| # | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
|---|---|---|---|---|---|---|---|---|---|
| 1. | ALA636408 | A | Half life period was determined | 7 | ALA1124997 | assay format | Scientific Literature | ||
| 2. | ALA634032 | A | kinact was determined. | 8 | ALA1125454 | assay format | Scientific Literature | ||
| 3. | ALA876340 | A | Half-life period of the compound | 8 | ALA1125454 | assay format | Scientific Literature | ||
| 4. | ALA645585 | B | Inhibition of cytochrome P450 19A1 aromatase from human placental microsomes | Homo sapiens | 7 | ALA1151017 | assay format | Scientific Literature | |
| 5. | ALA666775 | B | Inhibition of mouse constitutive androstane receptor (mCAR) activity at 10 uM was determined as percent remaining activity | Mus musculus | 46 | ALA1145136 | single protein format | Scientific Literature | |
| 6. | ALA666801 | B | Inhibition of 1 uM [1-beta-3H]-androstenedione binding to human placental microsome Cytochrome P450 19A1 | Homo sapiens | 14 | ALA1125884 | assay format | Scientific Literature | |
| 7. | ALA664248 | B | Inhibition of cytochrome P450 19A1 | Homo sapiens | 10 | ALA1125454 | single protein format | Scientific Literature | |
| 8. | ALA657130 | B | Inhibition of Cytochrome P450 19A1 at the concentration of 0.25 uM | 17 | ALA1123161 | single protein format | Scientific Literature | ||
| 9. | ALA657131 | B | Inhibition of Cytochrome P450 19A1 at the concentration of 0.75 uM | 17 | ALA1123161 | single protein format | Scientific Literature | ||
| 10. | ALA657132 | B | Inhibition of Cytochrome P450 19A1 at the concentration of 1.5 uM | 17 | ALA1123161 | single protein format | Scientific Literature | ||
| 11. | ALA657133 | B | Inhibition of 0.25 uM [1-3H]-androst-4-ene-3,17-dione binding to Cytochrome P450 19A1 | Homo sapiens | 8 | ALA1122664 | single protein format | Scientific Literature | |
| 12. | ALA657134 | B | Inhibition of 1.25 uM [1-3H]-androst-4-ene-3,17-dione binding to Cytochrome P450 19A1 | Homo sapiens | 8 | ALA1122664 | single protein format | Scientific Literature | |
| 13. | ALA657135 | B | Percent inhibition of human placental Cytochrome P450 19A1 at 1:1 inhibitor: androstenedione (0.7 uM) ratio | 5 | ALA1123074 | assay format | Scientific Literature | ||
| 14. | ALA661748 | B | Percent inhibition of human placental Cytochrome P450 19A1 at 3:1 inhibitor: androstenedione (0.7 uM) ratio | 5 | ALA1123074 | assay format | Scientific Literature | ||
| 15. | ALA661762 | B | Binding affinity was measured on Cytochrome P450 19A1 | 29 | ALA1124997 | single protein format | Scientific Literature | ||
| 16. | ALA664581 | B | Inhibition constant for human placental cytochrome P450 19A1 | Homo sapiens | 4 | ALA1125454 | assay format | Scientific Literature | |
| 17. | ALA666399 | B | Evaluated for its competitive inhibitory activity against Cytochrome P450 19A1 with the use of human placental microsomal preparation | 7 | ALA1123161 | assay format | Scientific Literature | ||
| 18. | ALA664416 | B | Percent inhibition of human placental Cytochrome P450 19A1 at 1:1 inhibitor: androstenedione (0.7 uM) ratio | Rattus norvegicus | 5 | ALA1123074 | assay format | Scientific Literature | |
| 19. | ALA664417 | B | Percent inhibition of human placental Cytochrome P450 19A1 at 3:1 inhibitor: androstenedione (0.7 uM) ratio | Rattus norvegicus | 18 | ALA1123074 | assay format | Scientific Literature | |
| 20. | ALA765531 | B | Maximum absorbance for formation of reversible-enzyme-ligand complexes with human placental aromatase (PL1) | Homo sapiens | 8 | ALA1124325 | assay format | Scientific Literature |
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