CHEBI:88258 - sulfametrole

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ChEBI Name sulfametrole
ChEBI ID CHEBI:88258
Definition A sulfonamide obtained by formal condensation of the sulfo group of 4-aminobenzenesulfonic acid with the amino group of 4-methoxy-1,2,5-thiadiazol-3-amine.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C9H10N4O3S2
Net Charge 0
Average Mass 286.333
Monoisotopic Mass 286.01943
InChI InChI=1S/C9H10N4O3S2/c1-16-9-8(11-17-12-9)13-18(14,15)7-4-2-6(10)3-5-7/h2-5H,10H2,1H3,(H,11,13)
InChIKey IZOYMGQQVNAMHS-UHFFFAOYSA-N
SMILES S(=O)(=O)(NC1=NSN=C1OC)C2=CC=C(N)C=C2
Metabolite of Species Details
Bacillus methanolicus MGA3 (NCBI:txid796606) See: MetaboLights Study
Bacillus methanolicus MGA3 (NCBI:txid796606) See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
(via sulfonamide antibiotic )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing sulfametrole (CHEBI:88258) has parent hydride 1,2,5-thiadiazole (CHEBI:39469)
sulfametrole (CHEBI:88258) is a aromatic ether (CHEBI:35618)
sulfametrole (CHEBI:88258) is a substituted aniline (CHEBI:48975)
sulfametrole (CHEBI:88258) is a sulfonamide antibiotic (CHEBI:87228)
sulfametrole (CHEBI:88258) is a thiadiazoles (CHEBI:38099)
IUPAC Name
4-amino-N-(4-methoxy-1,2,5-thiadiazol-3-yl)benzene-1-sulfonamide
INNs Sources
sulfametrol ChemIDplus
sulfametrole ChemIDplus
sulfametrole ChemIDplus
sulfametrolum ChemIDplus
Synonym Source
N1-(4-Methoxy-1,2,5-thiadiazol-3-yl)sulfanilamide ChemIDplus
Manual Xrefs Databases
2518 DrugCentral
D08541 KEGG DRUG
Sulfametrole Wikipedia
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Registry Numbers Types Sources
32909-92-5 CAS Registry Number KEGG DRUG
32909-92-5 CAS Registry Number ChemIDplus
813310 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
24257317 PubMed citation Europe PMC
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Last Modified
22 February 2017