This articleneeds additional citations forverification. Please helpimprove this article byadding citations to reliable sources. Unsourced material may be challenged and removed. Find sources: "Sulfafurazole" – news ·newspapers ·books ·scholar ·JSTOR(August 2014) (Learn how and when to remove this message) |
| Clinical data | |
|---|---|
| AHFS/Drugs.com | International Drug Names |
| MedlinePlus | a601049 |
| Pregnancy category |
|
| Routes of administration | Oral |
| ATC code | |
| Legal status | |
| Legal status |
|
| Pharmacokinetic data | |
| Excretion | Excreted unchanged in urine |
| Identifiers | |
| |
| CAS Number |
|
| PubChemCID | |
| DrugBank |
|
| ChemSpider | |
| UNII | |
| KEGG |
|
| ChEMBL | |
| CompTox Dashboard(EPA) | |
| ECHA InfoCard | 100.004.418 |
| Chemical and physical data | |
| Formula | C11H13N3O3S |
| Molar mass | 267.30 g·mol−1 |
| 3D model (JSmol) | |
| Melting point | 194 °C (381 °F) |
| |
| |
| | |
Sulfafurazole (INN, also known assulfisoxazole) is asulfonamideantibacterial with a dimethyl-isoxazole substituent. It possessesantibiotic activity against a wide range ofGram-negative andGram-positive organisms.[1] It is sometimes given in combination witherythromycin (seeerythromycin/sulfafurazole) orphenazopyridine. It is used locally in a 4% solution orointment.
This systemicantibiotic-related article is astub. You can help Wikipedia byexpanding it. |