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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NO4S
Molecular Weight 201.2
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARZENIDE

SMILES

NS(=O)(=O)C1=CC=C(C=C1)C(O)=O

InChI

InChIKey=UCAGLBKTLXCODC-UHFFFAOYSA-N
InChI=1S/C7H7NO4S/c8-13(11,12)6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)(H2,8,11,12)

HIDE SMILES / InChI

Molecular Formula C7H7NO4S
Molecular Weight 201.2
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

PubMed

PubMed

TitleDatePubMed
Interaction-dependent PCR: identification of ligand-target pairs from libraries of ligands and libraries of targets in a single solution-phase experiment.
2010-11-10
Titration calorimetry standards and the precision of isothermal titration calorimetry data.
2009-06-18
Label-free determination of protein-ligand binding constants using mass spectrometry and validation using surface plasmon resonance and isothermal titration calorimetry.
2009-04-18
Using ion channel-forming peptides to quantify protein-ligand interactions.
2008-01-30
Implementation of chemometric methodology in ACE: predictive investigation of protein-ligand binding.
2007-08
Anti-mycobacterial activity of a bis-sulfonamide.
2007-03-01
Synthesis and structure-activity relationships of novel benzene sulfonamides with potent binding affinity for bovine carbonic anhydrase II.
2005-12-15
Synthesis of 4,5-diaryl-1H-pyrazole-3-ol derivatives as potential COX-2 inhibitors.
2004-10-15
The ABRF-MIRG'02 study: assembly state, thermodynamic, and kinetic analysis of an enzyme/inhibitor interaction.
2003-12
Carbonic anhydrase inhibitors: inhibition of the tumor-associated isozyme IX with aromatic and heterocyclic sulfonamides.
2003-03-24
Back to basics.
2002-07-15
Direct comparison of binding equilibrium, thermodynamic, and rate constants determined by surface- and solution-based biophysical methods.
2002-05
Biodegradation of p-toluenesulphonamide by a Pseudomonas sp.
2001-11-13
Carbonic anhydrase inhibitors: 4-sulfamoyl-benzenecarboxamides and 4-chloro-3-sulfamoyl-benzenecarboxamides with strong topical antiglaucoma properties.
2001-07-09
Design and synthesis of benzoic acid derivatives as influenza neuraminidase inhibitors using structure-based drug design.
1997-12-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:55:11 GMT 2025
Edited
by admin
on Mon Mar 31 17:55:11 GMT 2025
Record UNII
30Z5HQB5A4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-22976
Preferred Name English
CARZENIDE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
P-SULFAMOYLBENZOIC ACID
Common Name English
CARZENIDE [MART.]
Common Name English
4-SULFAMOLYBENZOIC ACID
Common Name English
Carzenide [WHO-DD]
Common Name English
CARZENIDE [MI]
Common Name English
carzenide [INN]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 677403
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C166618
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
SMS_ID
100000081352
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
INN
334
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
MERCK INDEX
m3146
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY Merck Index
MESH
C001910
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
RXCUI
20355
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY RxNorm
FDA UNII
30Z5HQB5A4
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
NSC
22976
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID1045089
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-327-4
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
PUBCHEM
8739
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
CAS
138-41-0
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
EVMPD
SUB06156MIG
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
ChEMBL
CHEMBL414
Created by admin on Mon Mar 31 17:55:11 GMT 2025 , Edited by admin on Mon Mar 31 17:55:11 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY