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Chemical Structure
Chemical Structure
Chemical Structure

Ganciclovir [82410-32-0]

Research Use Only
CDX-G0046
Chemodex
CAS Number82410-32-0
Product group Chemicals
Estimated Purity>99%
Molecular Weight255.23
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Ganciclovir [82410-32-0]
  • Delivery Days Customer
    10
  • CAS Number
    82410-32-0
  • Certification
    Research Use Only
  • Estimated Purity
    >99%
  • Hazard Information
    Danger
  • Molecular Formula
    C9H13N5O4
  • Molecular Weight
    255.23
  • Scientific Description
    Chemical. CAS: 82410-32-0. Formula: C9H13N5O4. MW: 255.23. Ganciclovir is antiviral synthetic analog of the nucleoside 2-deoxy-guanosine, which is used to treat or prevent cytomegalovirus (CMV) infections. It acts as a prodrug activated by phosphorylation. It is first phosphorylated to ganciclovir monophosphate by a viral kinase encoded by the cytomegalovirus (CMV) gene UL97 during infection. Subsequently, cellular kinases catalyze the formation of ganciclovir diphosphate and ganciclovir triphosphate. Ganciclovir triphosphate is a competitive inhibitor of deoxyguanosine triphosphate (dGTP) incorporation into DNA and preferentially inhibits viral DNA polymerases more than cellular DNA polymerases. It is also useful in the study of gene therapy in cancer research. Ganciclovir has been used in the study of suicide gene therapy in cancer research, where upon expression of a viral suicide gene encoding herpes simplex virus, thymidine kinase (TK), the non-toxic prodrug ganciclovir, is converted to an active phosphorylated analog that can be incorporated into the DNA of replicating eukaryotic cells, causing death of the malignant dividing cell. Causes an irreversible cell cycle arrest at the G2/M checkpoint. Ganciclovir has also been used to study the loss of telomeres and to evaluate sensitivity of viruses to antiviral agents. - Ganciclovir is antiviral synthetic analog of the nucleoside 2-deoxy-guanosine, which is used to treat or prevent cytomegalovirus (CMV) infections. It acts as a prodrug activated by phosphorylation. It is first phosphorylated to ganciclovir monophosphate by a viral kinase encoded by the cytomegalovirus (CMV) gene UL97 during infection. Subsequently, cellular kinases catalyze the formation of ganciclovir diphosphate and ganciclovir triphosphate. Ganciclovir triphosphate is a competitive inhibitor of deoxyguanosine triphosphate (dGTP) incorporation into DNA and preferentially inhibits viral DNA polymerases more than cellular DNA polymerases. It is also useful in the study of gene therapy in cancer research. Ganciclovir has been used in the study of suicide gene therapy in cancer research, where upon expression of a viral suicide gene encoding herpes simplex virus, thymidine kinase (TK), the non-toxic prodrug ganciclovir, is converted to an active phosphorylated analog that can be incorporated into the DNA of replicating eukaryotic cells, causing death of the malignant dividing cell. Causes an irreversible cell cycle arrest at the G2/M checkpoint. Ganciclovir has also been used to study the loss of telomeres and to evaluate sensitivity of viruses to antiviral agents.
  • SMILES
    O=C1C2=C(N(COC(CO)CO)C=N2)N=C(N)N1
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352200