Abstract
Investigation of a series 6-[2-(4-aryl-1-piperazinyl)ethyl]-2H-1,4-benzoxazin-3(4H)-ones has led to the discovery of potent 5-HT(1A/1B/1D) receptor antagonists with and without additional SerT affinity. Modulation of the different target activities gave compounds with a range of profiles suitable for further in vivo characterization.
MeSH terms
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Animals
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Antidepressive Agents / chemical synthesis
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Antidepressive Agents / pharmacology
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Benzoxazoles / chemical synthesis*
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Benzoxazoles / pharmacology
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Drug Design
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Humans
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Liver / drug effects
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Liver / metabolism
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Models, Chemical
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Piperazine
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Piperazines / chemical synthesis*
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Piperazines / chemistry
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Piperazines / pharmacology
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Rats
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Selective Serotonin Reuptake Inhibitors / chemical synthesis*
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Selective Serotonin Reuptake Inhibitors / pharmacology*
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Serotonin 5-HT1 Receptor Antagonists
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Serotonin Antagonists / chemical synthesis*
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Serotonin Antagonists / pharmacology*
Substances
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Antidepressive Agents
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Benzoxazoles
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Piperazines
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Serotonin 5-HT1 Receptor Antagonists
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Serotonin Antagonists
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Serotonin Uptake Inhibitors
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Piperazine