EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C18H16N2O4 |
| Net Charge | 0 |
| Average Mass | 324.336 |
| Monoisotopic Mass | 324.11101 |
| SMILES | COc1ccc2c(c1)C(=O)N(C)[C@]1(O[C@H]1c1ccccc1)C(=O)N2 |
| InChI | InChI=1S/C18H16N2O4/c1-20-16(21)13-10-12(23-2)8-9-14(13)19-17(22)18(20)15(24-18)11-6-4-3-5-7-11/h3-10,15H,1-2H3,(H,19,22)/t15-,18+/m0/s1 |
| InChIKey | YIOVFAKRHWSIKG-MAUKXSAKSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Aspergillus (ncbitaxon:5052) | - | PubMed (28074949) |
| 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) |
| 7-methoxycyclopenin (CHEBI:207088) is a benzodiazepine (CHEBI:22720) |
| IUPAC Name |
|---|
| (3R,3'S)-7-methoxy-4-methyl-3'-phenylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione |
| Manual Xrefs | Databases |
|---|---|
| 60958445 | ChemSpider |