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Chemical Structure
Chemical Structure
Chemical Structure

Clevudine [163252-36-6]

Research Use Only
AG-CR1-3736
AdipoGen Life Sciences
CAS Number163252-36-6
Product group Chemicals
Estimated Purity>98%
Molecular Weight260.2
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Packing Size
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    Clevudine [163252-36-6]
  • Delivery Days Customer
    10
  • CAS Number
    163252-36-6
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Molecular Formula
    C10H13FN2O5
  • Molecular Weight
    260.2
  • Scientific Description
    Chemical. CAS: 163252-36-6. Formula: C10H13FN2O5. MW: 260.2. Clevudine is a synthetic pyrimidine nucleoside analog antiviral agent with activity against hepatitis B virus (HBV) and Epstein-Barr virus (EBV). Intracellularly, clevudine is phosphorylated to its active metabolites, clevudine monophosphate and triphosphate. The triphosphate metabolite competes with thymidine for incorporation into viral DNA, thereby causing DNA chain termination and inhibiting the function of HBV DNA polymerase and reverse transcriptase, consequently blocking the viral replication. It also blocks the DNA supply of the virus into the nucleus, reducing the amount of cccDNA by 20-100 times. Potentially useful for the treatment of the SARS-CoV-2 (COVID-19) infection, acting as a potent inhibitor of the RdRp protein. - Clevudine is a synthetic pyrimidine nucleoside analog antiviral agent with activity against hepatitis B virus (HBV) and Epstein-Barr virus (EBV). Intracellularly, clevudine is phosphorylated to its active metabolites, clevudine monophosphate and triphosphate. The triphosphate metabolite competes with thymidine for incorporation into viral DNA, thereby causing DNA chain termination and inhibiting the function of HBV DNA polymerase and reverse transcriptase, consequently blocking the viral replication. It also blocks the DNA supply of the virus into the nucleus, reducing the amount of cccDNA by 20-100 times. Potentially useful for the treatment of the SARS-CoV-2 (COVID-19) infection, acting as a potent inhibitor of the RdRp protein.
  • SMILES
    O[C@H]1[C@H](CO)O[C@]([H])(N2C=C(C)C(NC2=O)=O)[C@@H]1F
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352200