Alexander Stephen P H, Benson Helen E, Faccenda Elena, Pawson Adam J, Sharman Joanna L, McGrath John C, Catterall William A, Spedding Michael, Peters John A, Harmar Anthony J, Abul-Hasn N, Anderson C M, Anderson C M H, Araiksinen M S, Arita M, Arthofer E, Barker E L, Barratt C, Barnes N M, Bathgate R, Beart P M, Belelli D, Bennett A J, Birdsall N J M, Boison D, Bonner T I, Brailsford L, Bröer S, Brown P, Calo G, Carter W G, Catterall W A, Chan S L F, Chao M V, Chiang N, Christopoulos A, Chun J J, Cidlowski J, Clapham D E, Cockcroft S, Connor M A, Cox H M, Cuthbert A, Dautzenberg F M, Davenport A P, Dawson P A, Dent G, Dijksterhuis J P, Dollery C T, Dolphin A C, Donowitz M, Dubocovich M L, Eiden L, Eidne K, Evans B A, Fabbro D, Fahlke C, Farndale R, Fitzgerald G A, Fong T M, Fowler C J, Fry J R, Funk C D, Futerman A H, Ganapathy V, Gaisnier B, Gershengorn M A, Goldin A, Goldman I D, Gundlach A L, Hagenbuch B, Hales T G, Hammond J R, Hamon M, Hancox J C, Hauger R L, Hay D L, Hobbs A J, Hollenberg M D, Holliday N D, Hoyer D, Hynes N A, Inui K-I, Ishii S, Jacobson K A, Jarvis G E, Jarvis M F, Jensen R, Jones C E, Jones R L, Kaibuchi K, Kanai Y, Kennedy C, Kerr I D, Khan A A, Klienz M J, Kukkonen J P, Lapoint J Y, Leurs R, Lingueglia E, Lippiat J, Lolait S J, Lummis S C R, Lynch J W, MacEwan D, Maguire J J, Marshall I L, May J M, McArdle C A, McGrath J C, Michel M C, Millar N S, Miller L J, Mitolo V, Monk P N, Moore P K, Moorhouse A J, Mouillac B, Murphy P M, Neubig R R, Neumaier J, Niesler B, Obaidat A, Offermanns S, Ohlstein E, Panaro M A, Parsons S, Pwrtwee R G, Petersen J, Pin J-P, Poyner D R, Prigent S, Prossnitz E R, Pyne N J, Pyne S, Quigley J G, Ramachandran R, Richelson E L, Roberts R E, Roskoski R, Ross R A, Roth M, Rudnick G, Ryan R M, Said S I, Schild L, Sanger G J, Scholich K, Schousboe A, Schulte G, Schulz S, Serhan C N, Sexton P M, Sibley D R, Siegel J M, Singh G, Sitsapesan R, Smart T G, Smith D M, Soga T, Stahl A, Stewart G, Stoddart L A, Summers R J, Thorens B, Thwaites D T, Toll L, Traynor J R, Usdin T B, Vandenberg R J, Villalon C, Vore M, Waldman S A, Ward D T, Willars G B, Wonnacott S J, Wright E, Ye R D, Yonezawa A, Zimmermann M
School of Life Sciences, University of Nottingham Medical School, Nottingham, NG7 2UH, UK.
Br J Pharmacol. 2013 Dec;170(8):1449-58. doi: 10.1111/bph.12444.
The Concise Guide to PHARMACOLOGY 2013/14 provides concise overviews of the key properties of over 2000 human drug targets with their pharmacology, 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 from the IUPHAR database. The full contents can be found at http://onlinelibrary.wiley.com/doi/10.1111/bph.12444/full. This compilation of the major pharmacological targets is divided into seven areas of focus: G protein-coupled receptors, ligand-gated ion channels, ion channels, catalytic receptors, nuclear hormone receptors, transporters and enzymes. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. A new landscape format has easy to use tables comparing related targets. It is a condensed version of material contemporary to late 2013, which is presented in greater detail and constantly updated on the website www.guidetopharmacology.org, superseding data presented in previous Guides to Receptors & Channels. It is produced in conjunction with NC-IUPHAR and provides the official IUPHAR classification and nomenclature for human drug targets, where appropriate. It consolidates information previously curated and displayed separately in IUPHAR-DB and GRAC and provides a permanent, citable, point-in-time record that will survive database updates.
《2013/14药理学简明指南》简要概述了2000多种人类药物靶点的关键特性及其药理学,还提供了药物靶点及其配体开放获取知识库(www.guidetopharmacology.org)的链接,该知识库提供了来自IUPHAR数据库的靶点和配体特性的更详细信息。完整内容可在http://onlinelibrary.wiley.com/doi/10.1111/bph.12444/full查询。这份主要药理学靶点的汇编分为七个重点领域:G蛋白偶联受体、配体门控离子通道、离子通道、催化受体、核激素受体、转运体和酶。书中给出了命名指导以及关于最佳可用药理学工具的总结信息,同时列出了关键参考文献和进一步阅读建议。一种新的页面格式有便于使用的表格来比较相关靶点。它是2013年末当代资料的精简版,在网站www.guidetopharmacology.org上有更详细的呈现且不断更新,取代了之前《受体与通道指南》中的数据。它是与NC - IUPHAR联合制作的,在适当情况下提供人类药物靶点的官方IUPHAR分类和命名。它整合了之前在IUPHAR - DB和GRAC中分别整理和展示的信息,并提供了一份永久性的、可引用的、特定时间点的记录,该记录在数据库更新后依然存在。