Beschreibung:
Edited by the most prominent person in the field and top researchers at US pharmaceutical companies, this is a unique resource for drug developers and physiologists seeking a molecular-level understanding of ion channel pharmacology. After an introduction to the topic, the authors evaluate the structure and function of ion channels, as well as related drug interaction. A section on assay technologies is followed by a section each on calcium, sodium and potassium channels. Further chapters cover genetic and acquired channelopathies, before the book closes with a look at safety issues in ion channel drug development. For medicinal and pharmaceutical chemists, biochemists, molecular biologists and those working in the pharmaceutical industry.
Edited by the most prominent person in the field and top researchers at US pharmaceutical companies, this is a unique resource for drug developers and physiologists seeking a molecular-level understanding of ion channel pharmacology.After an introduction to the topic, the authors evaluate the structure and function of ion channels, as well as related drug interaction. A section on assay technologies is followed by a section each on calcium, sodium and potassium channels. Further chapters cover genetic and acquired channelopathies, before the book closes with a look at safety issues in ion channel drug development.For medicinal and pharmaceutical chemists, biochemists, molecular biologists and those working in the pharmaceutical industry.
IntroductionStructure and Function of Ion ChannelsDrug Interaction at Ion ChannelsAssay TechnologiesBinding StudiesIon FluxesFluorescence StudiesPatch ClampingCalcium ChannelsOverviewT-type ChannelsL-type ChannelsN-type ChannelsSodium ChannelsOverviewChannel Subtype SelectivityPotassium ChannelsOverviewKv1.3Kv1.5Ca-activated channelsK(ATP)KCNQGenetic and Acquired ChannelopathiesOverviewHERGLong QT SyndromeSafety Issues in Ion Channel Drug Development