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Systematic (IUPAC) name | |
4-aminobenzenesulfonamide | |
Clinical data | |
AHFS/Drugs.com | Consumer Drug Information |
Pregnancy cat. | ? |
Legal status | ? |
Identifiers | |
CAS number | 63-74-1 ![]() |
ATC code | J01EB06 D06BA05 QJ01EQ06 |
PubChem | CID 5333 |
DrugBank | DB00259 |
ChemSpider | 5142 ![]() |
UNII | 21240MF57M ![]() |
KEGG | D08543 ![]() |
ChEBI | CHEBI:45373 ![]() |
ChEMBL | CHEMBL21 ![]() |
NIAID ChemDB | 019103 |
Chemical data | |
Formula | C6H8N2O2S |
Mol. mass | 172.20 g/mol |
SMILES | eMolecules & PubChem |
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Physical data | |
Density | 1.08 g/cm³ |
Melt. point | 165 °C (329 °F) |
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Sulfanilamide (also spelled sulphanilamide) is a sulfonamide antibacterial. Chemically, it is a molecule containing the sulfonamide functional group attached to an aniline. As a sulfonamide antibiotic, it functions by competitively inhibiting (i.e., by acting as a substrate analogue) enzymatic reactions involving para-aminobenzoic acid (PABA).[1] PABA is needed in enzymatic reactions that produce folic acid which acts as a coenzyme in the synthesis of purine, pyrimidine and other amino acids.
The term "sulfanilamides" is also used to describe a family of molecules containing these functional groups. Examples include:
Gerhard Domagk, who directed the testing of the prodrug Prontosil in 1935,[2] and Jacques and Thérèse Tréfouël, who along with Federico Nitti and Daniel Bovet in the laboratory of Ernest Fourneau at the Pasteur Institute, determined sulfanilamide as the active form,[3] are generally credited with the discovery of sulfanilamide as a chemotherapeutic agent. Domagk was awarded the Nobel Prize for his work.[4]
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