Edoxudine

CAS No. 15176-29-1

Edoxudine( Edoxudine | CCRIS 2349 | CCRIS2349 | Edoxudina )

Catalog No. M18060 CAS No. 15176-29-1

Edoxudine, an antiviral drug, is an analogue of thymidine and shows effectiveness against the herpes simplex virus.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 41 In Stock
25MG 70 In Stock
50MG 104 In Stock
100MG 177 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Edoxudine
  • Note
    Research use only, not for human use.
  • Brief Description
    Edoxudine, an antiviral drug, is an analogue of thymidine and shows effectiveness against the herpes simplex virus.
  • Description
    Edoxudine, an antiviral drug, is an analogue of thymidine and shows effectiveness against the herpes simplex virus. Edoxudine is used as a 5-fluorouracil (FU) modulator. Edoxudine may be used to enhance the therapeutic index of 5-FU by reducing the catabolism, prolonging the plasma and intratumoral concentrations of 5-FU, and offering protection to normal organs by increasing the endogenous uridine levels. It can also enhance the antitumour action of 5-FU.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Edoxudine | CCRIS 2349 | CCRIS2349 | Edoxudina
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    PPAR
  • Recptor
    Antiviral
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    15176-29-1
  • Formula Weight
    256.26
  • Molecular Formula
    C11H16N2O5
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 125 mg/mL; 487.79 mM
  • SMILES
    CCc1cn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]c1=O
  • Chemical Name
    5-Ethyldeoxyuridine

Shipping & Storage Information

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

Reference

1. Kralovanszky, et al. 5-Ethyl-2'-deoxyuridine, a modulator of both antitumour action and pharmacokinetics of 5-fluorouracil[J]. Journal of Cancer Research & Clinical Oncology, 1999, 125(12):675-684.
molnova catalog
related products
  • Hydroxyfasudil Hydro...

    Hydroxyfasudil hydrochloride is a ROCK1/2 inhibitor (IC50s: 0.73/0.72 μM).

  • JW55

    JW 55 is an inhibitor of the PARP domain of tankyrase 1 and 2 (TNKS1/2). JW55 decreased auto-PARsylation of TNKS1/2 in vitro with IC50 values of 1.9 uM and 830 nM respectively.

  • Saroglitazar

    A novel PPAR agonist with predominant PPARα and moderate PPARγ activity with EC50 of 0.65 pM and 3 nM respectively.