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CHEBI:5121 - flupenthixol
| Formula | C23H27F3N2OS |
| Net Charge | 0 |
| Average Mass | 436.543 |
| Monoisotopic Mass | 436.17962 |
| SMILES | [H]C(CCN1CCN(CCO)CC1)=C1c2ccccc2SC2C=CC(C(F)(F)F)=CC12 |
| InChI | InChI=1S/C23H27F3N2OS/c24-23(25,26)17-7-8-22-20(16-17)18(19-4-1-2-6-21(19)30-22)5-3-9-27-10-12-28(13-11-27)14-15-29/h1-2,4-8,16,20,22,29H,3,9-15H2 |
| InChIKey | DTTVNHWDONBIKE-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: | dopaminergic antagonist A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists. alpha-adrenergic antagonist An agent that binds to but does not activate α-adrenergic receptors thereby blocking the actions of endogenous or exogenous α-adrenergic agonists. α-Adrenergic antagonists are used in the treatment of hypertension, vasospasm, peripheral vascular disease, shock, and pheochromocytoma. EC 3.4.21.26 (prolyl oligopeptidase) inhibitor Any EC 3.4.21.* (serine endopeptidase) inhibitor that interferes with the action of prolyl oligopeptidase (EC 3.4.21.26). |
| Applications: | dopaminergic antagonist A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists. alpha-adrenergic antagonist An agent that binds to but does not activate α-adrenergic receptors thereby blocking the actions of endogenous or exogenous α-adrenergic agonists. α-Adrenergic antagonists are used in the treatment of hypertension, vasospasm, peripheral vascular disease, shock, and pheochromocytoma. first generation antipsychotic Antipsychotic drugs which can have different modes of action but which tend to be more likely than second generation antipsychotics to cause extrapyramidal motor control disabilities such as body rigidity or Parkinson's disease-type movements; such body movements can become permanent even after treatment has ceased. 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. antidepressant Antidepressants are mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions. |
| ChEBI Ontology |
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| Outgoing Relation(s) |
| flupenthixol (CHEBI:5121) has role antidepressant (CHEBI:35469) |
| flupenthixol (CHEBI:5121) has role anxiolytic drug (CHEBI:35474) |
| flupenthixol (CHEBI:5121) has role dopaminergic antagonist (CHEBI:48561) |
| flupenthixol (CHEBI:5121) has role EC 3.4.21.26 (prolyl oligopeptidase) inhibitor (CHEBI:76779) |
| flupenthixol (CHEBI:5121) has role first generation antipsychotic (CHEBI:65190) |
| flupenthixol (CHEBI:5121) has role α-adrenergic antagonist (CHEBI:37890) |
| flupenthixol (CHEBI:5121) is a N-alkylpiperazine (CHEBI:46845) |
| flupenthixol (CHEBI:5121) is a fluorine molecular entity (CHEBI:24062) |
| flupenthixol (CHEBI:5121) is a primary alcohol (CHEBI:15734) |
| flupenthixol (CHEBI:5121) is a thioxanthenes (CHEBI:50930) |
| Incoming Relation(s) |
| cis-flupenthixol (CHEBI:10454) is a flupenthixol (CHEBI:5121) |
| IUPAC Name |
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| 2-(4-{3-[2-(trifluoromethyl)-4a,9a-dihydro-9H-thioxanthen-9-ylidene]propyl}piperazin-1-yl)ethanol |
| INNs | Source |
|---|---|
| flupentixol | ChemIDplus |
| flupentixol | WHO MedNet |
| Synonyms | Source |
|---|---|
| flupentixolum | WHO MedNet |
| 2-Trifluoromethyl-9-(3-(4-(2-hydroxyethyl)piperazin-1-yl)propylidene)thioxanthene | ChemIDplus |
| 2-Trifluoromethyl-9-(3-(4-(beta-hydroxyethyl)-1-piperazinyl)propylidene)thioxanthene | ChemIDplus |
| 4-(3-(2-(Trifluoromethyl)-9H-thioxanthen-9-ylidene)propyl)-1-piperazineethanol | ChemIDplus |
| 4-(3-(2-(Trifluoromethyl)thioxanthen-9-ylidene)propyl)-1-piperazineethanol | ChemIDplus |
| Citations |
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