| Systematic (IUPAC) name | |
|---|---|
| 3-[4-(4-phenyl-3,6-dihydro-2H-pyridin-1-yl)butyl]-1H-indol-5-ol | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| CAS number | 112192-04-8 |
| ATC code | None |
| PubChem | CID 219050 |
| IUPHAR ligand | 52 |
| ChemSpider | 189880 |
| UNII | 43227SMS0O |
| Chemical data | |
| Formula | C23H26N2O |
| Mol. mass | 346.47 g/mol |
| SMILES | eMolecules & PubChem |
Roxindole (EMD-49,980) is a dopaminergic and serotonergic drug which was originally developed for the treatment of schizophrenia.[1][2][3] In clinical trials its antipsychotic efficacy was only modest but it was unexpectedly found to produce potent and rapid antidepressant and anxiolytic effects.[2][3] As a result, roxindole was further researched for the treatment of depression instead.[1][4][4] It has also been investigated as a therapy for Parkinson's disease and prolactinoma.[5][6]
Roxindole acts as an agonist at the following receptors:[7][8]
At D2 and possibly D3 receptors roxindole is a partial agonist with preferential actions at autoreceptors and has been touted as a 'selective' autoreceptor agonist, hence the justification of its application as an antipsychotic.[9][10] It is also a serotonin reuptake inhibitor (IC50 = 1.4 nM) and has been reported to act as a 5-HT2A receptor antagonist as well.[8][9][10][11]
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