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Titlebook: endoCANNABINOIDS; Actions at Non-CB1/C Mary E. Abood,Roger G Sorensen,Nephi Stella Book 2013 Springer Science+Business Media New York 2013

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书目名称endoCANNABINOIDS
副标题Actions at Non-CB1/C
编辑Mary E. Abood,Roger G Sorensen,Nephi Stella
视频video
概述Research provided by leading scientists.Complement recent texts that describe cannabinoids, the endocannabinoid system, the physiological roles of cannabinoids as mediated through their actions at can
丛书名称The Receptors
图书封面Titlebook: endoCANNABINOIDS; Actions at Non-CB1/C Mary E. Abood,Roger G Sorensen,Nephi Stella Book 2013 Springer Science+Business Media New York 2013
描述This book is intended as a scientific resource for cannabinoid researchers carrying out animal and human experiments, and for those who are interested in learning about future directions in cannabinoid research. Additionally, this book may be of value to investigators currently working outside the field of cannabinoid research who have an interest in learning about these compounds and their atypical cannabinoid signalling. This book provides insight into the potential medical application of cannabinoids and their therapeutic development for the treatment of human disease.
出版日期Book 2013
关键词animal research; atypical endocannabinoid actions; atypical endocannabinoid receptors; cannabinoids; end
版次1
doihttps://doi.org/10.1007/978-1-4614-4669-9
isbn_softcover978-1-4899-8846-1
isbn_ebook978-1-4614-4669-9Series ISSN 1048-6909 Series E-ISSN 2524-6488
issn_series 1048-6909
copyrightSpringer Science+Business Media New York 2013
The information of publication is updating

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GPR18 and NAGly Signaling: New Members of the Endocannabinoid Family or Distant Cousins?C) and .arachidonoyl glycine (NAGly) by an oxygenated metabolite of the endogenous cannabinoid anandamide (AEA). The review will outline what is known about this receptor, the ligands that activate and block the receptor, and how these interactions fit within cannabinoid/endocannabinoid signaling.
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978-1-4899-8846-1Springer Science+Business Media New York 2013
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Nanostructure Science and Technologyptors, G protein-coupled receptors (GPCRs) identified by molecular cloning in the early 1990s. Since that time, there has been a growing body of pharmacological evidence indicating the existence of additional molecular targets for cannabinoids. This chapter overviews the nonclassical targets thought
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https://doi.org/10.1007/978-94-011-2538-3ein-coupled receptors (GPCRs) that bind constituents of ., such as the classical cannabinoid agonist (−)-.-delta-9-tetrahydrocannabinol [(−)-Δ.-THC (.)]. CB.R and CB.R bind four other structural classes of ligands (see Fig. 2.1): nonclassical cannabinoid agonists typified by 2-[5-Hydroxy-2-(3-hydrox
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