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CHEBI:134923 - talbutal
| Formula | C11H16N2O3 |
| Net Charge | 0 |
| Average Mass | 224.260 |
| Monoisotopic Mass | 224.11609 |
| SMILES | C=CCC1(C(C)CC)C(=O)NC(=O)NC1=O |
| InChI | InChI=1S/C11H16N2O3/c1-4-6-11(7(3)5-2)8(14)12-10(16)13-9(11)15/h4,7H,1,5-6H2,2-3H3,(H2,12,13,14,15,16) |
| InChIKey | BJVVMKUXKQHWJK-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) |
| talbutal (CHEBI:134923) is a barbiturates (CHEBI:22693) |
| Synonyms | Source |
|---|---|
| 5-Allyl-5-(1-methylpropyl) barbituric acid | DrugCentral |
| 5-Allyl-5-sec-butylbarbituric acid | DrugCentral |
| lotusate | DrugCentral |
| profundol | DrugCentral |
| Manual Xrefs | Databases |
|---|---|
| 2556 | DrugCentral |
| Registry Numbers | Sources |
|---|---|
| CAS:115-44-6 | DrugCentral |