cgs 15943 and vuf 8504
cgs 15943 has been researched along with vuf 8504 in 3 studies
Research
Studies (3)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
Authors
| Authors | Studies |
|---|---|
| de Groote, M; Frijtag von Drabbe Künzel, J; IJzerman, AP; Timmerman, H; van Muijlwijk-Koezen, JE; Visser, S; Vollinga, RC | 1 |
| Barak, D; Chen, A; Gao, ZG; Jacobson, KA; Kim, SA; Lee, K; Liang, BT; Link, A; Rompaey, PV; van Calenbergh, S | 1 |
| Andreini, M; Baraldi, PG; Bernardini, C; Borea, PA; Botta, M; Corelli, F; Fruttarolo, F; Martinelli, A; Ortore, G; Tafi, A; Tuccinardi, T | 1 |
Other Studies
3 other study(ies) available for cgs 15943 and vuf 8504
| Article | Year |
|---|---|
Thiazole and thiadiazole analogues as a novel class of adenosine receptor antagonists.
Topics: Animals; Brain; Cyclohexylamines; In Vitro Techniques; Models, Molecular; Molecular Conformation; Purinergic P1 Receptor Antagonists; Radioligand Assay; Rats; Receptor, Adenosine A2A; Receptor, Adenosine A3; Receptors, Purinergic P1; Structure-Activity Relationship; Thiadiazoles; Thiazoles | 2001 |
Neoceptor concept based on molecular complementarity in GPCRs: a mutant adenosine A(3) receptor with selectively enhanced affinity for amine-modified nucleosides.
Topics: Adenosine; Amines; Animals; Cell Line; Cerebral Cortex; Cyclic AMP; GTP-Binding Proteins; Humans; In Vitro Techniques; Ligands; Models, Molecular; Purinergic P1 Receptor Agonists; Purinergic P1 Receptor Antagonists; Radioligand Assay; Rats; Receptor, Adenosine A3; Receptors, Purinergic P1 | 2001 |
Pharmacophore based receptor modeling: the case of adenosine A3 receptor antagonists. An approach to the optimization of protein models.
Topics: Adenosine A3 Receptor Antagonists; Animals; Binding, Competitive; CHO Cells; Cricetinae; Cricetulus; Drug Design; Furans; Humans; Models, Molecular; Molecular Structure; Pyrazoles; Pyrimidines; Radioligand Assay; Receptor, Adenosine A3; Thermodynamics; Triazoles | 2006 |