c5URA – 5-Carbouyuracil
| Name | ||
|---|---|---|
| WID | c5URA |
|
| Name | 5-Carbouyuracil |
|
| Traditional name | steviolbioside | |
| IUPAC name | 2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid | |
| Cross references | ChEBI: 17477, PubChem: 8144603, KEGG: C03030 | |
| Classification | ||
| Type | modified_nucleobase |
|
| Structure | ||
| Empirical formula (pH 7.5) | H4C5N2O4 | |
| SMILES (pH 7.5) | N1C=C(C(=O)NC1=O)C(=O)O | |
| Charge (pH 7.5) | -1 | |
| Is hydrophobic | False |
|
| Molecular weight (Da) | 156.10 |
|
| van der Waals volume (pH 7.5; Å3 molecule‑1) |
116.50 | |
| ΔfG'o (pH 7.5, 25C, I = 0; kJ mol‑1) | -428.30 | |
| logP | -1.27 | |
| logD (pH 7.5) | -4.74 | |
| Function | ||
| Reaction participant | DNA radiation (gamma-ray) induced base oxidation (5-formyluracil ==> 5-Carbouyuracil; hydroxyl radical) f5URA[c] + gamma_radiation[e] + hydroxyl_radical[c] ⇒ c5URA[c] + H[c] |
|
| Metadata | ||
| Created | 2012-10-01 15:06:51 | |
| Last updated | 2012-10-01 15:11:56 | |
