CHEBI:41231 - N-benzyl-4-sulfamoylbenzamide

ChEBI IDCHEBI:41231
ChEBI NameN-benzyl-4-sulfamoylbenzamide
Stars
ASCII NameN-benzyl-4-sulfamoylbenzamide
DefinitionA secondary carboxamide resulting from the formal condensation of the carboxy group of 4-sulfamoylbenzoic acid with the amino group of 1-phenylmethanamine. It is a potent inhibitor of carbonic anhydrase II.
Last Modified31 May 2022
DownloadsMolfile
FormulaC14H14N2O3S
Net Charge0
Average Mass290.344
Monoisotopic Mass290.07251
SMILESNS(=O)(=O)c1ccc(C(=O)NCc2ccccc2)cc1
InChIInChI=1S/C14H14N2O3S/c15-20(18,19)13-8-6-12(7-9-13)14(17)16-10-11-4-2-1-3-5-11/h1-9H,10H2,(H,16,17)(H2,15,18,19)
InChIKeyCZKNSZUJCJHTTM-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Colletotrichum sublineola (ncbitaxon:1173701) - PubMed (30824820) Species also known as Colletotrichum sublineolum.
Roles Classification
Biological Roles:
fungal metabolite  Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
EC 4.2.1.1 (carbonic anhydrase) inhibitor  An EC 4.2.1.* (hydro-lyases) inhibitor that interferes with the action of carbonic anhydrase (EC 4.2.1.1). Such compounds reduce the secretion of H+ ions by the proximal kidney tubule.
ChEBI Ontology
Outgoing Relation(s)
N-benzyl-4-sulfamoylbenzamide (CHEBI:41231) has role EC 4.2.1.1 (carbonic anhydrase) inhibitor (CHEBI:23018)
N-benzyl-4-sulfamoylbenzamide (CHEBI:41231) has role fungal metabolite (CHEBI:76946)
N-benzyl-4-sulfamoylbenzamide (CHEBI:41231) is a benzamides (CHEBI:22702)
N-benzyl-4-sulfamoylbenzamide (CHEBI:41231) is a benzenes (CHEBI:22712)
N-benzyl-4-sulfamoylbenzamide (CHEBI:41231) is a secondary carboxamide (CHEBI:140325)
N-benzyl-4-sulfamoylbenzamide (CHEBI:41231) is a sulfonamide (CHEBI:35358)
IUPAC Name 
N-benzyl-4-sulfamoylbenzamide
Synonyms  Source
N-benzyl-4-sulfamoyl-benzamidePDBeChem
4-(aminosulfonyl)-N-benzylbenzamideChEBI
N-benzyl-4-(aminosulfonyl)benzamideChEBI
4-(benzylcarbamoyl)benzenesulfonamideChEBI
Manual XrefsDatabases
BSBPDBeChem
DB01748DrugBank
4194ChemSpider
Registry NumbersSources
CAS:107619-27-2ChEBI
Citations