5-Hydroxyhydantoin
Names | |
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IUPAC name
5-Hydroxy-2,4-imidazolidinedione | |
Other names
Glyoxalurea; Allanturic acid | |
Identifiers | |
29410-13-7 | |
Jmol interactive 3D | Image |
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Properties | |
C3H4N2O3 | |
Molar mass | 116.08 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-Hydroxyhydantoin is an oxidation product of 2′-deoxycytidine. If not repaired, it may be processed by DNA polymerases that induce mutagenic processes.[1]
References
- ↑ "Excision of the oxidatively formed 5-hydroxyhydantoin and 5-hydroxy-5-methylhydantoin pyrimidine lesions by Escherichia coli and Saccharomyces cerevisiae DNA N-glycosylases". Sciencedirect.com. Retrieved August 5, 2015.
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