Page last updated: 2024-12-06

3-oxauracil

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

3-Oxauracil, also known as uracil-6-one, is a heterocyclic compound related to uracil. It is a derivative of uracil with an additional carbonyl group at the 3-position. 3-Oxauracil has been studied for its potential biological activities, including its effects on DNA synthesis and its role in the formation of certain types of cancer. Its synthesis involves a multi-step process, and its effects are typically investigated in cell culture or animal models. Further research is needed to fully understand the role of 3-oxauracil in biological systems.'

3-oxauracil: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID73278
CHEMBL ID3250627
SCHEMBL ID288527
MeSH IDM0064635

Synonyms (25)

Synonym
3h-[1,3]oxazine-2,6-dione
2h-1,3-oxazine-2,6(3h)-dione
3h-1,3-oxazine-2,6-dione
nsc 163038
brn 0112222
1,3-oxazine-2,6-dione
2,3-dihydro-1,3-6h-oxazine-2,6-dione
nsc163038
3-oxauracil
2h-1,6(3h)-dione
34314-63-1
nsc-163038
AKOS004903244
unii-14lw71vvm6
14lw71vvm6 ,
2-27-00-00295 (beilstein handbook reference)
CHEMBL3250627
WQAIPNTUCFSZRZ-UHFFFAOYSA-N
SCHEMBL288527
DTXSID30187878
oxy-6h-1,3-oxazin-6-one
A912662
FT-0725220
2,3-dihydro-6h-1,3-oxazine-2,6-dione
CS-0359236
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID1136852Growth inhibition of mouse L1210 cells1979Journal of medicinal chemistry, May, Volume: 22, Issue:5
Synthesis and biological activity of 5-fluoro- and 5-methyl-1,3-oxazine-2,6(3H)-dione.
AID1136850Growth inhibition of Streptococcus faecium1979Journal of medicinal chemistry, May, Volume: 22, Issue:5
Synthesis and biological activity of 5-fluoro- and 5-methyl-1,3-oxazine-2,6(3H)-dione.
AID1136851Growth inhibition of Escherichia coli1979Journal of medicinal chemistry, May, Volume: 22, Issue:5
Synthesis and biological activity of 5-fluoro- and 5-methyl-1,3-oxazine-2,6(3H)-dione.
AID1136864Stability of the compound in synthetic growth medium assessed as compound remaining at 37 degC after 16 hrs1979Journal of medicinal chemistry, May, Volume: 22, Issue:5
Synthesis and biological activity of 5-fluoro- and 5-methyl-1,3-oxazine-2,6(3H)-dione.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (11)

TimeframeStudies, This Drug (%)All Drugs %
pre-199010 (90.91)18.7374
1990's1 (9.09)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)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 (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other12 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]