Abstract
The pharmacological activity of rigid analogues of 1,4-dihydropyridine calcium entry antagonists 9-16 is demonstrated by dose-dependent inhibition of the calcium contraction in depolarized rat aortic strips and by a [3H]nitrendipine binding assay in using cardiac sarcolemmal membranes. From the results, a model is proposed as the receptor-bound conformation of the dihydropyridine calcium entry antagonists.
MeSH terms
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Animals
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Aorta / drug effects
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Calcium Channel Blockers / pharmacology*
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Chemical Phenomena
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Chemistry
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Dihydropyridines*
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Dose-Response Relationship, Drug
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Heterocyclic Compounds / pharmacology*
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Ion Channels / drug effects
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Male
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Nitrendipine / metabolism
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Protein Binding / drug effects
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Pyridines / pharmacology
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Rats
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Rats, Inbred Strains
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Sarcolemma / drug effects
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Sarcolemma / metabolism
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Structure-Activity Relationship
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Swine
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Terpenes / pharmacology
Substances
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Calcium Channel Blockers
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Dihydropyridines
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Heterocyclic Compounds
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Ion Channels
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Pyridines
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Terpenes
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1,4-dihydropyridine
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Nitrendipine