TY - CHAP
T1 - SLC6 neurotransmitter transporter family
AU - Alexander, Stephen P.H.
AU - Benson, Helen E.
AU - Faccenda, Elena
AU - Pawson, Adam J.
AU - Sharman, Joanna L.
AU - CmGrath, John C.
AU - Catterall, William A.
AU - Spedding, Michael
AU - Peters, John A.
AU - Harmar, Anthony J.
AU - Broer, Stefan
PY - 2013
Y1 - 2013
N2 - 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.
AB - 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.
KW - adiponectin receptor 1
KW - amino acid transporter
KW - catalytic receptor
KW - cellular retinoic acid binding protein 1
KW - cellular retinoic acid binding protein 2
KW - enzyme
KW - fatty acid binding protein
KW - fatty acid binding protein 1
KW - fatty acid binding protein 2
KW - fatty a
M3 - Entry for encyclopedia/dictionary
VL - 170
SP - 1728
EP - 1731
BT - The Concise Guide to PHARMACOLOGY 2013/14: Overview
PB - Wiley Online Library
CY - London UK
ER -