Date published: 2025-12-18

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3′-Deoxyuridine (CAS 7057-27-4)

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Alternate Names:
3′-Deoxy Uridine
Application:
3′-Deoxyuridine is a potential anti-cancer and anti-viral agent
CAS Number:
7057-27-4
Molecular Weight:
228.20
Molecular Formula:
C9H12N2O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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3′-Deoxyuridine, a nucleoside derivative, has garnered significant interest in biochemical and molecular biology research due to its role in nucleic acid metabolism and DNA synthesis. This compound functions as a precursor in the synthesis of nucleic acids, serving as a substrate for DNA polymerases during DNA replication and repair processes. Research has explaind its mechanism of action, highlighting its involvement in the biosynthesis of DNA and its potential as a modulator of DNA synthesis pathways. Additionally, 3′-Deoxyuridine has been utilized in studies investigating DNA damage and repair mechanisms, providing insights into the cellular responses to genotoxic stress and DNA lesions. Moreover, it serves as a valuable tool in the development of nucleoside analogs for antiviral and anticancer research, with researchers exploring its structural modifications to enhance its efficacy and selectivity against viral and cancerous cells. Furthermore, this chemical compound finds applications in molecular biology techniques such as PCR (Polymerase Chain Reaction) and nucleic acid labeling, facilitating the amplification and detection of specific DNA sequences in research laboratories. Overall, 3′-Deoxyuridine plays a crucial role in advancing our understanding of nucleic acid biochemistry and molecular biology, offering valuable insights into DNA synthesis, repair, and manipulation.


3′-Deoxyuridine (CAS 7057-27-4) References

  1. Inhibition of the replication of a hepatitis C virus-like RNA template by interferon and 3'-deoxycytidine.  |  King, RW., et al. 2002. Antivir Chem Chemother. 13: 363-70. PMID: 12718408
  2. The regiospecific one-pot phosphorylation of either the 5'- or 2'-hydroxyl in 3'-deoxycytidines without protection: critical role of the base.  |  Howes, PD., et al. 2003. Nucleosides Nucleotides Nucleic Acids. 22: 687-9. PMID: 14565254
  3. Synthesis of beta-enantiomers of N4-hydroxy-3'-deoxypyrimidine nucleosides and their evaluation against bovine viral diarrhoea virus and hepatitis C virus in cell culture.  |  Hollecker, L., et al. 2004. Antivir Chem Chemother. 15: 43-55. PMID: 15074714
  4. Pac13 is a Small, Monomeric Dehydratase that Mediates the Formation of the 3'-Deoxy Nucleoside of Pacidamycins.  |  Michailidou, F., et al. 2017. Angew Chem Int Ed Engl. 56: 12492-12497. PMID: 28786545
  5. Expanding structural diversity of 5'-aminouridine moiety of sansanmycin via mutational biosynthesis.  |  Lu, Y., et al. 2023. Front Bioeng Biotechnol. 11: 1278601. PMID: 38026887
  6. Synthetic nucleosides and nucleotides. XXXV. Synthesis and biological evaluations of 5-fluoropyrimidine nucleosides and nucleotides of 3-deoxy-beta-D-ribofuranose and related compounds.  |  Saneyoshi, M., et al. 1995. Chem Pharm Bull (Tokyo). 43: 2005-9. PMID: 8575037

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3′-Deoxyuridine, 25 mg

sc-220905
25 mg
$390.00

3′-Deoxyuridine, 50 mg

sc-220905A
50 mg
$500.00

3′-Deoxyuridine, 100 mg

sc-220905B
100 mg
$930.00

3′-Deoxyuridine, 250 mg

sc-220905C
250 mg
$1575.00

3′-Deoxyuridine, 500 mg

sc-220905D
500 mg
$2000.00

3′-Deoxyuridine, 1 g

sc-220905E
1 g
$3000.00