| # | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
|---|---|---|---|---|---|---|---|---|---|
| 1. | ALA1837575 | B | Inhibition of human CDK10 in HL60 cells lysate at 10 uM using post probe-labeling by LC-MS/MS analysis relative to control | Homo sapiens | 5 | cell-based format | Scientific Literature | ||
| 2. | ALA2424245 | B | Inhibition of CDK10 in human PC3 cell lysates at 10 uM using desthiobiotin-tagged ATP probe AX9989 followed by trypsinization by LC/MS analysis | Homo sapiens | 12 | single protein format | Scientific Literature | ||
| 3. | ALA2424256 | B | Inhibition of CDK10 in human PC3 cell lysates at 30 uM using desthiobiotin-tagged ATP probe AX9989 followed by trypsinization by LC/MS analysis | Homo sapiens | 4 | single protein format | Scientific Literature | ||
| 4. | ALA3991651 | B | Kinobeads (epsilon), multiple immobilized ATP-competitive broad spectrum kinase inhibitors, used to assess residual binding of ~300 proteins simultaneously from cell lysate in the presence of a compound. Quantitative readout performed by mass spectrometry. | Homo sapiens | 65 | subcellular format | Kuster lab chemical proteomics drug profiling | ||
| 5. | ALA4034286 | B | Inhibition of CDK10 Lysine 2 labelling site (unknown origin) at 10 uM | Homo sapiens | 1 | single protein format | Scientific Literature | ||
| 6. | ALA4375313 | B | Binding affinity to wild-type human full-length CDK10 (M1 to P360 residues) expressed in mammalian expression system measured after 1 hr by kinomescan method | Homo sapiens | 1 | assay format | Scientific Literature |
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