EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C12H12N2O4 |
| Net Charge | 0 |
| Average Mass | 248.238 |
| Monoisotopic Mass | 248.07971 |
| SMILES | CCC1(c2ccc(O)cc2)C(=O)NC(=O)NC1=O |
| InChI | InChI=1S/C12H12N2O4/c1-2-12(7-3-5-8(15)6-4-7)9(16)13-11(18)14-10(12)17/h3-6,15H,2H2,1H3,(H2,13,14,16,17,18) |
| InChIKey | IEPXMKJNWPXDBP-UHFFFAOYSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Homo sapiens (ncbitaxon:9606) | pancreas (BTO:0000988) | MetaboLights (MTBLS1925) | Strain: PANC-1 cell [BCGO:0000122] |
| 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) |
| 4-Hydroxyphenobarbital (CHEBI:180569) is a barbiturates (CHEBI:22693) |
| IUPAC Name |
|---|
| 5-ethyl-5-(4-hydroxyphenyl)-1,3-diazinane-2,4,6-trione |
| Manual Xrefs | Databases |
|---|---|
| 9402 | ChemSpider |
| HMDB0060537 | HMDB |
| Registry Numbers | Sources |
|---|---|
| CAS:379-34-0 | ChemIDplus |