CHEBI:32166 - sulfisomidine

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ChEBI Name sulfisomidine
ChEBI ID CHEBI:32166
Definition A sulfonamide consisting of pyrimidine having methyl substituents at the 2- and 6-positions and a 4-aminobenzenesulfonamido group at the 4-position.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C12H14N4O2S
Net Charge 0
Average Mass 278.33000
Monoisotopic Mass 278.08375
InChI InChI=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)
InChIKey YZMCKZRAOLZXAZ-UHFFFAOYSA-N
SMILES Cc1cc(NS(=O)(=O)c2ccc(N)cc2)nc(C)n1
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 )
Application(s): antiinfective agent
A substance used in the prophylaxis or therapy of infectious diseases.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 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 Sources
solfisomidina ChemIDplus
sulfaisodimidinum ChemIDplus
Synonyms Sources
(p-Aminobenzolsulfonyl)-4-amino-2,6-dimethylpyrimidin ChemIDplus
(p-Aminobenzolsulfonyl)-4-amino-2,6-dimethylpyrimidine NIST Chemistry WebBook
2,4-Dimethyl-6-sulfanilamidopyrimidine ChemIDplus
2,6-Dimethyl-4-sulfanilamidopyrimidine ChemIDplus
4-Sulfa-2,6-dimethylpyrimidine ChemIDplus
4-Sulfanilamido-2,6-dimethylpyrimidine ChemIDplus
6-(4-Aminobenzenesulfonamido)-2,4-dimethylpyrimidine ChemIDplus
6-(p-Aminobenzenesulfonamido)-2,4-dimethylpyrimidine ChemIDplus
6-(p-Aminobenzenesulfonyl)amino-2,4-dimethylpyrimidine ChemIDplus
6-Sulfanilamido-2,4-dimethylpyrimidine ChemIDplus
N1-(2,6-Dimethyl-4-pyrimidinyl)sulfanilamide NIST Chemistry WebBook
Sulfaisodimidine KEGG DRUG
Sulfasomidine NIST Chemistry WebBook
Sulfisomidine ChemIDplus
Sulphasomidine ChemIDplus
Manual Xrefs Databases
2526 DrugCentral
D01526 KEGG DRUG
FR886009 Patent
US2351333 Patent
US2386852 Patent
US2429184 Patent
View more database links
Registry Numbers Types Sources
261305 Beilstein Registry Number Beilstein
515-64-0 CAS Registry Number KEGG DRUG
515-64-0 CAS Registry Number NIST Chemistry WebBook
515-64-0 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
11431418 PubMed citation Europe PMC
13316533 PubMed citation Europe PMC
24727175 PubMed citation Europe PMC
621636 PubMed citation Europe PMC
6483571 PubMed citation Europe PMC
7051761 PubMed citation Europe PMC
Last Modified
22 February 2017