#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA1168790	B	Inhibition of ASK2 at 1 uM		8	ALA1165965	single protein format	Scientific Literature
2.	ALA1174072	B	Inhibition of ASK2 at 10 uM		2	ALA1177794	single protein format	Scientific Literature
3.	ALA1244728	B	Binding affinity to ASK2		7	ALA1240346	single protein format	Scientific Literature
4.	ALA1827645	B	Activity of ASK2 kinase at 1 uM		1	ALA1821651	single protein format	Scientific Literature
5.	ALA1908659	B	Binding constant for ASK2 kinase domain		72	ALA1908390	single protein format	Scientific Literature
6.	ALA2212073	B	Inhibition of ASK2 assessed as residual activity at 10 uM relative to control		1	ALA2203081	single protein format	Scientific Literature
7.	ALA2214714	B	Inhibition of ASK2		1	ALA2203246	single protein format	Scientific Literature
8.	ALA3631908	B	Inhibition of MEKK6 (unknown origin) at 10 uM after 120 mins P33 radiolabeled kinase activity assay	Homo sapiens	3	ALA3627608	single protein format	Scientific Literature
9.	ALA3991763	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	238	ALA3991601	subcellular format	Kuster lab chemical proteomics drug profiling
10.	ALA4012569	B	Binding affinity to MAP3K6 in human INA-6 cells after 3 hrs by nanoLC-MS/MS method	Homo sapiens	2	ALA4011617	cell-based format	Scientific Literature
11.	ALA4025017	B	Inhibition of wild-type human partial length ASK2 (M278 to R972 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.	ALA4034388	B	Inhibition of MAP3K6 Lysine 2 labelling site (unknown origin) at 10 uM	Homo sapiens	1	ALA4033637	single protein format	Scientific Literature
13.	ALA4043828	B	Inhibition of wild-type human partial length ASK2 (M278 to R972 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
14.	ALA4045742	B	Inhibition of MAP3K6 conserved Lys1 (IAIKEIPER) in human PBMC at 1 uM	Homo sapiens	1	ALA4043168	single protein format	Scientific Literature
15.	ALA4045748	B	Inhibition of MAP3K6 conserved Lys2 (DIKGDNVLINTFSGLLK) in human PBMC at 1 uM	Homo sapiens	1	ALA4043168	single protein format	Scientific Literature
16.	ALA4045983	B	Inhibition of MAP3K6 conserved Lys1 (IAIKEIPER) in human PBMC at 0.1 uM	Homo sapiens	1	ALA4043168	single protein format	Scientific Literature
17.	ALA4045989	B	Inhibition of MAP3K6 conserved Lys2 (DIKGDNVLINTFSGLLK) in human PBMC at 0.1 uM	Homo sapiens	1	ALA4043168	single protein format	Scientific Literature
18.	ALA4054946	B	Inhibition of wild-type human partial length MAP3K6 (M278 to R972 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
19.	ALA4156907	B	Binding affinity to wild-type human partial length ASK2 (M278 to R972 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
20.	ALA4185686	B	Binding affinity to wild-type human partial length ASK2 (M278 to R972 residues) expressed in HEK293 cells at 1 uM by Kinomescan method relative to control	Homo sapiens	2	ALA4184148	cell-based format	Scientific Literature