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CHEBI:32166 - sulfisomidine

ChEBI IDCHEBI:32166
ChEBI Namesulfisomidine
Stars
DefinitionA sulfonamide consisting of pyrimidine having methyl substituents at the 2- and 6-positions and a 4-aminobenzenesulfonamido group at the 4-position.
Last Modified22 February 2017
DownloadsMolfile
FormulaC12H14N4O2S
Net Charge0
Average Mass278.337
Monoisotopic Mass278.08375
SMILESCc1cc(NS(=O)(=O)c2ccc(N)cc2)nc(C)n1
InChIInChI=1S/C12H14N4O2S/c1-8-7-12(15-9(2)14-8)16-19(17,18)11-5-3-10(13)4-6-11/h3-7H,13H2,1-2H3,(H,14,15,16)
InChIKeyYZMCKZRAOLZXAZ-UHFFFAOYSA-N
Roles Classification
Biological Role:
antimicrobial agent  A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
Application:
antiinfective agent  A substance used in the prophylaxis or therapy of infectious diseases.
ChEBI Ontology
Outgoing Relation(s)
sulfisomidine (CHEBI:32166) has functional parent sulfanilamide (CHEBI:45373)
sulfisomidine (CHEBI:32166) has role antiinfective agent (CHEBI:35441)
sulfisomidine (CHEBI:32166) is a pyrimidines (CHEBI:39447)
sulfisomidine (CHEBI:32166) is a sulfonamide (CHEBI:35358)
sulfisomidine (CHEBI:32166) is a sulfonamide antibiotic (CHEBI:87228)
IUPAC Name 
4-amino-N-(2,6-dimethylpyrimidin-4-yl)benzenesulfonamide
INNs  Source
solfisomidinaChemIDplus
sulfaisodimidinumChemIDplus
Synonyms  Source
SulfaisodimidineKEGG DRUG
(p-Aminobenzolsulfonyl)-4-amino-2,6-dimethylpyrimidinChemIDplus
2,4-Dimethyl-6-sulfanilamidopyrimidineChemIDplus
2,6-Dimethyl-4-sulfanilamidopyrimidineChemIDplus
4-Sulfa-2,6-dimethylpyrimidineChemIDplus
4-Sulfanilamido-2,6-dimethylpyrimidineChemIDplus
Manual XrefsDatabases
D01526KEGG DRUG
FR886009Patent
US2351333Patent
US2386852Patent
US2429184Patent
2526DrugCentral
Registry NumbersSources
Beilstein:261305Beilstein
CAS:515-64-0KEGG DRUG
CAS:515-64-0ChemIDplus
CAS:515-64-0NIST Chemistry WebBook
Citations