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Volinanserin
Chemical compound
Chemical compound
| elimination_half-life = 6.6 hours (range 4.5–9.8 hours)
Volinanserin (; developmental code MDL-100,907) is a highly selective 5-HT2A receptor antagonist that is frequently used in scientific research to investigate the function of the 5-HT2A receptor. It was also tested in clinical trials as a potential antipsychotic, antidepressant, and treatment for insomnia but was never marketed. The drug reached phase 3 trials for schizophrenia and insomnia prior to the discontinuation of its development in the late 2000s. It is taken orally.
Pharmacology
Pharmacokinetics
The time to peak levels of volinanserin is 1 to 2.5hours. The elimination half-life of volinanserin is 6.6hours, with a range of 4.5 to 9.8hours. However, cortical serotonin 5-HT2A receptor occupancy with volinanserin measured by positron emission tomography (PET) imaging lasts much longer than its circulating elimination half-life would imply.
Chemistry
Synthesis
The synthesis of volinanserin has been reported. Beginning with protection of ethyl isonipecotate (1) with Boc anhydride gives ethyl N-Boc-4-piperidinecarboxylate (2). Ester-amide interchange with N-methoxymethylamine HCl in the presence of carbonyldiimidazole (CDI) coupling agent gives 1-Boc-4-[methoxy(methyl)carbamoyl]piperidine (3). Weinreb ketone synthesis occurs upon benzoylation with 1,2-dimethoxybenzene (4) to give 1-Boc-4-(2,3-dimethoxybenzoyl)piperidine (5). Acid removal of the urethane protecting group gives (2,3-dimethoxyphenyl)-piperidin-4-ylmethanone (6). The reduction of the ketone with sodium borohydride leads to (2,3-dimethoxyphenyl)-piperidin-4-ylmethanol (7). Resolution of the alcohol gives (8). SN2 alkylation of the secondary nitrogen with 4-fluorophenethyl bromide (9) completes the synthesis of volinanserin (10).
References
References
- (2008). "5-HT(2A) inverse-agonists for the treatment of insomnia". Curr Top Med Chem.
- (May 2009). "Antagonism of serotonergic 5-HT2A/2C receptors: mutual improvement of sleep, cognition and mood?". Eur J Neurosci.
- (June 2022). ""Selective" serotonin 5-HT2A receptor antagonists". Biochem Pharmacol.
- (November 2014). "Positron emission tomography in CNS drug discovery and drug monitoring". J Med Chem.
- (August 1998). "Positron emission tomographic analysis of dose-dependent MDL 100,907 binding to 5-hydroxytryptamine-2A receptors in the human brain". J Clin Psychopharmacol.
- (13 March 2009). "Volinanserin".
- (March 1997). "MDL 100,907: A Selective 5-HT 2A Receptor Antagonist for the Treatment of Schizophrenia". CNS Drug Reviews.
- (November 1992). "5-HT2 receptors exert a state-dependent regulation of dopaminergic function: studies with MDL 100,907 and the amphetamine analogue, 3,4-methylenedioxymethamphetamine". European Journal of Pharmacology.
- (April 2009). "Synthesis and in vitro affinities of various MDL 100907 derivatives as potential 18F-radioligands for 5-HT2A receptor imaging with PET". Bioorganic & Medicinal Chemistry.
- (April 2009). "Blockade of the serotonin 5-HT2A receptor suppresses cue-evoked reinstatement of cocaine-seeking behavior in a rat self-administration model". Behavioral Neuroscience.
- (August 1999). "The role of positron emission tomography in the drug development of M100907, a putative antipsychotic with a novel mechanism of action". Journal of Clinical Pharmacology.
- (July 2013). "Neurobiology of Mental Illness". OUP USA.
- (December 2005). "The selective 5-HT2A receptor antagonist M100907 enhances antidepressant-like behavioral effects of the SSRI fluoxetine". Neuropsychopharmacology.
- (2008). "5-HT(2A) inverse-agonists for the treatment of insomnia". Current Topics in Medicinal Chemistry.
- (September 1997). "Time course of 5-HT2A receptor occupancy in the human brain after a single oral dose of the putative antipsychotic drug MDL 100,907 measured by positron emission tomography". Neuropsychopharmacology.
- (January 2014). "Development of novel chiral capillary electrophoresis methods for the serotonin receptor (5-HT2A) antagonist MDL 100,907 (volinanserin) and for its key intermediate compound". Journal of Pharmaceutical and Biomedical Analysis.
- "(+)-α-(2,3-Dimethoxyphenyl)-1-[2-(4-fluorophenyl)ethyl]-4-piperidinemethanol".
- (1999). "An efficient synthesis of the precursors of [11C]MDL 100907 labeled in two specific positions". Journal of Labelled Compounds and Radiopharmaceuticals.
- "Pharmaceutical composition containing a 5HT2c antagonist and a D2 antagonist".
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