EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C16H12ClFN2O2 |
| Net Charge | 0 |
| Average Mass | 318.735 |
| Monoisotopic Mass | 318.05713 |
| SMILES | CN1C(=O)C(O)N=C(c2ccccc2F)c2cc(Cl)ccc21 |
| InChI | InChI=1S/C16H12ClFN2O2/c1-20-13-7-6-9(17)8-11(13)14(19-15(21)16(20)22)10-4-2-3-5-12(10)18/h2-8,15,21H,1H3 |
| InChIKey | RMFYWNFETXNTIQ-UHFFFAOYSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Phyllostachys violascens (ncbitaxon:1903417) | stem (BTO:0001300) | MetaboLights (MTBLS3970) | Strain: Phyllostachys violascens cv. Viridisulcata |
| 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) |
| Flutemazepam (CHEBI:188885) is a benzodiazepine (CHEBI:22720) |
| IUPAC Name |
|---|
| 7-chloro-5-(2-fluorophenyl)-3-hydroxy-1-methyl-3H-1,4-benzodiazepin-2-one |
| Manual Xrefs | Databases |
|---|---|
| 36859 | ChemSpider |
| Registry Numbers | Sources |
|---|---|
| CAS:52391-89-6 | ChemIDplus |