Abstract
A novel 6,14-epoxymorphinan benzamide derivative (NS22) that was previously reported showed opioid κ receptor agonistic activity and analgesic activity. The unsatisfactory κ selectivity of NS22 led us to synthesize its derivatives to improve the opioid κ receptor selectivity and the agonist activity. In the course of SAR of the various derivatives, 17-benzyl-6,14-epoxymorphinan derivatives (KNT-33, 53, 55, 80, 90, 133) were found to show high selectivities and affinities for the opioid κ receptor. In addition, KNT-33, 53, 55 showed dose-dependent analgesic effects in acetic acid writhing tests. Therefore, 17-benzyl substituents may play an important role for developing κ selectivity.
Copyright © 2010 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Analgesics / chemical synthesis*
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Analgesics / chemistry
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Analgesics / metabolism
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Analgesics / pharmacology*
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Animals
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Benzamides / chemistry
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Benzamides / pharmacology
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Drug Design
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Epoxy Compounds / chemical synthesis*
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Epoxy Compounds / chemistry
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Epoxy Compounds / metabolism
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Epoxy Compounds / pharmacology*
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Male
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Mice
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Molecular Structure
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Molecular Targeted Therapy
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Morphinans / chemical synthesis*
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Morphinans / chemistry
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Morphinans / metabolism
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Morphinans / pharmacology*
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Receptors, Opioid
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Receptors, Opioid, kappa / agonists*
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Receptors, Opioid, kappa / metabolism
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Structure-Activity Relationship
Substances
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Analgesics
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Benzamides
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Epoxy Compounds
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Morphinans
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NS22 compound
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Receptors, Opioid
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Receptors, Opioid, kappa