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CHEBI:7735 - olanzapine
| Formula | C17H20N4S |
| Net Charge | 0 |
| Average Mass | 312.442 |
| Monoisotopic Mass | 312.14087 |
| SMILES | Cc1cc2c(s1)Nc1ccccc1N=C2N1CCN(C)CC1 |
| InChI | InChI=1S/C17H20N4S/c1-12-11-13-16(21-9-7-20(2)8-10-21)18-14-5-3-4-6-15(14)19-17(13)22-12/h3-6,11,19H,7-10H2,1-2H3 |
| InChIKey | KVWDHTXUZHCGIO-UHFFFAOYSA-N |
| Wikipedia |
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| Roles Classification |
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| Chemical Role: | Bronsted base A molecular entity capable of accepting a hydron from a donor (Brønsted acid). |
| Biological Roles: | histamine antagonist Histamine antagonists are the drugs that bind to but do not activate histamine receptors, thereby blocking the actions of histamine or histamine agonists. anti-obesity agent Any substance which is used to reduce or control weight. serotonin uptake inhibitor A compound that specifically inhibits the reuptake of serotonin in the brain. This increases the serotonin concentration in the synaptic cleft which then activates serotonin receptors to a greater extent. serotonergic antagonist Drugs that bind to but do not activate serotonin receptors, thereby blocking the actions of serotonin or serotonergic agonists. muscarinic antagonist A drug that binds to but does not activate muscarinic cholinergic receptors, thereby blocking the actions of endogenous acetylcholine or exogenous agonists. dopaminergic antagonist A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists. 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: | antiemetic A drug used to prevent nausea or vomiting. An antiemetic may act by a wide range of mechanisms: it might affect the medullary control centres (the vomiting centre and the chemoreceptive trigger zone) or affect the peripheral receptors. antineoplastic agent A substance that inhibits or prevents the proliferation of neoplasms. antidepressant Antidepressants are mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions. histamine antagonist Histamine antagonists are the drugs that bind to but do not activate histamine receptors, thereby blocking the actions of histamine or histamine agonists. serotonin uptake inhibitor A compound that specifically inhibits the reuptake of serotonin in the brain. This increases the serotonin concentration in the synaptic cleft which then activates serotonin receptors to a greater extent. second generation antipsychotic Antipsychotic drugs which can have different modes of action but which tend to be less likely than first generation antipsychotics to cause extrapyramidal motor control disabilities such as body rigidity or Parkinson's disease-type movements. appetite enhancer A drug which increases appetite. serotonergic antagonist Drugs that bind to but do not activate serotonin receptors, thereby blocking the actions of serotonin or serotonergic agonists. muscarinic antagonist A drug that binds to but does not activate muscarinic cholinergic receptors, thereby blocking the actions of endogenous acetylcholine or exogenous agonists. 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. dopaminergic antagonist A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists. 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) |
| olanzapine (CHEBI:7735) has role anti-obesity agent (CHEBI:74518) |
| olanzapine (CHEBI:7735) has role antidepressant (CHEBI:35469) |
| olanzapine (CHEBI:7735) has role antiemetic (CHEBI:50919) |
| olanzapine (CHEBI:7735) has role antineoplastic agent (CHEBI:35610) |
| olanzapine (CHEBI:7735) has role anxiolytic drug (CHEBI:35474) |
| olanzapine (CHEBI:7735) has role appetite enhancer (CHEBI:50779) |
| olanzapine (CHEBI:7735) has role dopaminergic antagonist (CHEBI:48561) |
| olanzapine (CHEBI:7735) has role histamine antagonist (CHEBI:37956) |
| olanzapine (CHEBI:7735) has role muscarinic antagonist (CHEBI:48876) |
| olanzapine (CHEBI:7735) has role second generation antipsychotic (CHEBI:65191) |
| olanzapine (CHEBI:7735) has role serotonergic antagonist (CHEBI:48279) |
| olanzapine (CHEBI:7735) has role serotonin uptake inhibitor (CHEBI:50949) |
| olanzapine (CHEBI:7735) is a N-arylpiperazine (CHEBI:46848) |
| olanzapine (CHEBI:7735) is a N-methylpiperazine (CHEBI:46920) |
| olanzapine (CHEBI:7735) is a benzodiazepine (CHEBI:22720) |
| IUPAC Name |
|---|
| 2-methyl-4-(4-methylpiperazin-1-yl)-10H-thieno[2,3-b][1,5]benzodiazepine |
| INNs | Source |
|---|---|
| olanzapina | ChEBI |
| olanzapine | ChEBI |
| olanzapinum | ChEBI |
| Synonyms | Source |
|---|---|
| LY170053 | ChEMBL |
| Olansek | ChEMBL |
| Olanzapine | KEGG COMPOUND |
| Olanzapine apotex | ChEMBL |
| Olanzapine cipla | ChEMBL |
| Olanzapine glenmark | ChEMBL |
| Brand Names | Source |
|---|---|
| Arkolamyl | ChEMBL |
| Olanzapine cipla (previously olanzapine neopharma) | ChEMBL |
| Olanzapine component of lybalvi | ChEMBL |
| Olanzapine component of symbyax | ChEMBL |
| Olanzapine glenmark europe | ChEMBL |
| Zalasta | ChEMBL |
| Registry Numbers | Sources |
|---|---|
| Reaxys:7655141 | Reaxys |
| CAS:132539-06-1 | ChemIDplus |
| Citations |
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