Dihydrouracil
Names | |
---|---|
Preferred IUPAC name 1,3-Diazinane-2,4-dione | |
Other names Dihydropyrimidine-2,4(1H,3H)-dione | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChemSpider |
|
ECHA InfoCard | 100.007.257 |
MeSH | Dihydrouracil |
PubChem CID |
|
UNII |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | C4H6N2O2 |
Molar mass | 114.10264 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references |
Chemical compound
Dihydrouracil is an intermediate in the catabolism of uracil.[1] It is the base present in the nucleoside dihydrouridine.
See also
- Dihydrouracil dehydrogenase (NAD+)
- Dihydrouracil oxidase
- Dihydropyrimidinase
References
- ^ Nakamura, A; Kikuchi, K; Ohishi, T; Masuike, T (March 2004). "[Assay method for uracil, dihydrouracil, 5-fluorouracil and 5-fluoro-5, 6-dihydrouracil by high-performance liquid chromatography]". Gan to Kagaku Ryoho. Cancer & Chemotherapy. 31 (3): 381–6. PMID 15045945.
- v
- t
- e
Nucleotide metabolic intermediates
metabolism
anabolism |
| ||||||
---|---|---|---|---|---|---|---|
catabolism |
metabolism
anabolism | |||||
---|---|---|---|---|---|
catabolism |
|
This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
- v
- t
- e