# | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. | ALA631694 | P | Partition coefficient (logP) | 50 | small-molecule physicochemical format | Scientific Literature | |||
2. | ALA631695 | P | Partition coefficient (logP) (benzene) | 50 | small-molecule physicochemical format | Scientific Literature | |||
3. | ALA875968 | P | Partition coefficient (logP) (carbon tetrachloride) | 50 | small-molecule physicochemical format | Scientific Literature | |||
4. | ALA632430 | P | Partition coefficient (logP) (chloroform) | 50 | small-molecule physicochemical format | Scientific Literature | |||
5. | ALA632431 | P | Partition coefficient (logP) (ether) | 50 | small-molecule physicochemical format | Scientific Literature | |||
6. | ALA632432 | P | Partition coefficient (logP) (hexane) | 50 | small-molecule physicochemical format | Scientific Literature | |||
7. | ALA856985 | F | Compound was evaluated for inhibitory activity against Candida albicans; 3.2-4 | Candida albicans | 1 | organism-based format | Scientific Literature | ||
8. | ALA704804 | F | Compound was evaluated for erythroid induction of benzidine-positive K562 cells at concentration 4 mM after 9 day induction period | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
9. | ALA705727 | F | Inhibition of cell growth against human myeloid leukemia K562(S) cells | Homo sapiens | 17 | cell-based format | Scientific Literature | ||
10. | ALA803027 | F | Compound was evaluated for inhibitory activity against Saccharomyces cerevisiae; 3.2-4 | Saccharomyces cerevisiae | 1 | organism-based format | Scientific Literature | ||
11. | ALA876466 | P | Lipophilicity determined as logarithm of the partition coefficient in the alkane/water system | 181 | small-molecule physicochemical format | Scientific Literature | |||
12. | ALA991844 | P | Dissociation constant, pKa of the compound | 51 | small-molecule physicochemical format | Scientific Literature | |||
13. | ALA1008236 | B | Inhibition of mouse Oat6-mediated [3H]ES uptake in Xenopus oocytes after 1 hr | Mus musculus | 45 | cell-based format | Scientific Literature | ||
14. | ALA1008237 | B | Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hr | Mus musculus | 45 | cell-based format | Scientific Literature | ||
15. | ALA1008238 | B | Ratio of pKi for mouse Oat1 expressed in Xenopus oocytes to pKi for mouse Oat6 expressed in Xenopus oocytes | Mus musculus | 45 | cell-based format | Scientific Literature | ||
16. | ALA1040171 | B | Inhibition of HDAC in human Hela cells nuclear extracts assessed as residual activity at 500 uM by fluorimetric assay | Homo sapiens | 33 | cell-based format | Scientific Literature | ||
17. | ALA1069216 | F | Agonist activity at human FFA2 receptor expressed in CHO cells assessed as inhibition of forskolin-induced cAMP production | Homo sapiens | 85 | cell-based format | Scientific Literature | ||
18. | ALA1069226 | F | Agonist activity at human FFA2 receptor expressed in CHO cells assessed as inhibition of forskolin-induced cAMP production relative to acetate | Homo sapiens | 85 | cell-based format | Scientific Literature | ||
19. | ALA1220788 | T | Toxicity in po dosed mouse | Mus musculus | 7 | organism-based format | Scientific Literature | ||
20. | ALA1921590 | B | Inhibition of calf DNA polymerase alpha using poly(dA)/oligo(dT)18 (A/T = 2/1) and dTTP as the DNA template-primer and nucleotide substrate at 10 uM after 60 mins | Bos taurus | 21 | assay format | Scientific Literature |