Didanosine

CAS No. 69655-05-6

Didanosine ( NSC 612049 )

Catalog No. M15668 CAS No. 69655-05-6

Didanosine is a reverse transcriptase inhibitor with an IC50 of 0.49 μM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 31 In Stock
10MG 50 In Stock
25MG 77 In Stock
50MG 102 In Stock
100MG 151 In Stock
200MG 224 In Stock
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Biological Information

  • Product Name
    Didanosine
  • Note
    Research use only, not for human use.
  • Brief Description
    Didanosine is a reverse transcriptase inhibitor with an IC50 of 0.49 μM.
  • Description
    Didanosine is a reverse transcriptase inhibitor with an IC50 of 0.49 μM.(In Vitro):Didanosine is converted by cellular enzymes to the active antiviral metabolite dideoxyadenosine triphosphate (dd-ATP) and the intracellular half life of dd-ATP varies from 8-24 hours.Didanosine shows antiretroviral activity with IC50 value of 0.24-0.6 mg/L for HIV infection.Didanosine (5, 10, 50, 100 ug/ml; 24, 48 h) shows no significant inhibition of cell proliferation in IEC-6 cells.(In Vivo):Didanosine (100, 150 mg/kg; p.o.; daily for 7 days) decreases the length of duodenal and in jejunal villus in mouse.
  • In Vitro
    Didanosine is converted by cellular enzymes to the active antiviral metabolite dideoxyadenosine triphosphate (dd-ATP) and the intracellular half life of dd-ATP varies from 8-24 hours.Didanosine shows antiretroviral activity with IC50 value of 0.24-0.6 mg/L for HIV infection.Didanosine (5, 10, 50, 100 ug/ml; 24, 48 h) shows no significant inhibition of cell proliferation in IEC-6 cells. Cell Proliferation Assay Cell Line:IEC-6 cells Concentration:5, 10, 50, 100 ug/ml Incubation Time:24, 48 h Result:Did not show any significant inhibition of cell proliferation at either 24 h or 48 h.Apoptosis Analysis Cell Line:IEC-6 cells Concentration:100 ug/ml Incubation Time:24 h Result:Induced apoptosis with the apoptosis rates of 4.7% to 7.4%.
  • In Vivo
    Didanosine (100, 150 mg/kg; p.o.; daily for 7 days) decreases the length of duodenal and in jejunal villus in mouse. Animal Model:30-40 g, male swiss mice Dosage:100, 150 mg/kg Administration:P.o.; daily for 7 days Result:Caused significant reductions in duodenal and in jejunal villus length and significantly decreased ileal crypt depth.
  • Synonyms
    NSC 612049
  • Pathway
    Microbiology/Virology
  • Target
    Reverse Transcriptase
  • Recptor
    Reverse Transcriptase
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    69655-05-6
  • Formula Weight
    236.23
  • Molecular Formula
    C10H12N4O3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 47 mg/mL (198.95 mM)
  • SMILES
    C1C[C@@H](O[C@@H]1CO)N2C=NC3=C2NC=NC3=O
  • Chemical Name
    9-[(2R,5S)-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one

Shipping & Storage Information

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

Reference

1.Benbrik E, et al. J Neurol Sci, 1997, 149(1), 19-25.
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