D1413

2′,3′-Didehydro-3′-Desoxythymidin

≥98% (TLC)

• Synonym(e): 1-[(2R,5S)-5-(Hydroxymethyl)-2,5-dihydrofuran-2-yl]-5-methylpyrimidin-2,4-(1H,3H)-dion, Stavudine
• Empirische Formel (Hill-System): C₁₀H₁₂N₂O₄
• CAS-Nummer: 3056-17-5
• Molekulargewicht: 224.21
• NACRES: NA.77
• PubChem Substance ID: 24278356
• UNSPSC Code: 12352200
• MDL number: MFCD00132921
• Assay: ≥98% (TLC)
• Form: powder

Eigenschaften

• Quality Segment: 200
• assay: ≥98% (TLC)
• form: powder
• storage temp.: −20°C
• SMILES string: CC1=CN([C@@H]2O[C@H](CO)C=C2)C(=O)NC1=O
• InChI: 1S/C10H12N2O4/c1-6-4-12(10(15)11-9(6)14)8-3-2-7(5-13)16-8/h2-4,7-8,13H,5H2,1H3,(H,11,14,15)/t7-,8+/m0/s1
• InChI key: XNKLLVCARDGLGL-JGVFFNPUSA-N

Beschreibung

General description

2′,3′-Didehydro-3′-deoxythymidine (d4T), a pyrimidine analogue is the inhibitor of reverse transcriptase.

Application

2′,3′-Didehydro-3′-deoxythymidine has been used in cell treatment. It has also been used as a drug in Caenorhabditis elegans to study drug induced mitochondrial toxicity. It has also been used in the preclinical evaluation of GS-9160.

Biochem/physiol Actions

2′,3′-Didehydro-3′-deoxythymidine is a nucleoside analog, which inhibits HIV replication in vitro. Stavudine has the ability to enter the cells by non-facilitated diffusion. It possesses inhibitory activity against moloney murine leukemia virus, friend murine leukemia virus and simian immunodeficiency virus.[1]

Sicherheitshinweise

• Lagerklasse: 11 - Combustible Solids
• wgk: WGK 2
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)