O5S/c18-25(22,23)15-11-12(17(20)21)10-14(19-8-4-5-9-19)16(15)24-13-6-2-1-3-7-13/h1-3,6-7,10-11H,4-5,8-9H2,(H,20,21)(H2,18,22,23)

HIDE SMILES / InChI

Molecular Formula C17H18N2O5S
Molecular Weight 362.4
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:29:52 UTC 2023
Edited
by admin
on Sat Dec 16 17:29:52 UTC 2023
Record UNII
DQ6KK6GV93
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIRETANIDE
EP   INN   JAN   MART.   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
PIRETANIDE [MART.]
Common Name English
ARELIX
Brand Name English
HOE 118
Code English
BENZOIC ACID, 3-(AMINOSULFONYL)-4-PHENOXY-5-(1-PYRROLIDINYL)-
Common Name English
PIRETANIDE [MI]
Common Name English
S-73-4118
Code English
PIRETANIDE [EP MONOGRAPH]
Common Name English
4-PHENOXY-3-(PYRROLIDINYL)-5-SULFAMOYLBENZOIC ACID
Systematic Name English
PIRETANIDE [USAN]
Common Name English
PIRETANIDE [JAN]
Common Name English
S-734118
Code English
piretanide [INN]
Common Name English
HOE-118
Code English
Piretanide [WHO-DD]
Common Name English
S 73 4118
Code English
Classification Tree Code System Code
WHO-VATC QC03CA03
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
WHO-ATC C03CA03
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
NCI_THESAURUS C49184
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
Code System Code Type Description
SMS_ID
100000081664
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
EVMPD
SUB09906MIG
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
CAS
55837-27-9
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
DRUG CENTRAL
2201
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
FDA UNII
DQ6KK6GV93
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
ECHA (EC/EINECS)
259-852-9
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
EPA CompTox
DTXSID2023488
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
DRUG BANK
DB02925
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
RXCUI
33770
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY RxNorm
MESH
C015451
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
WIKIPEDIA
PIRETANIDE
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
MERCK INDEX
m8875
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY Merck Index
INN
3741
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
ChEMBL
CHEMBL349803
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
PUBCHEM
4849
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
NCI_THESAURUS
C66419
Created by admin on Sat Dec 16 17:29:52 UTC 2023 , Edited by admin on Sat Dec 16 17:29:52 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY