# | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. | ALA645178 | B | Dissociation constant from Alcohol dehydrogenase | Equus caballus | 1 | protein format | Scientific Literature | ||
2. | ALA645180 | B | In vitro inhibitory activity against horse liver Alcohol dehydrogenase (ADH) | Equus caballus | 1 | assay format | Scientific Literature | ||
3. | ALA683666 | B | In vitro inhibitory activity against bovine liver glutamate dehydrogenase (GDH) | 4 | assay format | Scientific Literature | |||
4. | ALA698172 | B | Inhibition of inosine monophosphate dehydrogenase (IMPDH) enzyme by Non-competitive inhibition | 1 | assay format | Scientific Literature | |||
5. | ALA698173 | B | Inhibition of partially purified preparation of Inosine-5'-monophosphate dehydrogenase from P388 leukemic cells with chemically synthesized dinucleotide | 1 | cell-based format | Scientific Literature | |||
6. | ALA698174 | B | Inhibition of partially purified preparation of Inosine-5'-monophosphate dehydrogenase from P388 leukemic cells with enzymatically synthesized dinucleotide | 1 | cell-based format | Scientific Literature | |||
7. | ALA698179 | B | Noncompetitive inhibitory activity against Inosine-5'-monophosphate dehydrogenase using NAD as viable substrate | 4 | assay format | Scientific Literature | |||
8. | ALA698509 | B | Uncompetitive Inhibitory activity against Inosine-5'-monophosphate dehydrogenase using IMP as viable substrate | 4 | assay format | Scientific Literature | |||
9. | ALA698512 | B | Compound was tested for inhibitory activity against Inosine-5'-monophosphate dehydrogenase, the type of inhibition in not competitive | 4 | single protein format | Scientific Literature | |||
10. | ALA698517 | B | The compound was tested for the inhibition towards IMP(Inosine 5'-monophosphate) substrate of Inosine-5'-monophosphate dehydrogenase 1 | 5 | single protein format | Scientific Literature | |||
11. | ALA698518 | B | The compound was tested for the inhibition towards NMD (Nicotinamide adenine dinucleotide) substrate of Inosine-5'-monophosphate dehydrogenase 1 | 5 | single protein format | Scientific Literature | |||
12. | ALA699560 | B | The compound was assayed to determine the inhibitory activity against human Inosine-5'-monophosphate dehydrogenase 2 | 9 | single protein format | Scientific Literature | |||
13. | ALA699567 | B | The compound was tested for the inhibition towards IMP(Inosine 5'-monophosphate) substrate of Inosine-5'-monophosphate dehydrogenase 2 | 5 | single protein format | Scientific Literature | |||
14. | ALA699568 | B | The compound was tested for the inhibition towards NMD (Nicotinamide adenine dinucleotide) substrate of Inosine-5'-monophosphate dehydrogenase 2 | 5 | single protein format | Scientific Literature | |||
15. | ALA699569 | B | Inhibitory binding constant was determined against human Inosine-5'-monophosphate dehydrogenase 2 (IMPDH type II) from intercept of Michaelis-Menten plot | 7 | single protein format | Scientific Literature | |||
16. | ALA699570 | B | Inhibitory binding constant was determined against human Inosine-5'-monophosphate dehydrogenase 2 (IMPDH type II) from slope of Michaelis-Menten plot | 7 | single protein format | Scientific Literature | |||
17. | ALA700387 | F | The concentration used to induce differentiation in K562 cells | Homo sapiens | 10 | cell-based format | Scientific Literature | ||
18. | ALA700521 | F | Antiproliferative activity against K562 erythroid leukemic cells was determined. | Homo sapiens | 9 | cell-based format | Scientific Literature | ||
19. | ALA700220 | F | The ability to induce differentiation in K562 cells was estimated by determining the fraction of benzidine positive cells converted following incubation with the compound. | Homo sapiens | 10 | cell-based format | Scientific Literature | ||
20. | ALA701427 | F | Compound effect on differentiation of K562 cells, % of benzidine positive cells at 1.0 uM | Homo sapiens | 9 | cell-based format | Scientific Literature |