| # | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
|---|---|---|---|---|---|---|---|---|---|
| 1. | ALA3738004 | F | Antagonist activity at human beta2 receptor expressed in CHO-K1 cells assessed as isoproterenol-induced cAMP level by HTRF assay | Homo sapiens | 3 | ALA3734721 | cell-based format | Scientific Literature | |
| 2. | ALA3738005 | F | Antagonist activity at human beta1 receptor expressed in CHO-K1 cells assessed as isoproterenol-induced cAMP level by HTRF assay | Homo sapiens | 3 | ALA3734721 | cell-based format | Scientific Literature | |
| 3. | ALA3738006 | P | Chemical stability of compound in DMSO assessed as compound remaining at 10 mg/ml after 2 days at room temperature | 3 | ALA3734721 | small-molecule physicochemical format | Scientific Literature | ||
| 4. | ALA3738007 | P | Chemical stability of compound in DMSO assessed as compound remaining at 10 mg/ml after 24 days at room temperature under air | 3 | ALA3734721 | small-molecule physicochemical format | Scientific Literature | ||
| 5. | ALA3738008 | P | Chemical stability of compound in 0.1N HCL assessed as compound remaining at 10 mg/ml after 1 day | 3 | ALA3734721 | small-molecule physicochemical format | Scientific Literature | ||
| 6. | ALA3738009 | P | Chemical stability of compound in 0.1N HCL and 0.5% H2O2 assessed as compound remaining at 10 mg/ml after 1 day | 3 | ALA3734721 | small-molecule physicochemical format | Scientific Literature | ||
| 7. | ALA3738010 | P | Chemical stability of compound in 0.1N NaOH assessed as compound remaining at 10 mg/ml after 1 day | 3 | ALA3734721 | small-molecule physicochemical format | Scientific Literature | ||
| 8. | ALA3738113 | P | Chemical stability of compound in 0.1N NaOH assessed as compound remaining at 10 mg/ml after 2 days | 3 | ALA3734721 | small-molecule physicochemical format | Scientific Literature | ||
| 9. | ALA3738114 | P | Chemical stability of compound in buffer at pH 7.4 assessed as compound remaining at 10 mg/ml after 1 day | 3 | ALA3734721 | small-molecule physicochemical format | Scientific Literature | ||
| 10. | ALA3738115 | P | Chemical stability of compound in buffer at pH 7.4 assessed as compound remaining at 10 mg/ml after 2 days | 3 | ALA3734721 | small-molecule physicochemical format | Scientific Literature | ||
| 11. | ALA3738116 | P | Chemical stability of compound in DMSO assessed as compound remaining at 10 mg/ml after 1 day at room temperature | 3 | ALA3734721 | small-molecule physicochemical format | Scientific Literature | ||
| 12. | ALA3738117 | F | Antagonist activity at human 5-HT1A receptor expressed in CHO-K1 cells assessed as seretonin-induced cAMP level by HTRF assay | Homo sapiens | 3 | ALA3734721 | cell-based format | Scientific Literature | |
| 13. | ALA3738118 | F | Antagonist activity at human 5-HT1B receptor expressed in CHO-K1 cells assessed as seretonin-induced cAMP level by HTRF assay | Homo sapiens | 3 | ALA3734721 | cell-based format | Scientific Literature | |
| 14. | ALA3738119 | F | Antagonist activity at human 5-HT2A receptor expressed in CHO-K1 cells assessed as seretonin-induced calcium level by FDSS assay | Homo sapiens | 3 | ALA3734721 | cell-based format | Scientific Literature | |
| 15. | ALA3738120 | F | Antagonist activity at human 5-HT2B receptor expressed in CHO-K1 cells assessed as seretonin-induced calcium level by FDSS assay | Homo sapiens | 3 | ALA3734721 | cell-based format | Scientific Literature | |
| 16. | ALA3738121 | F | Antagonist activity at human 5-HT2C receptor expressed in CHO-K1 cells assessed as seretonin-induced calcium level by FDSS assay | Homo sapiens | 3 | ALA3734721 | cell-based format | Scientific Literature | |
| 17. | ALA3738122 | F | Antagonist activity at human 5-HT6 receptor expressed in 1321N1 cells assessed as seretonin-induced cAMP by HTRF assay | Homo sapiens | 3 | ALA3734721 | cell-based format | Scientific Literature | |
| 18. | ALA3738123 | F | Antagonist activity at human wild-type 5-HT7 receptor expressed in HEK cells assessed as seretonin-induced cAMP by HTRF assay | Homo sapiens | 3 | ALA3734721 | cell-based format | Scientific Literature | |
| 19. | ALA3738124 | F | Antagonist activity at human wild-type A2A receptor expressed in CHO-K1 cells assessed as NECA-induced cAMP by HTRF assay | Homo sapiens | 3 | ALA3734721 | cell-based format | Scientific Literature | |
| 20. | ALA3738125 | F | Antagonist activity at human wild-type A3 receptor expressed in CHO-K1 cells assessed as IB MECA-induced cAMP by HTRF assay | Homo sapiens | 3 | ALA3734721 | cell-based format | Scientific Literature |
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