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CAS 78635-98-0

:

Thymidine, 3'-(4-oxopentanoate)

Description:
Thymidine, 3'-(4-oxopentanoate), with the CAS number 78635-98-0, is a derivative of thymidine, a nucleoside that plays a crucial role in DNA synthesis. This compound features a 4-oxopentanoate moiety attached to the 3' position of the thymidine molecule, which can influence its biochemical properties and interactions. Thymidine itself consists of a thymine base linked to a deoxyribose sugar, and the modification at the 3' position can affect its solubility, stability, and reactivity. Such derivatives are often studied for their potential applications in biochemistry and molecular biology, particularly in the context of nucleic acid research and drug development. The presence of the 4-oxopentanoate group may also impart unique characteristics, such as altered binding affinities or enhanced cellular uptake. Overall, this compound exemplifies the diverse modifications that can be made to nucleosides to explore their functional properties in various biological systems.
Formula:C15H20N2O7
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Found 2 products.
  • 3'-O-Levulinoyl-N-benzoyl-2'-deoxythymidine
    TRC
    + Info

    3'-O-Levulinoyl-N-benzoyl-2'-deoxythymidine

    Controlled Product
    CAS:
    <p>Applications 3'-O-Levulinoyl-N-benzoyl-2'-deoxythymidine is a protected nucleotide derivative/building block.<br>References Kiuru, E., et al.: Helvetica Chimica Acta, 96, 1997-2008 (2013);<br></p>
    Formula:C15H20N2O7
    Color and Shape:Neat
    Molecular weight:340.329

    Ref: TR-L379705

    500mg
    1,530.00€
  • 2'-Deoxy-3'-O-levulinoylthymidine
    Biosynth
    + Info

    2'-Deoxy-3'-O-levulinoylthymidine

    CAS:
    <p>2'-Deoxy-3'-O-levulinoylthymidine is a novel antiviral agent and a synthetic deoxyribonucleoside that is structurally similar to thymidine. It has been studied in vitro and in vivo for its antiviral activity against various viruses, including HIV type 1, HIV type 2, herpes simplex virus (HSV), varicella zoster virus (VZV), cytomegalovirus (CMV), and influenza A virus. 2'-Deoxy-3'-O-levulinoylthymidine has also shown anticancer properties in vitro. This drug inhibits the synthesis of DNA by competing with other nucleotides for incorporation into DNA during the elongation phase of replication. It also inhibits the synthesis of RNA by competing with other nucleotides for incorporation into RNA during transcription.</p>
    Formula:C15H20N2O7
    Purity:Min. 95%
    Molecular weight:340.33 g/mol

    Ref: 3D-ND16367

    1g
    303.00€
    2g
    449.00€
    5g
    997.00€
    10g
    1,816.00€