Bexarotene
| Clinical data | |
|---|---|
| Trade names | Targretin |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a608006 |
| License data |
|
| Routes of administration | By mouth, topical |
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Protein binding | >99% |
| Metabolism | Hepatic (CYP3A4-mediated) |
| Elimination half-life | 7 hours |
| Excretion | Parent drug and metabolites are eliminated primarily through the hepatobiliary system. Less than 1% is excreted in the urine unchanged. |
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| IUPHAR/BPS | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| ChEBI | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.206.790 |
| Chemical and physical data | |
| Formula | C24H28O2 |
| Molar mass | 348.486 g·mol−1 |
| 3D model (JSmol) | |
| |
| |
| (verify) | |
Bexarotene, sold under the brand Targretin, is an antineoplastic (anti-cancer) agent used for the treatment of cutaneous T cell lymphoma (CTCL). It is a third-generation retinoid.
It was approved by the U.S. Food and Drug Administration (FDA) in December 1999, and the European Medicines Agency (EMA) in March 2001. It is available as a generic medication.