| 書目名稱 | Functional Selectivity of G Protein-Coupled Receptor Ligands |
| 副標題 | New Opportunities fo |
| 編輯 | Kim A. Neve |
| 視頻video | http://file.papertrans.cn/350/349810/349810.mp4 |
| 概述 | Includes supplementary material: |
| 叢書名稱 | The Receptors |
| 圖書封面 |  |
| 描述 | .Functional selectivity refers to the ability of different ligands acting at one receptor subtype to activate multiple signaling pathways in unique combinations; that is, one drug can be an agonist at pathway A and an antagonist or partial agonist at pathway B, and another drug can have the reverse profile. Functional selectivity has profound implications for drug development, for chemical biology, and for the design of experiments to characterize receptor function. In Functional Selectivity of G Protein-Coupled Receptors expert neuroscientists and pharmacologists review the work that demonstrated the existence of functional selectivity, placed it within a theoretical framework, and provided a mechanistic basis for the phenomenon. This exciting, comprehensive, and future-oriented volume includes chapters that focus on theoretical and mechanistic aspects of functional selectivity and that cut across subfamilies of GPCRs. Additional chapters focus on subfamilies of therapeutically relevant receptors where there is considerable evidence of ligand functional selectivity. Accessible and authoritative, Functional Selectivity of G Protein-Coupled Receptors is a valuable educational tool a |
| 出版日期 | Book 2009 |
| 關(guān)鍵詞 | biology; cannabinoid; dopamine; drug; drug development; drug discovery; lipide; opioid; receptor; serotonin |
| 版次 | 1 |
| doi | https://doi.org/10.1007/978-1-60327-335-0 |
| isbn_softcover | 978-1-4939-6116-0 |
| isbn_ebook | 978-1-60327-335-0Series ISSN 1048-6909 Series E-ISSN 2524-6488 |
| issn_series | 1048-6909 |
| copyright | The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Busines |
|Archiver|手機版|小黑屋|
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