Description
Pharmacology of G Protein Coupled Receptors
Author: ENNA S. J.
Language: EnglishSubject for Pharmacology of G Protein Coupled Receptors:
Keywords
allosteric modulator; arrestin; biosynthesis; bone remodeling; calcium-sensing receptor; cancer; cannabinoid; cell signaling; CNS; cotranslational regulation; desensitization; drug discovery; endoplasmic reticulum quality control; FFA1; FFA2; FFA3; free fatty acid; functional selectivity; G protein-coupled receptor; G protein-coupled receptors; gonadotropin-releasing hormone; gonadotropin-releasing hormone receptor; GPR109A; GPR109B; GPR120; GPR55; GPR81; GPR84; hydroxy-carboxylic acid receptors; inflammation; LPI; membrane protein biosynthesis; metabotropic glutamate receptor; mutant rescue; NAM; neuromodulation; nicotinic acid; PAM; parathyroid hormone; PDZ proteins; pharmacologic chaperones; pharmacoperones; posttranslational modification; protein complexes; protein misfolding; protein-protein interactions; receptor endocytosis; receptor trafficking; recycling; RGS proteins; signaling; structure-based drug discovery; type 1 parathyroid hormone receptor
408 p. · 15x22.8 cm · Hardback
Out of Print
Description
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G protein coupled receptors remain the most important class of therapeutic targets in medicine. In the last 5 years, tremendous advances have been made in our understanding of the structure and mechanism of this critical family of drug targets. The present volume explores the modern experimental and conceptual framework for drug discovery for G protein coupled receptors. It explores advances in structure determination and structure-based drug design as well as new concepts of allosteric modulation, functional selectivity/biased agonism, and pharmacological chaperones. In addition, emerging drug targets such as receptor families for fatty acids, carboxylic acids, lipid mediators, etc. are included. Final chapters cover novel mechanisms of signal regulation through PDZ domains and RGS proteins. This volume will bring an up-to-date perspective on the G protein coupled receptor field to both academic and industry scientists.
- The Use of GPCR Structures in Drug Design Miles Congreve, Christopher Langmead and Fiona Marshall
- Allosteric Modulation of Metabotropic Glutamate Recetors Douglas J. Sheffler, Karen J. Gregory, Jerri M. Rook, and P. Jeffrey Conn
- Refining Efficacy: Exploiting Functional Selectivity for Drug Discovery Diane Gesty-Palmer and Louis M. Luttrell
- Pharmacoperones for Misfolded Gonadotropin – Releasing Hormone Receptors P. Michael Conn and Alfredo Ulloa-Aguirre
- Regulation of Stability and Trafficking of Calcium Sensing Receptors by Pharmacologic Chaperones Ying Huang, Alice Cavanaugh, and Gerda E. Breitwieser
- Experimental Challenges to Targeting Poorly Characterised GPCRs: Therapeutic Potential for Free Fatty Acid Receptor Brian D. Hudson, Nicola J. Smith and Graeme Milligan
- Biological and Pharmacological Roles of HCA Receptors Clara Blad, Kashan Ahmed, Ad IJzerman, and Stefan Offermanns
- Pharmacology, Signaling and Physiological Relevance of the G Protein-Coupled Receptor 55 (GPR55) Nariman Balenga, Julia Kargl and Maria Waldhoer
- Role of PDZ Proteins in Regulating Signaling, Trafficking, and Function of GPCRs Paul Temkin, Mark von Zastrow, Peter A. Friedman, and Guillermo Romero
- Regulator of G Protein Signaling Proteins as Drug Targets: Current State and Future Possibilities Benita Sjögren
- GPCR-Interacting Proteins, Major Players in GPCR Function Pascal Maurice, Maud Kamal, Avais Daulat, Jean-Luc Guillaume, and Ralf Jockers
Pharmacologists, immunologists, and biochemists
- The present volume explores the modern experimental and conceptual framework for drug discovery for G protein coupled receptors
- It explores advances in structure determination and structure-based drug design as well as new concepts of allosteric modulation, functional selectivity/biased agonism, and pharmacological chaperones
- This volume will bring an up-to-date perspective on the G protein coupled receptor field to both academic and industry scientists
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