EMBL-EBI | Chemical Biology | ChEBI
Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search
| Formula | C20H26N4O3 |
| Net Charge | 0 |
| Average Mass | 370.453 |
| Monoisotopic Mass | 370.20049 |
| SMILES | C=CCN1C(=O)NC(=O)C(=C(CC)Nc2ccc(N(CC)CC)cc2)C1=O |
| InChI | InChI=1S/C20H26N4O3/c1-5-13-24-19(26)17(18(25)22-20(24)27)16(6-2)21-14-9-11-15(12-10-14)23(7-3)8-4/h5,9-12,21H,1,6-8,13H2,2-4H3,(H,22,25,27) |
| InChIKey | GJGHQVXAHIPWOE-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) |
| 5-[1-[4-(diethylamino)anilino]propylidene]-1-prop-2-enyl-1,3-diazinane-2,4,6-trione (CHEBI:108197) is a barbiturates (CHEBI:22693) |
| Manual Xrefs | Databases |
|---|---|
| LSM-19574 | LINCS |