Abstract
Syntheses of affinity reagents for opiate receptors based on the fentanyl, endo-ethenotetrahydrooripavine, and etonitazene carbon-nitrogen skeletons are described. The isothiocyanate, bromoacetamido, and methylfumaramido alkylating functions were employed in these compounds, some of which had previously been shown to be mu specific (12, BIT) and delta specific (8, FIT and 19, FAO) in vitro. Antinociceptive activity of the title compounds was determined in the mouse hot-plate test, which revealed that certain compounds in each class showed morphine-like activity. The binding EC50 values against [3H]Dalamid for opiate receptors in NG108-15 (delta receptors) and rat brain membranes (mu + delta receptors) are also reported. With this type of experiment, it was possible to independently measure the apparent affinity of the etonitazene congeners 12-14 for the mu and delta receptors.
MeSH terms
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Animals
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Benzimidazoles / analogs & derivatives
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Benzimidazoles / metabolism
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Benzimidazoles / pharmacology
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Cell Line
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Cell Membrane / metabolism
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Chemical Phenomena
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Chemistry
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Drug Evaluation, Preclinical
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Fentanyl / analogs & derivatives
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Fentanyl / metabolism
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Fentanyl / pharmacology
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Glioma / metabolism
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Hybrid Cells / metabolism
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Indicators and Reagents
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Ligands / metabolism*
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Ligands / pharmacology
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Magnetic Resonance Spectroscopy
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Mass Spectrometry
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Mice
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Narcotic Antagonists / chemical synthesis*
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Neuroblastoma / metabolism
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Rats
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Receptors, Opioid / drug effects
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Receptors, Opioid / metabolism*
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Receptors, Opioid, delta
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Receptors, Opioid, mu
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Structure-Activity Relationship
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Thebaine / analogs & derivatives
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Thebaine / metabolism
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Thebaine / pharmacology
Substances
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Benzimidazoles
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Indicators and Reagents
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Ligands
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Narcotic Antagonists
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Receptors, Opioid
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Receptors, Opioid, delta
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Receptors, Opioid, mu
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Thebaine
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endo-ethenotetrahydrooripavine
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Fentanyl