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55520-67-7

55520-67-7 Structure

55520-67-7 Structure
IdentificationBack Directory
[Name]

5-vinyl-2'-deoxyuridine
[CAS]

55520-67-7
[Synonyms]

5-Vinyl-dUrd
BrivudineImpurity10
5-vinyldeoxyuridine
5-vinyl-2'-deoxyuridine
2'-Deoxy-5-vinyluridine
2'-Deoxy-5-ethenyluridine
Uridine, 2'-deoxy-5-ethenyl-
5-Vinyl-2'-deoxyuridine (5-VdU)
5-VINYLDEOXYURIDINE; 2'-DEOXY-5-ETHENYLURIDINE; 5-VINYL-DURD; 2'-DEOXY-5-VINYLURIDINE
[Molecular Formula]

C11H14N2O5
[MDL Number]

MFCD01675693
[MOL File]

55520-67-7.mol
[Molecular Weight]

254.24
Chemical PropertiesBack Directory
[Melting point ]

106-110 °C (decomp)
[Boiling point ]

397.45°C (rough estimate)
[density ]

1.2983 (rough estimate)
[refractive index ]

1.5700 (estimate)
[solubility ]

soluble in DMSO
[form ]

Solid
[pka]

9.07±0.10(Predicted)
[Appearance]

yellowish solid
Hazard InformationBack Directory
[Description]

VdU (5-Vinyl-2’-deoxyuridine) is a synthetic analog of thymidine that can be used to study de novo DNA synthesis and cell proliferation. It is a potential replacement for BrdU (5-Bromo-2’-deoxyuridine) or EdU (5-Ethynyl-2’-deoxyuridine).


VdU incorporates into replicating DNA during the S-phase of the cell cycle instead of natural thymidine. The resulting vinyl-functionalized DNA can be detected by introducing either a biotin or fluorescent dye group via a cooper-free alkene-tetrazine reaction (also known as Inverse electron demand Diels-Alder ligation or IEDDA) and used for subsequent DNA purification or cell imaging tasks.

[Uses]

5-Vinyl-2'-deoxyuridine (5-VINYL-DURD), a thymidine analogue, is incorporated into cellular DNA during DNA replication. 5-Vinyl-2'-deoxyuridine is a click chemistry reagent, it contains an Alkyne group and induces DNA damage leads to apoptosis in human cultured cells[1].
[References]

[1] Yizhu Li, et al. DNA templated Click Chemistry via 5-vinyl-2'-deoxyuridine and an acridine-tetrazine conjugate induces DNA damage and apoptosis in cancer cells. Life Sci. 2023 Oct 1:330:122000. DOI:10.1016/j.lfs.2023.122000
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