Tegafur
| Clinical data | |
|---|---|
| Other names | 5-fluoro-1-(oxolan-2-yl)pyrimidine-2,4-dione | 
| AHFS/Drugs.com | International Drug Names | 
| License data | |
| Pregnancy category | 
 | 
| Routes of administration | Oral | 
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Elimination half-life | 3.9-11 hours | 
| Identifiers | |
| 
 | |
| CAS Number | |
| PubChem CID | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.038.027 | 
| Chemical and physical data | |
| Formula | C8H9FN2O3 | 
| Molar mass | 200.169 g·mol−1 | 
| 3D model (JSmol) | |
| 
 | |
| 
 | |
| (what is this?) (verify) | |
Tegafur is a chemotherapeutic prodrug of 5-fluorouracil (5-FU) used in the treatment of cancers. It is a component of the combination drug tegafur/uracil. When metabolised, it becomes 5-FU.
It was patented in 1967 and approved for medical use in 1972.