5-Formyluracil
 | |
| Names | |
|---|---|
| IUPAC name
2,4-Dioxo-1,2,3,4-tetrahydro-5-pyrimidinecarbaldehyde | |
| Identifiers | |
| 1195-08-0 | |
| 3D model (Jmol) | Interactive image |
| ChemSpider | 269368 |
| ECHA InfoCard | 100.153.693 |
| |
| |
| Properties | |
| C5H4N2O3 | |
| Molar mass | 140.10 g·mol−1 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
5-Formyluracil is produced from the oxidation of the methyl group of thymine. It is mutagenic.[1]
References
- ↑ "5-Formyluracil and its nucleoside derivatives confer toxicity and mutagenicity to mammalian cells by interfering with normal RNA and DNA metabolism. - PubMed - NCBI". Ncbi.nlm.nih.gov. Retrieved August 5, 2015.
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