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本文引用的文献

1
Involvement of the calcium-sensing receptor in human taste perception.钙敏感受体在人类味觉感知中的作用。
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2
Clinical use of GnRH analogues.促性腺激素释放激素类似物的临床应用。
Clin Endocrinol (Oxf). 2002 Jun;56(6):677-87. doi: 10.1046/j.1365-2265.2002.01291.x.
3
Subtype-specific stimulation of [35S]GTPgammaS binding by recombinant alpha2-adrenoceptors.重组α2肾上腺素能受体对[35S]GTPγS结合的亚型特异性刺激作用。
Eur J Pharmacol. 1998 Aug 21;355(2-3):275-9. doi: 10.1016/s0014-2999(98)00518-4.
4
The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency.一系列新型含(喹啉-2-基甲氧基)苯基化合物作为高亲和力白三烯受体拮抗剂的研发。3. 酸性侧链的结构变化以获得效力增强的拮抗剂。
J Med Chem. 1990 Oct;33(10):2828-41. doi: 10.1021/jm00172a024.

《药理学 2017/18 简明指南:G 蛋白偶联受体》

THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: G protein-coupled receptors.

机构信息

School of Life Sciences, University of Nottingham Medical School, Nottingham, NG7 2UH, UK.

Monash Institute of Pharmaceutical Sciences and Department of Pharmacology, Monash University, Parkville, Victoria 3052, Australia.

出版信息

Br J Pharmacol. 2017 Dec;174 Suppl 1(Suppl Suppl 1):S17-S129. doi: 10.1111/bph.13878.

DOI:10.1111/bph.13878
PMID:29055040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5650667/
Abstract

The Concise Guide to PHARMACOLOGY 2017/18 provides concise overviews of the key properties of nearly 1800 human drug targets with an emphasis on selective pharmacology (where available), plus links to an open access knowledgebase of drug targets and their ligands (www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide represents approximately 400 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/10.1111/bph.13878/full. G protein-coupled receptors are one of the eight major pharmacological targets into which the Guide is divided, with the others being: ligand-gated ion channels, voltage-gated ion channels, other ion channels, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2017, and supersedes data presented in the 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature Committee of the Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate.

摘要

《药理学概要 2017/18》提供了近 1800 个人类药物靶点的关键特性的简明概述,重点是选择性药理学(如适用),并链接到药物靶点及其配体的开放获取知识库(www.guidetopharmacology.org),其中提供了更详细的靶点和配体特性视图。尽管《药理学概要》约有 400 页,但与网站上呈现的信息和链接相比,所呈现的内容大大减少。它提供了一个永久的、可引用的、时间点记录,将在数据库更新后保留。这一部分的全部内容可在 http://onlinelibrary.wiley.com/doi/10.1111/bph.13878/full 找到。G 蛋白偶联受体是该指南分为的八个主要药理学靶点之一,其他靶点包括:配体门控离子通道、电压门控离子通道、其他离子通道、核激素受体、催化受体、酶和转运体。这些靶点都有命名指南和最佳可用药理学工具的摘要信息,以及关键参考文献和进一步阅读的建议。《药理学概要》的全景格式旨在促进与 2017 年年中相关靶点的比较,并取代了 2015/16 年和 2013/14 年《药理学概要》以及之前的《受体和通道指南》中呈现的数据。它是与基础和临床药理学联合会命名委员会(NC-IUPHAR)密切合作编写的,因此,在适当情况下,为人类药物靶点提供了官方的 IUPHAR 分类和命名。