3'-Deoxy-3'-fluorothymidine

CAS No. 25526-93-6

3'-Deoxy-3'-fluorothymidine( MIV-310 | CL-184824 | MIV310 )

Catalog No. M19362 CAS No. 25526-93-6

An antiviral agent.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 30 In Stock
25MG 58 In Stock
50MG 91 In Stock
100MG 121 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    3'-Deoxy-3'-fluorothymidine
  • Note
    Research use only, not for human use.
  • Brief Description
    An antiviral agent.
  • Description
    Alovudine is a reverse transcriptase inhibitor potentially for the treatment of HIV infection. A 4-week randomized, double-blind, placebo-controlled dose-ranging study concluded that alovudine 2 mg/day provided a modest but significant viral load reduction in patients harbouring viruses.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    MIV-310 | CL-184824 | MIV310
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Antiviral
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    25526-93-6
  • Formula Weight
    244.22
  • Molecular Formula
    C10H13FN2O4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (409.47 mM)
  • SMILES
    CC1=CN(C(=O)NC1=O)[C@H]2C[C@H](F)[C@@H](CO)O2
  • Chemical Name
    3'-Deoxy-3'-fluorothymidine

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • 11beta,13-Dihydrolac...

    11,13-Dihydrolactucin is a useful organic compound for research related to life sciences.

  • P-gb-IN-1

    P-gb-IN-1 is a potent P-glycoprotein (P-gp) inhibitor that exhibits reverse activity by inhibiting P-gp outflow. P-gb-IN-1 has been shown to inhibit P-gp by hydrogen bonding with residues Asn 721 and Met 986. P-gb-IN-1 showed low toxicity in MCF-7/ADR cells.

  • 1H-1-ethyl Candesart...

    1H-1-ethyl Candesartan Cilexetil is a process-related impurity in the bulk synthesis of candesartan cilexetil, which is a potent, long-acting and selective angiotensin II type 1 receptor (AT1) antagonist.