# | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. | ALA638274 | P | Solubility in water at PH 7.4 in the presence of Tris.HCl buffer | 12 | ALA1124058 | small-molecule physicochemical format | Scientific Literature | ||
2. | ALA648306 | B | Antagonistic activity on N6-([3H]-phenylisopropyl)adenosine binding to rat brain membrane (Adenosine A1 receptor) | 20 | ALA1124058 | tissue-based format | Scientific Literature | ||
3. | ALA697366 | B | Inhibition of 5'-(N-ethylcarbamoyl)adenosine-elicited stimulation of adenylate cyclase in human platelet membranes | 22 | ALA1124058 | cell membrane format | Scientific Literature | ||
4. | ALA757574 | F | Inhibition of 5'-(N-ethylcarbamoyl)adenosine-elicited stimulation of adenylate cyclase in rat PC12 cell membranes | 12 | ALA1124058 | cell membrane format | Scientific Literature | ||
5. | ALA845121 | F | Ratio of antagonist activity at A1 and A2 receptors | Rattus norvegicus | 22 | ALA1124058 | assay format | Scientific Literature | |
6. | ALA5223693 | B | Binding affinity to human A1 adenosine receptor assessed as inhibition constant | Homo sapiens | 3 | ALA5223081 | single protein format | Scientific Literature | |
7. | ALA5223710 | B | Selectivity index, ratio of Ki for human A2 receptor to Ki for A1 receptor assessed as fold change | Homo sapiens | 4 | ALA5223081 | assay format | Scientific Literature |