The binding of naproxen, ketoprofen, phenylbutazone, salicylic acid, azapropazone, and indobufen to bovine serum albumin was studied by applying the potentiometric ion probe technique. An ion-selective electrode for the ion probe 1-anilino-8-naphthalene-sulfonate was utilized for the purposes of thi
โฆ LIBER โฆ
Ion channels as pharmacologic receptors: The chirality of drug interactions
โ 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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โฆ 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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๐
English
โ 610 KB