Weight | 420.488 g/mol |
---|---|
Formula | C24H25FN4O2 |
Hydrogen Acceptors | 6 |
Hydrogen Donors | 0 |
Aromatic Rings | 4 |
Rotatable Bonds | 4 |
Ocaperidone (129029-23-8)
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- In vitro and in vivo receptor binding and effects on monoamine turnover in rat brain regions of the novel antipsychotics risperidone and ocaperidone. (Molecular Pharmacology, 1992)
- Behavioral disinhibition and depression in amphetaminized rats: a comparison of risperidone, ocaperidone and haloperidol. (Journal of Pharmacology and Experimental Therapeutics, 1992)
- Pharmacological profile of the new potent neuroleptic ocaperidone (R 79,598). (Journal of Pharmacology and Experimental Therapeutics, 1992)
- Antipsychotic profile and side-effect liability of haloperidol, risperidone, and ocaperidone as predicted from their differential interaction with amphetamine in rats (Drug Development Research, 1992)
- Structure of the antipsychotic drug 3-{2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl}-2,9-dimethyl-4H-pyrido[1,2-a]pyrimidin-4-one (ocaperidone) (Acta Crystallographica Section C-crystal Structure Communications, 1992)
- Ocaperidone-containing composition (2006)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC=CN2C1=NC(=C(C2=O)CCN3CCC(CC3)C4=NOC5=C4C=CC(=C5)F)C
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InChIKeyZZQNEJILGNNOEP-UHFFFAOYSA-N
- Pubchem - Ocaperidone
- Wikipedia - ocaperidone
Ocaperidone (also R 79598) is a benzisoxazole antipsychotic. It was initially developed by Janssen, later licensed to French laboratory Neuro3D and then acquired in 2007 by German company Evotec. Its testing was abandoned after phase II trials, as of 22 February 2010.
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