sch 58261 has been researched along with n-(1-methyl-2-phenylethyl)adenosine, (s)-isomer in 2 studies
| Studies (sch 58261) | Trials (sch 58261) | Recent Studies (post-2010) (sch 58261) | Studies (n-(1-methyl-2-phenylethyl)adenosine, (s)-isomer) | Trials (n-(1-methyl-2-phenylethyl)adenosine, (s)-isomer) | Recent Studies (post-2010) (n-(1-methyl-2-phenylethyl)adenosine, (s)-isomer) |
|---|---|---|---|---|---|
| 46 | 0 | 14 | 20 | 0 | 2 |
| Protein | Taxonomy | sch 58261 (IC50) | n-(1-methyl-2-phenylethyl)adenosine, (s)-isomer (IC50) |
|---|---|---|---|
| Adenosine receptor A1 | Rattus norvegicus (Norway rat) | 0.105 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Schofield, PR; Townsend-Nicholson, A | 1 |
| Arslan, G; Dionisotti, S; Fredholm, BB; Kull, B; Ongini, E; Zocchi, C | 1 |
2 other study(ies) available for sch 58261 and n-(1-methyl-2-phenylethyl)adenosine, (s)-isomer
| Article | Year |
|---|---|
A threonine residue in the seventh transmembrane domain of the human A1 adenosine receptor mediates specific agonist binding.
Topics: Adenosine; Adenosine-5'-(N-ethylcarboxamide); Amino Acid Sequence; Binding Sites; Binding, Competitive; Brain; Cell Membrane; Humans; Kinetics; Mutagenesis, Site-Directed; Point Mutation; Radioligand Assay; Receptors, Purinergic P1; Recombinant Proteins; Stereoisomerism; Theophylline; Threonine; Tritium | 1994 |
Characterization of human A2A adenosine receptors with the antagonist radioligand [3H]-SCH 58261.
Topics: Animals; Binding, Competitive; CHO Cells; Cricetinae; Cyclic AMP; Humans; Purinergic P1 Receptor Antagonists; Pyrimidines; Radioligand Assay; Rats; Receptor, Adenosine A2A; Receptors, Purinergic P1; Species Specificity; Transfection; Triazoles | 1997 |