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Ion channels as pharmacologic receptors: The chirality of drug interactions

โœ Scribed by David J. Triggle


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
347 KB
Volume
8
Category
Article
ISSN
0899-0042

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โœฆ Synopsis


Ion channels are pharmocologic receptors and as such exhibit stereoselective interactions with drugs. Ion channels are conformationally mobile transmembrane proteins existing in a number of open and closed states. Drug interactions with these Merent states may differ quantitatively and qualitatively. Stereoselectivity may not be a constant factor and may change according to channel state as determined by stimulus mode or experimental conditions. Selected examples are cited for Na+ and Ca2+ channels.


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