EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C24H22N2O |
| Net Charge | 0 |
| Average Mass | 354.453 |
| Monoisotopic Mass | 354.17321 |
| SMILES | CCC(=O)N1c2ccccc2N=C(c2ccccc2)CC1c1ccccc1 |
| InChI | InChI=1S/C24H22N2O/c1-2-24(27)26-22-16-10-9-15-20(22)25-21(18-11-5-3-6-12-18)17-23(26)19-13-7-4-8-14-19/h3-16,23H,2,17H2,1H3 |
| InChIKey | QANWFXLRXJOXFE-UHFFFAOYSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Rattus norvegicus (ncbitaxon:10116) | liver (BTO:0000759) | MetaboLights (MTBLS4163) |
| 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) |
| 1-(2,4-diphenyl-2,3-dihydro-1H-1,5-benzodiazepin-1-yl)propan-1-one (CHEBI:190610) is a benzodiazepine (CHEBI:22720) |
| IUPAC Name |
|---|
| 1-(2,4-diphenyl-2,3-dihydro-1,5-benzodiazepin-1-yl)propan-1-one |
| Manual Xrefs | Databases |
|---|---|
| 2010666 | ChemSpider |