Functional Selectivity of G Protein-Coupled Receptor Ligands : New Opportunities for Drug Discovery

Language: English

Published by Humana Press Mär 2009, 2009

1603273344 / 9781603273343

Series: Book 5 of 29 - The Receptors

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Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH

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Neuware - 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 and reference source for students and scientists interested in drug development, chemical biology, and GPCR function.

Seller Inventory # 9781603273343

Title
Functional Selectivity of G Protein-Coupled Receptor Ligands : New Opportunities for Drug Discovery
Author
Kim Neve
Publisher
Humana Press Mär 2009
Publication year
2009
Condition
Neu
Binding
Buch
Language
English
ISBN 10
1603273344
ISBN 13
9781603273343
Item weight
570 grams
Dimensions
241x161x20 mm
Series
Book 5 of 29: The Receptors

AHA-BUCH GmbH

Einbeck, Germany

5-star seller

AbeBooks seller since August 14, 2006

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