![]() | |
Names | |
---|---|
IUPAC name
5-Hydroxy-2,4-imidazolidinedione
| |
Other names
Glyoxalurea; Allanturic acid
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C3H4N2O3 | |
Molar mass | 116.076 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
5-Hydroxyhydantoin is an oxidation product of 2′-deoxycytidine. If not repaired, it may be processed by DNA polymerases that induce mutagenic processes. [1]
![]() | |
Names | |
---|---|
IUPAC name
5-Hydroxy-2,4-imidazolidinedione
| |
Other names
Glyoxalurea; Allanturic acid
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C3H4N2O3 | |
Molar mass | 116.076 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
5-Hydroxyhydantoin is an oxidation product of 2′-deoxycytidine. If not repaired, it may be processed by DNA polymerases that induce mutagenic processes. [1]