# | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. | ALA4122259 | A | Half life in mouse liver microsomes at 3 uM preincubated for 5 mins followed by NADPH addition by LC-MS/MS analysis | Mus musculus | 3 | ALA4118144 | microsome format | Scientific Literature | |
2. | ALA4122260 | A | Half life in human liver microsomes at 3 uM preincubated for 5 mins followed by NADPH addition by LC-MS/MS analysis | Homo sapiens | 3 | ALA4118144 | microsome format | Scientific Literature | |
3. | ALA4122261 | P | Kinetic solubility of the compound in PBS at pH 7.4 at 6.75 to 200 uM after 90 mins by UV absorbance based assay | 3 | ALA4118144 | small-molecule physicochemical format | Scientific Literature | ||
4. | ALA4122262 | B | Inhibition of recombinant C-terminal His10-tagged human Hepsin (R45 to L17 residues) D161E/ R162K double mutant expressed in mouse NS0 cells using Boc-QRR-AMC as substrate after 15 mins by automated fluorescence assay | Homo sapiens | 35 | ALA4118144 | cell-based format | Scientific Literature | |
5. | ALA4122263 | B | Inhibition of recombinant C-terminal His10-tagged human uPA (M1 to L431 residues) expressed in mouse NS0 cells using Z-GGR-AMC as substrate after 15 mins by automated fluorescence assay | Homo sapiens | 34 | ALA4118144 | cell-based format | Scientific Literature | |
6. | ALA4122264 | B | Selectivity ratio of IC50 for recombinant C-terminal His10-tagged human uPA (M1 to L431 residues) to IC50 for recombinant C-terminal His10-tagged human Hepsin (R45 to L17 residues) D161E/ R162K double mutant by automated fluorescence assay | Homo sapiens | 21 | ALA4118144 | assay format | Scientific Literature | |
7. | ALA4122265 | B | Inhibition of recombinant C-terminal His10-tagged human Hepsin (R45 to L17 residues) D161E/ R162K double mutant expressed in mouse NS0 cells using Boc-QRR-AMC as substrate after 15 mins by manual fluorescence assay | Homo sapiens | 8 | ALA4118144 | cell-based format | Scientific Literature | |
8. | ALA4122266 | B | Inhibition of recombinant C-terminal His10-tagged human uPA (M1 to L431 residues) expressed in mouse NS0 cells using Z-GGR-AMC as substrate after 15 mins by manual fluorescence assay | Homo sapiens | 7 | ALA4118144 | cell-based format | Scientific Literature | |
9. | ALA4122267 | B | Selectivity ratio of IC50 for recombinant C-terminal His10-tagged human uPA (M1 to L431 residues) to IC50 for recombinant C-terminal His10-tagged human Hepsin (R45 to L17 residues) D161E/ R162K double mutant by manual fluorescence assay | Homo sapiens | 7 | ALA4118144 | assay format | Scientific Literature | |
10. | ALA4122268 | A | Apparent permeability of the compound at 50 to 200 uM after 5 hrs by PAMPA | 3 | ALA4118144 | assay format | Scientific Literature | ||
11. | ALA4122269 | A | Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 48 hrs by CellTiter-Blue/CytoTox-ONE-based assay | Homo sapiens | 3 | ALA4118144 | cell-based format | Scientific Literature | |
12. | ALA4122270 | B | Inhibition of doxycycline induced Hepsin in human MCF10A cells using Boc-QRR-AMC as substrate preincubated for 24 hrs followed by doxycycline induction for 24 hrs and subsequent addition of substrate by fluorescence assay | Homo sapiens | 5 | ALA4118144 | cell-based format | Scientific Literature | |
13. | ALA4122271 | B | Inhibition of doxycycline induced Hepsin in human MCF10A cells assessed as prevention in loss of HAI-1 level at 10 uM preincubated for 30 mins followed by doxycycline addition measured after 6 hrs by Immunoblot assay | Homo sapiens | 5 | ALA4118144 | cell-based format | Scientific Literature | |
14. | ALA4122274 | B | Inhibition of hepsin-mediated conversion of Pro-HGF into active form in human Hs578T cells assessed as decrease in MET phosphorylation at 1 to 10 uM preincubated for 30 mins followed by recombinant human pro-HGF addition measured after 30 mins by immunoblot method | Homo sapiens | 5 | ALA4118144 | cell-based format | Scientific Literature | |
15. | ALA4122282 | B | Inhibition of human thrombin using Z-Gly-Pro-Arg-AMC as substrate at 1 uM after 60 mins by fluorescence spectrophotometric method relative to control | Homo sapiens | 3 | ALA4118144 | single protein format | Scientific Literature | |
16. | ALA4122283 | B | Inhibition of human thrombin using Z-Gly-Pro-Arg-AMC as substrate at 10 uM after 60 mins by fluorescence spectrophotometric method relative to control | Homo sapiens | 3 | ALA4118144 | single protein format | Scientific Literature | |
17. | ALA4122284 | B | Inhibition of human chymase using Suc-Ala-Ala-Pro-Phe-AMC as substrate at 1 uM after 120 mins by fluorescence spectrophotometric method relative to control | Homo sapiens | 3 | ALA4118144 | single protein format | Scientific Literature | |
18. | ALA4122285 | B | Inhibition of human chymase using Suc-Ala-Ala-Pro-Phe-AMC as substrate at 10 uM after 120 mins by fluorescence spectrophotometric method relative to control | Homo sapiens | 3 | ALA4118144 | single protein format | Scientific Literature | |
19. | ALA4122286 | B | Inhibition of elastase (unknown origin) at 1 uM relative to control | Homo sapiens | 3 | ALA4118144 | single protein format | Scientific Literature | |
20. | ALA4122287 | B | Inhibition of elastase (unknown origin) at 10 uM relative to control | Homo sapiens | 3 | ALA4118144 | single protein format | Scientific Literature |