CHEBI:55548 - sulfamoxole

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ChEBI Name sulfamoxole
Definition A sulfonamide antibiotic in which 4-aminobenzenesulfonic acid and 4,5-dimethyl-1,3-oxazol-2-amine have combined to form the sulfonamide bond.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C11H13N3O3S
Net Charge 0
Average Mass 267.30400
Monoisotopic Mass 267.068
InChI InChI=1S/C11H13N3O3S/c1-7-8(2)17-11(13-7)14-18(15,16)10-5-3-9(12)4-6-10/h3-6H,12H2,1-2H3,(H,13,14)
SMILES Cc1nc(NS(=O)(=O)c2ccc(N)cc2)oc1C
Roles Classification
Biological Role(s): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
(via sulfonamide antibiotic )
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ChEBI Ontology
Outgoing sulfamoxole (CHEBI:55548) has role antimicrobial agent (CHEBI:33281)
sulfamoxole (CHEBI:55548) is a oxazole (CHEBI:35790)
sulfamoxole (CHEBI:55548) is a sulfonamide (CHEBI:35358)
sulfamoxole (CHEBI:55548) is a sulfonamide antibiotic (CHEBI:87228)
INNs Sources
sulfamoxol ChemIDplus
sulfamoxole ChemIDplus
sulfamoxolum ChemIDplus
Synonyms Sources
2-(p-Aminobenzenesulfonamido)-4,5-dimethyloxazole ChemIDplus
2-(p-Aminobenzolsulfonamido)-4,5-dimethyloxazol ChemIDplus
4,5-Dimethyl-2-sulfanilamidooxazole ChemIDplus
4-Amino-N-(4,5-dimethyl-2-oxazolyl)benzenesulfonamide ChemIDplus
N(sup 1)-(4,5-Dimethyl-2-oxazolyl)sulfanilamide ChemIDplus
N1-(4,5-Dimethyl-2-oxazolyl)sulfanilamide ChemIDplus
Oxasulfa ChemIDplus
p-Aminobenzenesulfonyl-2-amino-4,5-dimethyloxazole ChemIDplus
Sulfadimethyloxazole ChemIDplus
Sulphamoxole ChemIDplus
Manual Xrefs Databases
2520 DrugCentral
DB08798 DrugBank
View more database links
Registry Numbers Types Sources
248434 Beilstein Registry Number Beilstein
729-99-7 CAS Registry Number ChemIDplus
729-99-7 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
13882073 PubMed citation Europe PMC
13888264 PubMed citation Europe PMC
3237218 PubMed citation Europe PMC
3876325 PubMed citation Europe PMC
9886437 PubMed citation Europe PMC
Last Modified
22 February 2017