EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C16H8ClD5N2O2 |
| Net Charge | 0 |
| Average Mass | 305.776 |
| Monoisotopic Mass | 305.09794 |
| SMILES | [2H]c1c([2H])c([2H])c(C2=NC(O)C(=O)N(C)c3ccc(Cl)cc32)c([2H])c1[2H] |
| InChI | InChI=1S/C16H13ClN2O2/c1-19-13-8-7-11(17)9-12(13)14(18-15(20)16(19)21)10-5-3-2-4-6-10/h2-9,15,20H,1H3/i2D,3D,4D,5D,6D |
| InChIKey | SEQDDYPDSLOBDC-VIQYUKPQSA-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) |
| Temazepam-d5 (CHEBI:228678) is a benzodiazepine (CHEBI:22720) |
| IUPAC Name |
|---|
| 7-chloro-3-hydroxy-1-methyl-5-(2,3,4,5,6-pentadeuteriophenyl)-3H-1,4-benzodiazepin-2-one |
| Manual Xrefs | Databases |
|---|---|
| 27523923 | ChemSpider |