EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C18H21N3O4 |
| Net Charge | 0 |
| Average Mass | 343.383 |
| Monoisotopic Mass | 343.15321 |
| SMILES | COc1cccc2c1N[C@H](O)[C@@H]1CC(/C=C/C(=O)N(C)C)=CN1C2=O |
| InChI | InChI=1S/C18H21N3O4/c1-20(2)15(22)8-7-11-9-13-17(23)19-16-12(18(24)21(13)10-11)5-4-6-14(16)25-3/h4-8,10,13,17,19,23H,9H2,1-3H3/b8-7+/t13-,17+/m0/s1 |
| InChIKey | OQMYRVPMCIOFHL-UDBCLFQLSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Streptomyces (ncbitaxon:1883) | - | PubMed (3192492) |
| 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) |
| Porothramycin A (CHEBI:204009) is a benzodiazepine (CHEBI:22720) |
| IUPAC Name |
|---|
| (E)-3-[(6R,6aS)-6-hydroxy-4-methoxy-11-oxo-5,6,6a,7-tetrahydropyrrolo[2,1-c][1,4]benzodiazepin-8-yl]-N,N-dimethylprop-2-enamide |
| Manual Xrefs | Databases |
|---|---|
| 28287841 | ChemSpider |