Abstract
A series of 26 derivatives of the novel muscarinic antagonist 3-(2-benzofuranyl)quinuclidin-2-ene (1) has been synthesized and evaluated for muscarinic and antimuscarinic properties. The affinity of the compounds was determined by competition experiments in homogenates of cerebral cortex, heart, parotid gland, and urinary bladder from guinea pigs using (-)-[3H]-3-quinuclidinyl benzilate as the radioligand, and the antimuscarinic-potency was determined in a functional assay on isolated guinea pig urinary bladder using carbachol as the agonist. The 5-fluorobenzofuranyl derivative was slightly more potent than 1. The 7-bromo-substituted 8 displayed a 14-fold tissue selectivity ratio for muscarinic receptors in the cortex versus the parotid gland. Comparative molecular field analysis and quantitative structure-activity relationship models were developed for this series of substituted benzofuranyl derivatives.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Benzofurans / chemical synthesis*
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Benzofurans / chemistry
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Benzofurans / pharmacology
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Binding, Competitive
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Cerebral Cortex / metabolism
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Cholinergic Agents / chemistry*
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Cholinergic Agents / pharmacology
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Guinea Pigs
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In Vitro Techniques
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Kinetics
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Male
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Models, Molecular
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Molecular Sequence Data
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Molecular Structure
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Muscarinic Antagonists / chemical synthesis*
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Muscarinic Antagonists / chemistry
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Muscarinic Antagonists / pharmacology
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Muscle, Smooth / drug effects
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Muscle, Smooth / physiology
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Organ Specificity
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Protein Conformation
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Quinuclidines / chemical synthesis*
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Quinuclidines / chemistry
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Quinuclidines / pharmacology
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Quinuclidinyl Benzilate / metabolism
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Radioligand Assay
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Receptors, Muscarinic / drug effects
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Receptors, Muscarinic / physiology*
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Structure-Activity Relationship
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Urinary Bladder / drug effects
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Urinary Bladder / physiology
Substances
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Benzofurans
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Cholinergic Agents
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Muscarinic Antagonists
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Quinuclidines
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Receptors, Muscarinic
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Quinuclidinyl Benzilate