Short description: Chemical compound
Moperone |
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| Trade names | Luvatren (discontinued) |
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| Identifiers |
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IUPAC name
1-(4-fluorophenyl)-4-[4-hydroxy-4-(4-methylphenyl)piperidin-1-yl]butan-1-one
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| Chemical and physical data |
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| Formula | C22H26FNO2 |
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| Molar mass | 355.453 g·mol−1 |
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| 3D model (JSmol) | |
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SMILES
CC1=CC=C(C=C1)C1(O)CCN(CCCC(=O)C2=CC=C(F)C=C2)CC1
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InChI
InChI=1S/C22H26FNO2/c1-17-4-8-19(9-5-17)22(26)12-15-24(16-13-22)14-2-3-21(25)18-6-10-20(23)11-7-18/h4-11,26H,2-3,12-16H2,1H3 Key:AGAHNABIDCTLHW-UHFFFAOYSA-N
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Moperone (Luvatren, since discontinued) is a typical antipsychotic of the butyrophenone class[1] which is marketed in Japan for the treatment of schizophrenia. It is an antagonist for the D2 (Ki 0.7–1.9 nM), D3 (Ki 0.1–1 nM), and 5-HT2A (Ki 52 nM) receptors. It also has a high binding affinity for the sigma receptors.[2][3]
References
- ↑ Gross, H; Kaltenbäck, E (1969). "The clinical position of moperone among the butyrophenones". Nordisk Psykiatrisk Tidsskrift. Nordic Journal of Psychiatry 23 (1): 4–9. doi:10.3109/08039486909132154. PMID 5354545.
- ↑ "Moperone" (in en). Encyclopedia of Psychopharmacology. Berlin, Heidelberg: Springer. 2010. pp. 798. doi:10.1007/978-3-540-68706-1_1838. ISBN 978-3-540-68706-1. https://doi.org/10.1007/978-3-540-68706-1_1838. Retrieved 21 March 2022.
- ↑ "PDSP Ki Database". Psychoactive Drug Screening Program (PDSP). University of North Carolina at Chapel Hill and the United States National Institute of Mental Health. https://pdsp.unc.edu/databases/pdsp.php?receptorDD=&receptor=&speciesDD=&species=&sourcesDD=&source=&hotLigandDD=&hotLigand=&testLigandDD=&testFreeRadio=testFreeRadio&testLigand=moperone&referenceDD=&reference=&KiGreater=&KiLess=&kiAllRadio=all&doQuery=Submit+Query.
Antipsychotics (N05A) |
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| Typical |
- Butyrophenones: Benperidol
- Bromperidol
- Droperidol
- Haloperidol#
- Moperone
- Pipamperone
- Spiperone
- Timiperone
- Trifluperidol
- Diphenylbutylpiperidines: Fluspirilene
- Penfluridol
- Pimozide
- Phenothiazines: Acetophenazine
- Butaperazine
- Carphenazine (carfenazine)‡
- Chlorpromazine
- Cyamemazine
- Dixyrazine
- Fluphenazine
- Levomepromazine (methotrimeprazine)
- Mesoridazine
- Perazine
- Periciazine
- Perphenazine
- Piperacetazine
- Pipotiazine
- Prochlorperazine
- Promazine
- Sulforidazine
- Thiopropazate
- Thioproperazine
- Thioridazine
- Trifluoperazine
- Triflupromazine
- Thioxanthenes: Chlorprothixene
- Clopenthixol
- Flupentixol
- Tiotixene (thiothixene)
- Zuclopenthixol
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| Disputed |
- Benzamides: Amisulpride
- Levosulpiride
- Nemonapride
- Remoxipride‡
- Sulpiride
- Sultopride
- Tiapride
- Veralipride‡
- Butyrophenones: Melperone
- Tricyclics: Carpipramine
- Clocapramine
- Clorotepine
- Clotiapine
- Loxapine
- Mosapramine
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| Atypical |
- Benzisoxazole/benzisothiazoles: Iloperidone
- Lurasidone
- Paliperidone
- Paliperidone palmitate
- Perospirone
- Risperidone#
- Ziprasidone
- Butyrophenones: Lumateperone†
- Phenylpiperazines/quinolinones: Aripiprazole
- Aripiprazole lauroxil
- Brilaroxazine†
- Brexpiprazole
- Cariprazine
- Tricyclics: Asenapine
- Clozapine#
- Olanzapine
- Quetiapine
- Zotepine
- Others: Blonanserin
- Pimavanserin
- Sertindole
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| Others |
- Azacyclonol
- Cannabidiol
- Oxypertine
- Reserpine
- Tetrabenazine
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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 | Original source: https://en.wikipedia.org/wiki/Moperone. Read more |