# | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. | ALA896510 | F | Inhibition of Eg5 assessed as inhibition ATP hydrolysis by ATPase assay | 21 | assay format | Scientific Literature | |||
2. | ALA896511 | F | Cytotoxic activity against HeLa cells | Homo sapiens | 21 | cell-based format | Scientific Literature | ||
3. | ALA1250155 | B | Binding affinity to Bacillus subtilis 168 1A1 lysine riboswitch 179 lysc by in-line probing assay | Bacillus subtilis subsp. subtilis str. 168 | 14 | nucleic acid format | Scientific Literature | ||
4. | ALA1614027 | A | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9. (Class of assay: confirmatory) [Related pubchem assays: 885, 884, 410 ] | Homo sapiens | 2,933 | single protein format | PubChem BioAssays | ||
5. | ALA1741321 | F | PUBCHEM_BIOASSAY: Cytochrome panel assay with activity outcomes. (Class of assay: other) Panel member name: p450-cyp2d6 Compounds with AC50 equal or less than 10 uM are considered active | 16,572 | assay format | PubChem BioAssays | |||
6. | ALA1741322 | F | PUBCHEM_BIOASSAY: Cytochrome panel assay with activity outcomes. (Class of assay: other) Panel member name: p450-cyp1a2 Compounds with AC50 equal or less than 10 uM are considered active | 16,572 | assay format | PubChem BioAssays | |||
7. | ALA1741323 | F | PUBCHEM_BIOASSAY: Cytochrome panel assay with activity outcomes. (Class of assay: other) Panel member name: p450-cyp2c19 Compounds with AC50 equal or less than 10 uM are considered active | 16,572 | assay format | PubChem BioAssays | |||
8. | ALA1741324 | F | PUBCHEM_BIOASSAY: Cytochrome panel assay with activity outcomes. (Class of assay: other) Panel member name: p450-cyp3a4 Compounds with AC50 equal or less than 10 uM are considered active | 16,572 | assay format | PubChem BioAssays | |||
9. | ALA1741325 | F | PUBCHEM_BIOASSAY: Cytochrome panel assay with activity outcomes. (Class of assay: other) Panel member name: p450-cyp2c9 Compounds with AC50 equal or less than 10 uM are considered active | 16,572 | assay format | PubChem BioAssays | |||
10. | ALA3282985 | P | Dissociation constant, pKa of the compound | 4 | small-molecule physicochemical format | Scientific Literature | |||
11. | ALA3282986 | B | Activity of Escherichia coli B lysyl-tRNA ligase after 15 mins by Lineweaver-Burk plot analysis | Escherichia coli B | 3 | assay format | Scientific Literature | ||
12. | ALA3282998 | F | Cytotoxicity against mouse P388 cells assessed as growth inhibition at 0.5 mM after 72 hrs by hemocytometry | Mus musculus | 1 | cell-based format | Scientific Literature | ||
13. | ALA3428767 | B | Binding affinity to lysC riboswitch in Bacillus subtilis | Bacillus subtilis | 5 | assay format | Scientific Literature | ||
14. | ALA3428776 | F | Antibacterial activity against Bacillus subtilis in chemical defined medium | Bacillus subtilis | 2 | organism-based format | Scientific Literature | ||
15. | ALA4334751 | B | Inhibition of Escherichia coli dihydrodipicolinate synthase at 4.6 mM relative to control | Escherichia coli | 1 | single protein format | Scientific Literature | ||
16. | ALA4334752 | B | Competitive inhibition of Escherichia coli dihydrodipicolinate synthase using DL-ASA as substrate | Escherichia coli | 3 | single protein format | Scientific Literature | ||
17. | ALA4334754 | B | Uncompetitive inhibition of Escherichia coli dihydrodipicolinate synthase using DL-ASA as substrate | Escherichia coli | 4 | single protein format | Scientific Literature | ||
18. | ALA4334764 | B | Uncompetitive inhibition of Escherichia coli dihydrodipicolinate synthase using pyruvate as substrate | Escherichia coli | 1 | single protein format | Scientific Literature |