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CAS 30771-43-8

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Uridine, 5-methoxy-2-thio-

Description:
Uridine, 5-methoxy-2-thio- (CAS 30771-43-8) is a modified nucleoside that features a uridine base with a methoxy group at the 5-position and a thio group at the 2-position of the ribose sugar. This compound is characterized by its ability to participate in various biochemical processes, particularly in nucleic acid metabolism. The presence of the methoxy group can influence its solubility and stability, while the thio modification may enhance its biological activity or alter its interaction with enzymes and receptors. Uridine derivatives are often studied for their potential therapeutic applications, including neuroprotective effects and roles in cellular signaling. The structural modifications in uridine can affect its pharmacokinetics and pharmacodynamics, making it a subject of interest in medicinal chemistry and biochemistry. Overall, Uridine, 5-methoxy-2-thio- represents a unique variant of nucleosides with potential implications in research and therapeutic development.
Formula:C10H14N2O6S
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Found 3 products.
  • Uridine, 5-methoxy-2-thio-

    CAS:
    Formula:C10H14N2O6S
    Molecular weight:290.293

    Ref: IN-DA00319K

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  • 5-Methoxy-2-thiouridine

    CAS:
    Nucleoside Derivatives - 5-Modified pyrimidine nucleosides, Thio-nucleosides
    Formula:C10H14N2O6S
    Color and Shape:Solid
    Molecular weight:290.29
  • 5-Methoxy-2-thiouridine

    CAS:
    <p>5-Methoxy-2-thiouridine is the peracylated form of thiouracil. It is a reactive oxygen species, which can cause primary site lesions in cells. 5-Methoxy-2-thiouridine is a posttranscriptional modification that leads to conformational changes in the anticodon loop of tRNA molecules. This modification prevents the anticodon from pairing with its corresponding codon during translation, thereby inhibiting protein synthesis. The modifications also affect RNA processing and stability and lead to changes in gene expression.</p>
    Purity:Min. 95%

    Ref: 3D-FM162894

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