Abstract
The binding sites of three typical calcium channel antagonists, 1, 4-dihydropyridines, benzothiazepines and phenylalkylamines, were successfully identified within the primary structures of calcium channels using a photoaffinity labeling technique. The results confirm pharmacological observations of the three antagonists that had been proposed to interact allosterically with each other. We briefly review the results and discuss the future prospects.
MeSH terms
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Affinity Labels
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Benzazepines / metabolism
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Binding Sites
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Calcium Channel Blockers / chemistry*
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Calcium Channel Blockers / metabolism*
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Calcium Channel Blockers / pharmacology
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Calcium Channels / metabolism*
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Dihydropyridines / metabolism
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Diltiazem / metabolism
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Drug Interactions
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Humans
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Muscle, Skeletal / metabolism*
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Thiazepines / metabolism
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Verapamil / analogs & derivatives
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Verapamil / metabolism
Substances
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Affinity Labels
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Benzazepines
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Calcium Channel Blockers
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Calcium Channels
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Dihydropyridines
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Thiazepines
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1,4-dihydropyridine
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Verapamil
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Diltiazem