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Neuropharmacology, ISSN 0028-3908, 05/2016, Volume 104, pp. 31 - 49
Pharmacological tool compounds are now available to define action at the adenosine (ARs), P2Y and P2X receptors. We present a selection of the most commonly... 
Nucleosides | GPCR | Agonists | Antagonists | Nucleotides | Ion channel | ATP | PROTEIN-COUPLED RECEPTORS | ALLOSTERIC MODULATION | NEUROSCIENCES | NEUROPATHIC PAIN | NUCLEOTIDE PYROPHOSPHATASE/PHOSPHODIESTERASE | IN-VIVO | ION-CHANNEL | PHARMACOLOGY & PHARMACY | CENTRAL-NERVOUS-SYSTEM | PURINERGIC RECEPTOR | P2Y RECEPTOR | STRUCTURE-BASED DESIGN | Purinergic P1 Receptor Agonists - chemistry | Receptors, Purinergic P2Y - chemistry | Receptors, Purinergic P2X - chemistry | Humans | Purinergic P1 Receptor Agonists - pharmacology | Receptors, Purinergic P2Y - metabolism | Purinergic P1 Receptor Antagonists - therapeutic use | Purinergic P2Y Receptor Agonists - chemistry | Purinergic P2Y Receptor Agonists - therapeutic use | Structure-Activity Relationship | Purinergic P1 Receptor Agonists - therapeutic use | Chemistry, Pharmaceutical | Purinergic P1 Receptor Antagonists - pharmacology | Purinergic P2Y Receptor Agonists - pharmacology | Receptors, Purinergic P1 - chemistry | Animals | Purinergic Agents - chemistry | Purinergic Agents - therapeutic use | Receptors, Purinergic P2X - metabolism | Receptors, Purinergic P1 - metabolism | Purinergic Agents - pharmacology | Purinergic P1 Receptor Antagonists - chemistry | Prevention | Brain | Purines | Enzymes | Injuries | Chronic pain | Cancer | antagonists | nucleosides | agonists | ion channel | nucleotides
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 01/2015, Volume 89, pp. 561 - 580
The purinergic P2X receptors are ligand-gated cation channels activated by the endogenous ligand ATP. They assemble as homo- or heterotrimers from seven cloned... 
Molecular modelling | Nucleotides | Purinergic receptors | P2X receptor antagonists | P2X receptor agonists | P2X receptors | POTENT ANTAGONIST | SURAMIN ANALOG NF279 | CHEMISTRY, MEDICINAL | PHARMACOLOGICAL CHARACTERIZATION | AGONIST BINDING | ATP-BINDING | EXTRACELLULAR LOOP | NEUROPATHIC PAIN | CONFORMATIONAL ENERGIES | MOLECULAR-FORCE FIELD | IN-VITRO ACTIVITY | Anthraquinones - metabolism | Receptors, Purinergic P2X - chemistry | Humans | Molecular Conformation | Azoles - metabolism | Guanidines - pharmacology | Purinergic P2X Receptor Agonists - metabolism | Purinergic P2X Receptor Antagonists - pharmacology | Structure-Activity Relationship | Adenosine Triphosphate - metabolism | Purinergic P2X Receptor Agonists - chemistry | Receptors, Purinergic P2X - metabolism | Binding Sites | Guanidines - metabolism | Polycyclic Compounds - metabolism | Phenols - pharmacology | Polycyclic Compounds - chemistry | Models, Molecular | Rats | Zebrafish | Phenols - metabolism | Azoles - pharmacology | Purinergic P2X Receptor Agonists - pharmacology | Azoles - chemistry | Guanidines - chemistry | Polycyclic Compounds - pharmacology | Animals | Purinergic P2X Receptor Antagonists - chemistry | Purinergic P2X Receptor Antagonists - metabolism | Ligands | Phenols - chemistry | Anthraquinones - pharmacology | Anthraquinones - chemistry | Structure | Analysis | Crystals | Membrane proteins | Index Medicus
Journal Article
2011, ISBN 9780123855268, Volume 61
Seven P2X receptor subunits have been cloned which form functional homo- and heterotrimers. These are cation-selective channels, equally permeable to Na and K... 
pain | cancer | CNS disorders | neurotransmission | purinergic | ATP | Purinergic | Pain | Neurotransmission | Cancer | Animals | Disease | Health | Models, Biological | Receptors, Purinergic P2X - chemistry | Humans | Models, Molecular | Receptors, Purinergic P2X - metabolism
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