Identification of Binding Sites for Calcium Channel Antagonists
スポンサーリンク
概要
- 論文の詳細を見る
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.
- International Heart Journal刊行会の論文
著者
-
Nakayama Hitoshi
Faculty of Pharmaceutical Sciences, Kumamoto University
-
Kuniyasu Akihiko
Faculty Of Pharmaceutical Sciences Kumamoto University
-
Nakayama Hitoshi
Faculty Of Pharmaceutical Sciences Hokkaido University
関連論文
- -P611- CHINESE SCORPION TOXIN ACTIVATES THE RYANODINE RECEPTOR Ca^ RELEASE CHANNELS.(PROCEEDINGS OF THE 59th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY)
- 3-Benzyl-5-(4-hydroxyphenyl)-2-[4-(1-azi-2,2,2-trifluoroethyl)phenylacetamido]pyrazine, a Photoreactive Analogue of Coelenteramid. Synthesis and Photolysis
- Cardiac Glycosides from Erysimum cheiranthoides
- Modulation of synaptic transmission in hippocampal CA1 neurons by a novel neurotoxin (β-pompilidotoxin) derived from wasp venom
- Identification of Binding Sites for Calcium Channel Antagonists