5-vinyl-2'-deoxyuridine: structure
ID Source | ID |
---|---|
PubMed CID | 148744 |
CHEMBL ID | 221928 |
SCHEMBL ID | 99491 |
MeSH ID | M0057637 |
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 |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID85559 | Concentration required to reduce the number of viral plaques in vivo cell monolayers of herpes simplex virus type 1. | 1989 | Journal 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. |
AID280941 | Cytotoxicity against mouse L1210/0 cells after 48 hrs | 2007 | Journal 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. |
AID84605 | Concentration required to reduce the number of viral plaques in vivo cell monolayers of herpes simplex virus type 2. | 1989 | Journal 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] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 6 (46.15) | 18.7374 |
1990's | 1 (7.69) | 18.2507 |
2000's | 2 (15.38) | 29.6817 |
2010's | 3 (23.08) | 24.3611 |
2020's | 1 (7.69) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 1 (7.69%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 12 (92.31%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Article | Year |
---|---|
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] |
Article | Year |
---|---|
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] |