Showing Metabocard for 5-hydroxyisourate (BASm0001179)
| Common Name | 5-hydroxyisourate |
|---|---|
| Description | 5-Hydroxyisourate is involved in purine degradation. It is a substrate of the enzyme hydroxyisourate hydrolase which catalyzes the reaction 5-hydroxyisourate + H2O <=> 5-hydroxy-2-oxo-4-ureido-2,5-dihydro-1H-imidazole-5-carboxylate. In most organisms, including some bacteria (such as E. coli), plants, and certain animals, urate is metabolized via a common pathway, producing the stereospecific form S-allantoin as the final product. In the first step of the pathway factor-independent urate hydroxylase catalyzes the conversion of urate to 5-hydroxyisourate. |
| Structure | |
| Molecular Formula | C5H4N4O4 |
| Average Mass | 184.10970 |
| Monoisotopic Mass | 184.02325 |
| IUPAC Name | Not Available |
| Traditional Name | Not Available |
| CAS Registry Number | Not Available |
| SMILES | O=C1N=C2NC(=O)NC2(O)C(=O)N1 |
| InChI Identifier | InChI=1S/C5H4N4O4/c10-2-5(13)1(6-3(11)8-2)7-4(12)9-5/h13H,(H3,6,7,8,9,10,11,12) |
| InChI Key | LTQYPAVLAYVKTK-UHFFFAOYSA-N |
| CHEBI ID | CHEBI:18072 |
| HMDB ID | HMDB30097 |
| MiMeDB ID | MMDBc0031761 |
| State | Expected Solid |
| Water Solubility | Not Available |
| logS | Not Available |
| pKa (Strongest Acidic) | Not Available |
| pKa (Strongest Basic) | Not Available |
| Hydrogen Acceptor Count | Not Available |
| Hydrogen Donor Count | Not Available |
| Rotatable Bond Count | Not Available |
| Physiological Charge | Not Available |
| Formal Charge | Not Available |
| Polarizability | Not Available |