Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/9547
Title: Calcium channels and their involvement in cardiovascular disease.
Authors: Nayler, W G
Affiliation: Department of Medicine, University of Melbourne, Austin Hospital, Heidelberg, Victoria, Australia.
Issue Date: 9-Jan-1992
Citation: Biochemical Pharmacology; 43(1): 39-46
Abstract: The widespread distribution of L-type Ca2+ channels in the cardiovascular system makes that system a natural 'target' for drugs which inhibit L-type Ca2+ channel activity. Now that tissue-dependent differences in the chemical composition of the calcium antagonist binding sites have been recognized it may be possible to develop drugs with enhanced tissue selectivity. The search for new compounds should not be restricted to improvements in tissue selectivity, however. Some of the ancillary properties of the L-type Ca2+ channel inhibitors--including their ability to protect against lipid peroxidation--should not be lost because these ancillary properties may contribute significantly to their usefulness as therapeutic agents.
Internal ID Number: 1310407
URI: http://ahro.austin.org.au/austinjspui/handle/1/9547
URL: http://www.ncbi.nlm.nih.gov/pubmed/1310407
Type: Journal Article
Subjects: Binding Sites
Brain Ischemia.metabolism
Calcium Channel Blockers.metabolism
Calcium Channels.metabolism
Cardiovascular Diseases.drug therapy.metabolism
Drug Design
Humans
Appears in Collections:Journal articles

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