Festinavir
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| Systematic (IUPAC) name | |
|---|---|
| 1-[(2R,5R)-5-ethynyl-5-(hydroxymethyl)-2H-furan-2-yl]-5-methylpyrimidine-2,4-dione | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | Investigational |
| Identifiers | |
| ATC code | None |
| PubChem | CID 3008897 |
| ChemSpider | 2278330 |
| ChEMBL | CHEMBL124363 |
| NIAID ChemDB | 209894 |
| Synonyms | 4'-ethynylstavudine |
| Chemical data | |
| Formula | C12H12N2O4 |
| Mol. mass | 248.235 g/mol |
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Festinavir is an investigational new drug being developed by Bristol Myers-Squibb for the treatment of HIV infection. Festinavir is a nucleoside reverse transcriptase inhibitor that is active against HIV resistant to both abacavir and tenofovir, making the drug a candidate for people with multi-drug resistant (MDR) strains of the virus. Festinavir is a derivative of stavudine (d4T), but is less toxic.[citation needed] It was originally developed at Yale University.[1]
References [edit]
- ^ Alcorn, Keith (21 December 2010). "Bristol-Myers Squibb buys festinavir, new NRTI active against MDR HIV". aidsmap.com. aidsmap. Retrieved 24 June 2011.
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