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CHEBI:111762 - nordazepam
| Formula | C15H11ClN2O |
| Net Charge | 0 |
| Average Mass | 270.719 |
| Monoisotopic Mass | 270.05599 |
| SMILES | O=C1CN=C(c2ccccc2)c2cc(Cl)ccc2N1 |
| InChI | InChI=1S/C15H11ClN2O/c16-11-6-7-13-12(8-11)15(17-9-14(19)18-13)10-4-2-1-3-5-10/h1-8H,9H2,(H,18,19) |
| InChIKey | AKPLHCDWDRPJGD-UHFFFAOYSA-N |
| Wikipedia |
|---|
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Homo sapiens (ncbitaxon:9606) | - | DOI (10.1038/nbt.2488) |
| Roles Classification |
|---|
| Biological Roles: | 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. human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). 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. |
| Applications: | sedative A central nervous system depressant used to induce drowsiness or sleep or to reduce psychological excitement or anxiety. anxiolytic drug Anxiolytic drugs are agents that alleviate anxiety, tension, and anxiety disorders, promote sedation, and have a calming effect without affecting clarity of consciousness or neurologic conditions. anticonvulsant A drug used to prevent seizures or reduce their severity. 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. 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) |
| nordazepam (CHEBI:111762) has role anticonvulsant (CHEBI:35623) |
| nordazepam (CHEBI:111762) has role anxiolytic drug (CHEBI:35474) |
| nordazepam (CHEBI:111762) has role GABA modulator (CHEBI:50268) |
| nordazepam (CHEBI:111762) has role human metabolite (CHEBI:77746) |
| nordazepam (CHEBI:111762) has role sedative (CHEBI:35717) |
| nordazepam (CHEBI:111762) is a 1,4-benzodiazepinone (CHEBI:35500) |
| nordazepam (CHEBI:111762) is a organochlorine compound (CHEBI:36683) |
| IUPAC Name |
|---|
| 7-chloro-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one |
| INNs | Source |
|---|---|
| nordazepam | ChemIDplus |
| nordazepamum | ChemIDplus |
| Synonyms | Source |
|---|---|
| 1-Demethyldiazepam | ChemIDplus |
| 7-Chloro-1,3-dihydro-5-phenyl-(2H)-1,4-benzodiazepin-2-one | KEGG COMPOUND |
| 7-Chloro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one | ChemIDplus |
| 7-Chloro-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one | NIST Chemistry WebBook |
| Chlordesmethyldiazepam | ChemIDplus |
| Chlordesmethyldiazepam | NIST Chemistry WebBook |
| Citations |
|---|