ud cg 212 cl has been researched along with 1,3-dipropyl-8-cyclopentylxanthine in 1 studies
| Studies (ud cg 212 cl) | Trials (ud cg 212 cl) | Recent Studies (post-2010) (ud cg 212 cl) | Studies (1,3-dipropyl-8-cyclopentylxanthine) | Trials (1,3-dipropyl-8-cyclopentylxanthine) | Recent Studies (post-2010) (1,3-dipropyl-8-cyclopentylxanthine) |
|---|---|---|---|---|---|
| 28 | 2 | 0 | 1,301 | 1 | 165 |
| Protein | Taxonomy | ud cg 212 cl (IC50) | 1,3-dipropyl-8-cyclopentylxanthine (IC50) |
|---|---|---|---|
| Adenosine receptor A1 | Rattus norvegicus (Norway rat) | 0.0051 | |
| Adenosine receptor A3 | Rattus norvegicus (Norway rat) | 0.0038 | |
| Adenosine receptor A2a | Homo sapiens (human) | 0.2033 | |
| Adenosine receptor A2b | Homo sapiens (human) | 0.0234 | |
| Adenosine receptor A1 | Homo sapiens (human) | 0.0083 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (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 |
|---|---|
| Böhm, M; Erdmann, E; Schwinger, RH; Ungerer, M | 1 |
1 other study(ies) available for ud cg 212 cl and 1,3-dipropyl-8-cyclopentylxanthine
| Article | Year |
|---|---|
Antagonism of novel inotropic agents at A1 adenosine receptors and m-cholinoceptors in human myocardium.
Topics: Adult; Binding, Competitive; Cardiotonic Agents; Electric Stimulation; Guanylyl Imidodiphosphate; Heart; Heart Failure; Humans; Imidazoles; In Vitro Techniques; Membranes; Milrinone; Myocardium; Piperazines; Pyridazines; Pyridones; Quinuclidinyl Benzilate; Receptors, Cholinergic; Receptors, Purinergic; Xanthines | 1990 |