#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA1174102	Binding	Inhibition of CDC2L5 at 10 uM		2	ALA1177794	single protein format	Scientific Literature
2.	ALA1837581	Binding	Inhibition of human CHED in HL60 cells lysate at 10 uM using post probe-labeling by LC-MS/MS analysis relative to control	Homo sapiens	5	ALA1833925	cell-based format	Scientific Literature
3.	ALA1908458	Binding	Binding constant for CDC2L5 kinase domain		72	ALA1908390	single protein format	Scientific Literature
4.	ALA4389146	Binding	Inhibition of wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in mammalian expression system at 10 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4387741	assay format	Scientific Literature
5.	ALA4389623	Binding	Inhibition of wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in mammalian expression system at 1 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4387741	assay format	Scientific Literature
6.	ALA4382427	Binding	Binding affinity to wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in mammalian expression system assessed as residual binding level at 1 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4382192	assay format	Scientific Literature
7.	ALA1944422	Binding	Inhibition of human CHED in HL-60 cells lysate assessed as reduction of labeling of acyl-phosphate ATP probe at 100 nM	Homo sapiens	4	ALA1938230	cell-based format	Scientific Literature
8.	ALA4365641	Binding	Inhibition of wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in mammalian expression system assessed as residual activity at 10 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4364269	assay format	Scientific Literature
9.	ALA2209339	Binding	Inhibition of CDC2L5 assessed as residual activity at 10 uM relative to control		1	ALA2203081	single protein format	Scientific Literature
10.	ALA3991653	Binding	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	242	ALA3991601	subcellular format	Kuster lab chemical proteomics drug profiling
11.	ALA4025049	Binding	Inhibition of wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in mammalian expression system assessed as residual activity at 1 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4024706	assay format	Scientific Literature
12.	ALA4043860	Binding	Inhibition of wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in HEK293 cells assessed as residual activity at 1000 nM after 30 mins by Kinomescan method relative to control	Homo sapiens	1	ALA4043093	cell-based format	Scientific Literature
13.	ALA4054987	Binding	Inhibition of wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in mammalian expression system assessed as residual activity at 50 nM by Kinomescan method relative to control	Homo sapiens	2	ALA4052645	assay format	Scientific Literature
14.	ALA4118325	Binding	Inhibition of CHED in human SKCO1 cells at 1 uM after 4 hrs using biotin labeled DIKCSNILLNNR probe by mass-spectrometric analysis relative to control	Homo sapiens	3	ALA4118021	cell-based format	Scientific Literature
15.	ALA4156939	Binding	Binding affinity to wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in mammalian expression system assessed as residual binding at 1 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4152344	assay format	Scientific Literature
16.	ALA4185718	Binding	Binding affinity to wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in HEK293 cells at 1 uM by Kinomescan method relative to control	Homo sapiens	2	ALA4184148	cell-based format	Scientific Literature
17.	ALA4230618	Binding	Binding affinity to wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in mammalian expression system assessed as residual binding level at 1 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4229344	assay format	Scientific Literature
18.	ALA4264207	Binding	Binding affinity to wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in mammalian expression system assessed as remaining unbound target protein level at 1000 nM by Kinomescan method relative to control	Homo sapiens	1	ALA4261600	assay format	Scientific Literature
19.	ALA4307723	Binding	Binding affinity to wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in mammalian expression system assessed as residual binding level at 10 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4304811	assay format	Scientific Literature
20.	ALA4333314	Binding	Binding affinity to wild-type human partial length CDC2L5 (H675 to S1054 residues) expressed in mammalian expression system assessed as residual binding level at 1 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4330132	assay format	Scientific Literature