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《药理学 2017/18 简明指南:电压门控离子通道》

THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Voltage-gated ion channels.

机构信息

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

Pharmacology and Toxicology, Institute of Pharmacy, University of Innsbruck, A-6020, Innsbruck, Austria.

出版信息

Br J Pharmacol. 2017 Dec;174 Suppl 1(Suppl Suppl 1):S160-S194. doi: 10.1111/bph.13884.

DOI:10.1111/bph.13884
PMID:29055033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5650668/
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.13884/full. Voltage-gated ion channels are one of the eight major pharmacological targets into which the Guide is divided, with the others being: G protein-coupled receptors, ligand-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,呈现的内容大大减少。它提供了一个永久性的、可引用的、时点记录,将在数据库更新后保留。本节的全部内容可在 http://onlinelibrary.wiley.com/doi/10.1111/bph.13884/full 找到。电压门控离子通道是指南分为的八个主要药理学靶点之一,其他靶点包括:G 蛋白偶联受体、配体门控离子通道、其他离子通道、核激素受体、催化受体、酶和转运体。这些靶点都提供了命名指导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建议。《药理学概要》的全景格式旨在促进对 2017 年年中相关靶点的比较,并取代 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,在适当的情况下,为人类药物靶点提供了官方的 IUPHAR 分类和命名。