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Bioorganic & Medicinal Chemistry Letters|October 10, 2002
New irreversible adenosine A(1) antagonists based on FSCPXAnthony R Beauglehole, Stephen P Baker, Peter J ScammellsChemmedchem|October 10, 2013
Effect of linker length and composition on heterobivalent ligand-mediated receptor cross-talk between the A1 adenosine and β2 adrenergic receptorsNicholas Barlow, Stephen P Baker, Peter J ScammellsBioorganic & Medicinal Chemistry|February 12, 2002
New 2,N6-disubstituted adenosines: potent and selective A1 adenosine receptor agonistsSally A Hutchinson, Stephen P Baker, Peter J ScammellsJournal of Medicinal Chemistry|September 12, 2008
Synthesis of bivalent beta2-adrenergic and adenosine A1 receptor ligandsPeter Karellas, Michael McNaughton, Stephen P Baker, et al.Bioorganic & Medicinal Chemistry|September 1, 2004
New potent and selective A1 adenosine receptor agonistsSally A Hutchinson, Stephen P Baker, Joel Linden, et al.Bioorganic & Medicinal Chemistry|November 29, 2007
N6-substituted C5'-modified adenosines as A1 adenosine receptor agonistsT D Ashton, Stephen P Baker, Sally A Hutchinson, et al.Bioorganic & Medicinal Chemistry Letters|October 31, 2007
Structure-activity relationships of adenosines with heterocyclic N6-substituentsT D Ashton, Kylee M Aumann, Stephen P Baker, et al.Organic Letters|March 14, 2003
Preparation of the 4-hydroxytryptamine scaffold via palladium-catalyzed cyclization: a practical and versatile synthesis of psilocinNicholas Gathergood, Peter J ScammellsThe Journal of Organic Chemistry|November 21, 2007
New methodology for the N-demethylation of opiate alkaloidsZemin Dong, Peter J ScammellsChemmedchem|June 28, 2016
Guidelines for the Synthesis of Small-Molecule Irreversible Probes Targeting G Protein-Coupled ReceptorsManuela Jörg, Peter J ScammellsPageof 20