Stavudine

CAS No. 3056-17-5

Stavudine( d4T | NSC 163661 )

Catalog No. M13973 CAS No. 3056-17-5

Stavudine is a nucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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200MG 59 In Stock
500MG 87 In Stock
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Biological Information

  • Product Name
    Stavudine
  • Note
    Research use only, not for human use.
  • Brief Description
    Stavudine is a nucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV.
  • Description
    Stavudine is a nucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV.(In Vitro):Stavudine (d4T) (50 μM) significantly reduces the expression of the NLRP3 inflammasome gene, IL-18 production and Aβ 42-stimulated cellular production of IL-1β in THP-1 derived macrophages.Stavudine (d4T) (50 μM) inhibits the assembly of the NLRP3 inflammasome complex and down-regulates the phagocytosis of Aβ 42 by macrophages.Stavudine (d4T) (10 μM, 7 or 14 days) significantly induced CEM cells apoptosis, especially after 14 days, and increases hydrogen peroxide levels.(In Vivo):Stavudine (d4T) (500 mg/kg, daily liquid, 2 weeks) can rapidly induce fat depletion and mild liver damage at high dose in male RjOrl Swiss mice.
  • In Vitro
    Stavudine (d4T) (50 μM) significantly reduces the expression of the NLRP3 inflammasome gene, IL-18 production and Aβ 42-stimulated cellular production of IL-1β in THP-1 derived macrophages.Stavudine (d4T) (50 μM) inhibits the assembly of the NLRP3 inflammasome complex and down-regulates the phagocytosis of Aβ 42 by macrophages.Stavudine (d4T) (10 μM, 7 or 14 days) significantly induced CEM cells apoptosis, especially after 14 days, and increases hydrogen peroxide levels.
  • In Vivo
    Stavudine (d4T) (500 mg/kg, daily liquid, 2 weeks) can rapidly induce fat depletion and mild liver damage at high dose in male RjOrl Swiss mice. Animal Model:Male RjOrl Swiss mice weighing 0.028-0.03 kg Dosage:500 mg/kg Administration:Daily liquid; 2 weeks Result:Reduced fat weight gain by 58%, 5.7 g in the control group and 4.9 g in the d4T treated group.Significantly elevated plasma ALT and LDH levels.Reduced plasma acetoacetic acid and beta-hydroxybutyric acid levels.Reduced liver and muscle mtDNA levels at high dose concentration of 500 mg/kg.
  • Synonyms
    d4T | NSC 163661
  • Pathway
    Microbiology/Virology
  • Target
    Reverse Transcriptase
  • Recptor
    Reverse Transcriptase
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    3056-17-5
  • Formula Weight
    224.21
  • Molecular Formula
    C10H12N2O4
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 15 mg/mL (66.9 mM); DMSO: 45 mg/mL (200.7 mM)
  • SMILES
    OC[C@@H]1C=C[C@H](N2C(NC(C(C)=C2)=O)=O)O1
  • Chemical Name
    1-((2R,5S)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Lea AP, Faulds D. Drugs. 1996 May;51(5):846-64.
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