Page last updated: 2024-09-26

5-vinyl-2'-deoxyuridine

Description

5-vinyl-2'-deoxyuridine: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID148744
CHEMBL ID221928
SCHEMBL ID99491
MeSH IDM0057637

Synonyms (24)

Synonym
1-((2r,4s,5r)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-vinyl-1-h-pyrimidine-2,4-dione
5-vinyl-durd
1-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-5-vinyl-pyrimidine-2,4-dione
5-vinyl-2'-deoxyuridine
2'-deoxy-5-ethenyluridine
2'-deoxy-5-vinyluridine
brn 0755095
5-vinyl-deoxyuridine
uridine, 2'-deoxy-5-vinyl-
CHEMBL221928
5-ethenyl-1-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione
unii-87v72at994
87v72at994 ,
55520-67-7
SCHEMBL99491
5-vinyldeoxyuridine
uridine, 2'-deoxy-5-ethenyl-
DTXSID10970866
1-(2-deoxypentofuranosyl)-5-ethenyl-4-hydroxypyrimidin-2(1h)-one
Q27269846
1-((2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-vinylpyrimidine-2,4(1h,3h)-dione
A901366
vdu (5-vinyl-2'-deoxyuridine)
CS-0254681

Bioassays (3)

Assay IDTitleYearJournalArticle
AID85559Concentration required to reduce the number of viral plaques in vivo cell monolayers of herpes simplex virus type 1.1989Journal of medicinal chemistry, Feb, Volume: 32, Issue:2
Synthesis and antiviral activity of phosphonoacetic and phosphonoformic acid esters of 5-bromo-2'-deoxyuridine and related pyrimidine nucleosides and acyclonucleosides.
AID280941Cytotoxicity against mouse L1210/0 cells after 48 hrs2007Journal of medicinal chemistry, Apr-05, Volume: 50, Issue:7
Probing the anticancer activity of nucleoside analogues: a QSAR model approach using an internally consistent training set.
AID84605Concentration required to reduce the number of viral plaques in vivo cell monolayers of herpes simplex virus type 2.1989Journal of medicinal chemistry, Feb, Volume: 32, Issue:2
Synthesis and antiviral activity of phosphonoacetic and phosphonoformic acid esters of 5-bromo-2'-deoxyuridine and related pyrimidine nucleosides and acyclonucleosides.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (13)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (46.15)18.7374
1990's1 (7.69)18.2507
2000's2 (15.38)29.6817
2010's3 (23.08)24.3611
2020's1 (7.69)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (7.69%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other12 (92.31%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research Highlights

Pharmacokinetics (1)

ArticleYear
Single ascending dose tolerability, pharmacokinetic-pharmacodynamic study of dihydropyrimidine dehydrogenase inhibitor Ro 09-4889.
Clinical cancer research : an official journal of the American Association for Cancer Research, Apr-01, Volume: 10, Issue: 7
2004
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Dosage (1)

ArticleYear
Single ascending dose tolerability, pharmacokinetic-pharmacodynamic study of dihydropyrimidine dehydrogenase inhibitor Ro 09-4889.
Clinical cancer research : an official journal of the American Association for Cancer Research, Apr-01, Volume: 10, Issue: 7
2004
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]