Chemical Component Summary | |
|---|---|
| Name | SULFANILAMIDE |
| Identifiers | 4-aminobenzenesulfonamide |
| Formula | C6 H8 N2 O2 S |
| Molecular Weight | 172.205 |
| Type | NON-POLYMER |
| Isomeric SMILES | c1cc(ccc1N)S(=O)(=O)N |
| InChI | InChI=1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10) |
| InChIKey | FDDDEECHVMSUSB-UHFFFAOYSA-N |
Chemical Details | |
|---|---|
| Formal Charge | 0 |
| Atom Count | 19 |
| Chiral Atom Count | 0 |
| Bond Count | 19 |
| Aromatic Bond Count | 6 |
Drug Info: DrugBank
| DrugBank ID | DB00259 |
|---|---|
| Name | Sulfanilamide |
| Groups | approved |
| Description | Sulfanilamide is a molecule containing the sulfonamide functional group attached to an aniline. |
| Synonyms |
|
| Brand Names |
|
| Indication | For the treatment of vulvovaginitis caused by <i>Candida albicans</i>. |
| Categories |
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| ATC-Code |
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| CAS number | 63-74-1 |
Drug Targets
| Name | Target Sequence | Pharmacological Action | Actions |
|---|---|---|---|
| Dihydropteroate synthase | MKLFAQGTSLDLSHPHVMGILNVTPDSFSDGGTHNSLIDAVKHANLMINA... | unknown | inhibitor |
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison
T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS.
Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682
Related Resource References
| Resource Name | Reference |
|---|---|
| Pharos | CHEMBL21 |
| PubChem | 5333, 129828936 |
| ChEMBL | CHEMBL21 |
| ChEBI | CHEBI:45373 |
| CCDC/CSD | SULAMD07, HUWHEO, SULAMD08, SULAMD10, BEYZEM, YORREC, SULAMD12, VOHKAG, SULAMD11, XIFNAC01, SANAPY, JEMVIG, SULAMD03, NUMHIO, STHSAM01, SULAMD06, ZILNEP, VIJYES, SULAMD04, UVATOD, SULAMD14, SULAMD13, QAJGIV |
| COD | 4516494, 1519191, 1519208, 1519207, 1519216, 1519228, 2016567, 1542815 |
