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- Sulfanilamide abstract "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). 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: Furosemide, a loop diuretic Sulfadiazine, an antibiotic Sulfamethoxazole, an antibioticSulfanilamide was first prepared in 1908 by Paul Gelmo as part of his dissertation for a doctoral degree from the Technische Hochsschule of Vienna, Austria. It was patented in 1909.Gerhard Domagk, who directed the testing of the prodrug Prontosil in 1935, 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, are generally credited with the discovery of sulfanilamide as a chemotherapeutic agent. Domagk was awarded the Nobel Prize for his work.".
- Sulfanilamide atcPrefix "J01".
- Sulfanilamide atcSuffix "EB06".
- Sulfanilamide casNumber "63-74-1".
- Sulfanilamide chEBI "45373".
- Sulfanilamide drugbank "DB00259".
- Sulfanilamide fdaUniiCode "21240MF57M".
- Sulfanilamide iupacName "4-aminobenzenesulfonamide".
- Sulfanilamide pubchem "5333".
- Sulfanilamide thumbnail Sulfanilamide-skeletal.svg?width=300.
- Sulfanilamide wikiPageID "5642037".
- Sulfanilamide wikiPageRevisionID "586335066".
- Sulfanilamide atcPrefix "J01".
- Sulfanilamide atcSuffix "EB06".
- Sulfanilamide c "6".
- Sulfanilamide casNumber "63".
- Sulfanilamide chebi "45373".
- Sulfanilamide chembl "21".
- Sulfanilamide chemspiderid "5142".
- Sulfanilamide density "1.08".
- Sulfanilamide drugbank "DB00259".
- Sulfanilamide h "8".
- Sulfanilamide hasPhotoCollection Sulfanilamide.
- Sulfanilamide inchi "1".
- Sulfanilamide inchikey "FDDDEECHVMSUSB-UHFFFAOYAI".
- Sulfanilamide iupacName "4".
- Sulfanilamide kegg "D08543".
- Sulfanilamide meltingPoint "165".
- Sulfanilamide molecularWeight "172.2".
- Sulfanilamide n "2".
- Sulfanilamide niaidChemdb "19103".
- Sulfanilamide o "2".
- Sulfanilamide pubchem "5333".
- Sulfanilamide s "1".
- Sulfanilamide smiles "O=SN".
- Sulfanilamide stdinchi "1".
- Sulfanilamide stdinchikey "FDDDEECHVMSUSB-UHFFFAOYSA-N".
- Sulfanilamide unii "21240".
- Sulfanilamide verifiedrevid "470473303".
- Sulfanilamide subject Category:Sulfonamides.
- Sulfanilamide type Drug.
- Sulfanilamide type DrugProduct.
- Sulfanilamide type FunctionalSubstance.
- Sulfanilamide comment "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).".
- Sulfanilamide label "Sulfanilamid".
- Sulfanilamide label "Sulfanilamid".
- Sulfanilamide label "Sulfanilamida".
- Sulfanilamide label "Sulfanilamide".
- Sulfanilamide label "Sulfanilamide".
- Sulfanilamide label "Sulfanilamide".
- Sulfanilamide label "Sulfapreparaat".
- Sulfanilamide label "Сульфаниламид".
- Sulfanilamide sameAs Sulfanilamid.
- Sulfanilamide sameAs Sulfanilamide.
- Sulfanilamide sameAs Sulfanilamide.
- Sulfanilamide sameAs Sulfapreparaat.
- Sulfanilamide sameAs Sulfanilamid.
- Sulfanilamide sameAs Sulfanilamida.
- Sulfanilamide sameAs m.0dxv39.
- Sulfanilamide sameAs Q423423.
- Sulfanilamide sameAs Q423423.
- Sulfanilamide sameAs Sulfanilamide.
- Sulfanilamide sameAs DB00259.
- Sulfanilamide sameAs 5333.
- Sulfanilamide wasDerivedFrom Sulfanilamide?oldid=586335066.
- Sulfanilamide depiction Sulfanilamide-skeletal.svg.
- Sulfanilamide isPrimaryTopicOf Sulfanilamide.