The Concise Guide to PHARMACOLOGY 2013/14: ion channels
- PMID: 24528239
- PMCID: PMC3892289
- DOI: 10.1111/bph.12447
The Concise Guide to PHARMACOLOGY 2013/14: ion channels
Abstract
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. The full contents can be found at http://onlinelibrary.wiley.com/doi/10.1111/bph.12444/full. Ion channels are one of the seven major pharmacological targets into which the Guide is divided, with the others being G protein-coupled receptors, ligand-gated 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 and 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 the Guide to Receptors and Channels, providing a permanent, citable, point-in-time record that will survive database updates.
Copyright © 2013 The British Pharmacological Society.
References
Further reading
-
- Doyle D. Morais Cabral J. Pfuetzner RA. Kuo A. Gulbis JM. Cohen SL. Chait B. MacKinnon R. The structure of the potassium channel : molecular basis of potassium conduction and selectivity. Science. 1998;280:69–77. - PubMed
-
- Dunlop J. Bowlby M. Peri R. Vasilyev D. Arias R. High-throughput electrophysiology: an emerging paradigm for ion channel screening and physiology. Nat Rev Drug Discov. 2008;7:358–368. - PubMed
-
- Dutzler R. Campbell EB. Cadene M. Chait B. MacKinnon R. X-ray structure of a ClC chloride channel at 3.0A reveals the molecular basis of ion selectivity. Nature. 2002;415:287–294. - PubMed
-
- Hille B. 3rd Edition. Sunderland MA: Sinauer Associates; 2006. Ion channel of excitable membranes.
-
- Overington JP. Al-Lazikani B. Hopkins AL. Nat Rev Drug Discov. Vol. 5. 2001. How many drug targets are there? pp. 993–996. - PubMed
References
-
- Akopian AN, et al. Neuroreport. 2000;11:2217–2222. [PMID: 10923674 ] - PubMed
-
- Andrey F, et al. Biochim Biophys Acta. 2005;1745:1–6. [PMID: 16085050 ] - PubMed
-
- Babinski K, et al. J Biol Chem. 2000;275:28519–28525. [PMID: 10842183 ] - PubMed
-
- Babinski K, et al. J Neurochem. 1999;72:51–57. [PMID: 9886053 ] - PubMed
-
- Baron A, et al. J Biol Chem. 2001;276:35361–35367. [PMID: 11457851 ] - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous