EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C4H4N2O4 |
| Net Charge | 0 |
| Average Mass | 144.086 |
| Monoisotopic Mass | 144.01711 |
| SMILES | O=C1NC(=O)C(O)C(=O)N1 |
| InChI | InChI=1S/C4H4N2O4/c7-1-2(8)5-4(10)6-3(1)9/h1,7H,(H2,5,6,8,9,10) |
| InChIKey | BVEWMNTVZPFPQI-UHFFFAOYSA-N |
| Roles Classification |
|---|
| Biological Role: | GABA modulator A substance that does not act as agonist or antagonist but does affect the gamma-aminobutyric acid receptor-ionophore complex. GABA-A receptors appear to have at least three allosteric sites at which modulators act: a site at which benzodiazepines act by increasing the opening frequency of gamma-aminobutyric acid-activated chloride channels; a site at which barbiturates act to prolong the duration of channel opening; and a site at which some steroids may act. |
| Application: | GABA modulator A substance that does not act as agonist or antagonist but does affect the gamma-aminobutyric acid receptor-ionophore complex. GABA-A receptors appear to have at least three allosteric sites at which modulators act: a site at which benzodiazepines act by increasing the opening frequency of gamma-aminobutyric acid-activated chloride channels; a site at which barbiturates act to prolong the duration of channel opening; and a site at which some steroids may act. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| dialuric acid (CHEBI:76452) has functional parent barbituric acid (CHEBI:16294) |
| dialuric acid (CHEBI:76452) is a barbiturates (CHEBI:22693) |
| dialuric acid (CHEBI:76452) is conjugate acid of dialurate (CHEBI:140629) |
| Incoming Relation(s) |
| dialurate (CHEBI:140629) is conjugate base of dialuric acid (CHEBI:76452) |
| IUPAC Name |
|---|
| 5-hydroxypyrimidine-2,4,6(1H,3H,5H)-trione |
| Synonyms | Source |
|---|---|
| 5-hydroxybarbituric acid | ChemIDplus |
| 2,4,5,6-pyrimidinetetrol | ChemIDplus |
| 5-alloxanol | ChEBI |
| Citations |
|---|