EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C11H17N3O5 |
| Net Charge | 0 |
| Average Mass | 271.273 |
| Monoisotopic Mass | 271.11682 |
| SMILES | CCCCC1(CCOC(N)=O)C(=O)NC(=O)NC1=O |
| InChI | InChI=1S/C11H17N3O5/c1-2-3-4-11(5-6-19-9(12)17)7(15)13-10(18)14-8(11)16/h2-6H2,1H3,(H2,12,17)(H2,13,14,15,16,18) |
| InChIKey | ZWGPHQZXAPWKOV-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) |
| carbubarb (CHEBI:135116) is a barbiturates (CHEBI:22693) |
| Synonyms | Source |
|---|---|
| carbubarbital | DrugCentral |
| tylemalum | DrugCentral |
| Manual Xrefs | Databases |
|---|---|
| 3702 | DrugCentral |
| Registry Numbers | Sources |
|---|---|
| CAS:960-05-4 | DrugCentral |