EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C5H6N2O3 |
| Net Charge | 0 |
| Average Mass | 142.114 |
| Monoisotopic Mass | 142.03784 |
| SMILES | O=c1ncc(CO)c(=O)n1 |
| InChI | InChI=1S/C5H6N2O3/c8-2-3-1-6-5(10)7-4(3)9/h1,8H,2H2,(H2,6,7,9,10) |
| InChIKey | JDBGXEHEIRGOBU-UHFFFAOYSA-N |
| Roles Classification |
|---|
| Biological Role: | human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| 5-hydroxymethyluracil (CHEBI:16964) has functional parent uracil (CHEBI:17568) |
| 5-hydroxymethyluracil (CHEBI:16964) has role human metabolite (CHEBI:77746) |
| 5-hydroxymethyluracil (CHEBI:16964) is a primary alcohol (CHEBI:15734) |
| 5-hydroxymethyluracil (CHEBI:16964) is a pyrimidone (CHEBI:38337) |
| Incoming Relation(s) |
| (β-D-glucopyranosyloxymethyl)deoxyuridine (CHEBI:111513) has functional parent 5-hydroxymethyluracil (CHEBI:16964) |
| (β-D-glucopyranosyloxymethyl)deoxyuridine 5'-monophosphate (CHEBI:111511) has functional parent 5-hydroxymethyluracil (CHEBI:16964) |
| 5-formyluracil (CHEBI:80961) has functional parent 5-hydroxymethyluracil (CHEBI:16964) |
| 5-hydroxymethyl-2'-deoxyuridine (CHEBI:61288) has functional parent 5-hydroxymethyluracil (CHEBI:16964) |
| IUPAC Name |
|---|
| 5-(hydroxymethyl)pyrimidine-2,4(1H,3H)-dione |
| Synonyms | Source |
|---|---|
| 5-(hydroxymethyl)-2,4(1H,3H)-pyrimidinedione | ChemIDplus |
| 5-Hydroxymethyluracil | KEGG COMPOUND |
| 5-HYDROXYMETHYL URACIL | PDBeChem |
| 5-(hydroxymethyl)uracil | ChemIDplus |
| UniProt Name | Source |
|---|---|
| 5-hydroxymethyluracil | UniProt |
| Manual Xrefs | Databases |
|---|---|
| C03088 | KEGG COMPOUND |
| CPD-254 | MetaCyc |
| HMDB0000469 | HMDB |
| HMU | PDBeChem |
| Registry Numbers | Sources |
|---|---|
| Reaxys:125482 | Reaxys |
| CAS:4433-40-3 | ChemIDplus |
| CAS:4433-40-3 | KEGG COMPOUND |
| Citations |
|---|