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CHEBI:135199 - propallylonal
| Formula | C10H13BrN2O3 |
| Net Charge | 0 |
| Average Mass | 289.129 |
| Monoisotopic Mass | 288.01095 |
| SMILES | C=C(Br)CC1(C(C)C)C(=O)NC(=O)NC1=O |
| InChI | InChI=1S/C10H13BrN2O3/c1-5(2)10(4-6(3)11)7(14)12-9(16)13-8(10)15/h5H,3-4H2,1-2H3,(H2,12,13,14,15,16) |
| InChIKey | KTGWBBOJAGDSHN-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) |
| propallylonal (CHEBI:135199) is a barbiturates (CHEBI:22693) |
| Synonyms | Source |
|---|---|
| bromoaprobarbital | DrugCentral |
| ibomal | DrugCentral |
| propaldon | DrugCentral |
| Manual Xrefs | Databases |
|---|---|
| 3492 | DrugCentral |
| Registry Numbers | Sources |
|---|---|
| CAS:545-93-7 | DrugCentral |