CHEBI:41231 - N-benzyl-4-sulfamoylbenzamide

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ChEBI Name N-benzyl-4-sulfamoylbenzamide
ChEBI ID CHEBI:41231
ChEBI ASCII Name N-benzyl-4-sulfamoylbenzamide
Definition A 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.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C14H14N2O3S
Net Charge 0
Average Mass 290.340
Monoisotopic Mass 290.07251
InChI InChI=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)
InChIKey CZKNSZUJCJHTTM-UHFFFAOYSA-N
SMILES NS(=O)(=O)C1=CC=C(C=C1)C(=O)NCC1=CC=CC=C1
Metabolite of Species Details
Colletotrichum sublineola (NCBI:txid1173701) Species also known as Colletotrichum sublineolum. See: PubMed
Roles Classification
Biological Role(s): 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.
fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 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 Sources
4-(aminosulfonyl)-N-benzylbenzamide ChEBI
4-(benzylcarbamoyl)benzenesulfonamide ChEBI
N-benzyl-4-(aminosulfonyl)benzamide ChEBI
N-benzyl-4-sulfamoyl-benzamide PDBeChem
Manual Xrefs Databases
4194 ChemSpider
BSB PDBeChem
DB01748 DrugBank
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Registry Number Type Source
107619-27-2 CAS Registry Number ChEBI
Citations Waiting for Citations Types Sources
15869279 PubMed citation Europe PMC
17474767 PubMed citation Europe PMC
30824820 PubMed citation Europe PMC
8027991 PubMed citation Europe PMC
Last Modified
31 May 2022
General Comment
2022-05-31 Relevant articles: https://doi.org/10.1039/C5MD00542F