Discovery, Synthesis, and Molecular Pharmacology of Selective Positive Allosteric Modulators of the δ-Opioid Receptor

Allosteric modulators of G protein-coupled receptors (GPCRs) have a number of potential advantages compared to agonists or antagonists that bind to the orthosteric site of the receptor. These include the potential or receptor selectivity, maintenance of the temporal and spatial fidelity of signaling...

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Vydáno v:J Med Chem
Hlavní autoři: Burford, Neil T., Livingston, Kathryn E., Canals, Meritxell, Ryan, Molly R., Budenholzer, Lauren M. L., Han, Ying, Shang, Yi, Herbst, John J., O'Connell, Jonathan, Banks, Martyn, Zhang, Litao, Filizola, Marta, Bassoni, Daniel L., Wehrman, Tom S., Christopoulos, Arthur, Traynor, John R., Gerritz, Samuel W., Alt, Andrew
Médium: Artigo
Jazyk:Inglês
Vydáno: 2015
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4703104/
https://ncbi.nlm.nih.gov/pubmed/25901762
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.jmedchem.5b00007
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