EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C20H19N3O3 |
| Net Charge | 0 |
| Average Mass | 349.390 |
| Monoisotopic Mass | 349.14264 |
| SMILES | O=C1c2cc(O)cc(O)c2N[C@@H](c2cnc3ccccc23)[C@@H]2CCCN12 |
| InChI | InChI=1S/C20H19N3O3/c24-11-8-13-19(17(25)9-11)22-18(16-6-3-7-23(16)20(13)26)14-10-21-15-5-2-1-4-12(14)15/h1-2,4-5,8-10,16,18,21-22,24-25H,3,6-7H2/t16-,18-/m0/s1 |
| InChIKey | IMNRJRPWAJLJKF-WMZOPIPTSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Xenorhabdus eapokensis (ncbitaxon:1873482) | - | PubMed (29596433) |
| 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) |
| Dihydroxy tilivalline (CHEBI:219995) is a benzodiazepine (CHEBI:22720) |
| IUPAC Name |
|---|
| (6S,6aS)-2,4-dihydroxy-6-(1H-indol-3-yl)-5,6,6a,7,8,9-hexahydropyrrolo[2,1-c][1,4]benzodiazepin-11-one |
| Manual Xrefs | Databases |
|---|---|
| 78442858 | ChemSpider |