EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C16H7D7FN3O |
| Net Charge | 0 |
| Average Mass | 290.349 |
| Monoisotopic Mass | 290.15603 |
| SMILES | [2H]c1c([2H])c([2H])c(C2=NCC(=O)N(C([2H])([2H])[2H])c3ccc(N)cc32)c(F)c1[2H] |
| InChI | InChI=1S/C16H14FN3O/c1-20-14-7-6-10(18)8-12(14)16(19-9-15(20)21)11-4-2-3-5-13(11)17/h2-8H,9,18H2,1H3/i1D3,2D,3D,4D,5D |
| InChIKey | LTCDLGUFORGHGY-AAYPNNLASA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Homo sapiens (ncbitaxon:9606) | urine (BTO:0001419) | MetaboLights (MTBLS8662) |
| 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-Aminoflunitrazepam-d7 (CHEBI:228431) is a benzodiazepine (CHEBI:22720) |
| IUPAC Name |
|---|
| 7-amino-5-(2,3,4,5-tetradeuterio-6-luorophenyl)-1-(trideuteriomethyl)-3H-1,4-benzodiazepin-2-one |
| Manual Xrefs | Databases |
|---|---|
| 32675190 | ChemSpider |