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Submit ReviewStavudine is a nucleoside analog; antiviral that inhibits HIV replication in vitro. Orally bioavailable.
Stavudine is also offered as part of the Tocriscreen FDA-Approved Drugs. Find out more about compound libraries available from Tocris.
M. Wt | 224.21 |
Formula | C10H12N2O4 |
Storage | Store at -20°C |
Purity | ≥99% (HPLC) |
CAS Number | 3056-17-5 |
PubChem ID | 18283 |
InChI Key | XNKLLVCARDGLGL-JGVFFNPUSA-N |
Smiles | [H]C1=C([H])[C@@H](O[C@@H]1CO)N1C=C(C)C(=O)NC1=O |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
References are publications that support the biological activity of the product.
Baba et al (1987) Both 2',3'-dideoxythymidine and its 2',3'-unsaturated derivative (2',3'-dideoxythymidinene) are potent and selective inhibitors of human immunodeficiency virus replication in vitro. Biochem.Biophys.Res.Commun. 142 128 PMID: 3028398
Riddler et al (1995) Antiretroviral activity of stav. (2',3'-didehydro-3'-deoxythymidine, D4T). Antiviral Res. 27 189 PMID: 8540743
Keywords: Stavudine, Stavudine supplier, Nucleoside, analogues, inhibits, HIV, replication, antiviral, 2,3-Didehydro-3-deoxythymidine, DNA,, RNA, and, Protein, Synthesis, 4990, Tocris Bioscience
Citations are publications that use Tocris products.
Currently there are no citations for Stavudine.
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Stavudine triphosphate was studied to understand how it affects cellular synthesis of mitochondrial DNA.
Cells were grown and differentiated, as described in the text, in the presence of 0, 1, or 10 μM AZT.