Abstract
We describe practical and efficient routes for synthesis of 2-aminomethyl-1,2,3,9-tetrahydro-4H-carbazol-4-ones using the Fischer indole synthesis or palladium-catalysed cyclization methodologies, as well as their affinities for D(2), 5-HT(2A) and 5-HT(2C) receptors, and their activity at the 5-HT(2B) receptor. The most active compounds, 4b (QF 2003B) and 4c (QF 2004B), with a pK(i) (5-HT(2A)/D(2)) ratio of 1.28 show a potential antipsychotic profile according to Meltzer's classification.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antipsychotic Agents / chemical synthesis*
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Antipsychotic Agents / metabolism*
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Aorta, Thoracic / drug effects
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Aorta, Thoracic / physiology
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Butyrophenones / chemistry*
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Carbazoles / chemical synthesis
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Carbazoles / chemistry*
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Carbazoles / metabolism
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Carbazoles / pharmacology
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Cattle
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Cell Membrane / metabolism
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Choroid Plexus / metabolism
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Frontal Lobe / metabolism
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Isoxazoles / chemical synthesis
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Isoxazoles / metabolism
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Isoxazoles / pharmacology
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Male
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Piperazines / chemical synthesis
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Piperazines / metabolism
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Piperazines / pharmacology
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Rats
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Rats, Sprague-Dawley
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Receptors, Dopamine D2 / metabolism*
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Receptors, Serotonin / metabolism*
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Serotonin Antagonists / pharmacology
Substances
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Antipsychotic Agents
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Butyrophenones
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Carbazoles
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Isoxazoles
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Piperazines
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QF 2003B
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QF 2004B
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Receptors, Dopamine D2
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Receptors, Serotonin
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Serotonin Antagonists