#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA1826627	B	Activity of EPHB6 kinase at 1 uM		1		single protein format	Scientific Literature
2.	ALA1908654	B	Binding constant for EPHB6 kinase domain		72		single protein format	Scientific Literature
3.	ALA1049969	B	Binding affinity to EPHB6 assessed as percentage of kinase remaining bound to the bead at 1 uM by T7 phage display based binding assay		1		single protein format	Scientific Literature
4.	ALA1169217	B	Inhibition of EPHB6 at 1 uM		6		single protein format	Scientific Literature
5.	ALA1174407	B	Inhibition of EPHB6 at 10 uM		2		single protein format	Scientific Literature
6.	ALA1244824	B	Binding affinity to EPHB6		7		single protein format	Scientific Literature
7.	ALA2211498	B	Inhibition of EPHB6		1		single protein format	Scientific Literature
8.	ALA2214004	B	Inhibition of EPHB6 assessed as residual activity at 10 uM relative to control		1		single protein format	Scientific Literature
9.	ALA2329865	B	Displacement of ephrin-B1-Fc from EphB6 receptor Fc ectodomain (unknown origin) after 1 hr by ELISA	Homo sapiens	1		single protein format	Scientific Literature
10.	ALA3112111	B	Inhibition of EPHB6 (unknown origin) assessed as residual activity at 10 uM after 1 hr by qPCR analysis relative to control	Homo sapiens	1		single protein format	Scientific Literature
11.	ALA3366570	B	Inhibition of EPHB6 (unknown origin) assessed as residual activity at 10 uM relative to control	Homo sapiens	1		single protein format	Scientific Literature
12.	ALA3738313	B	Displacement of biotinylated ephrin-B1-Fc from EphB6 (unknown origin) preincubated for 1 hr followed by biotinylated-ephrin-B1-Fc addition measured after 4 hrs by ELISA	Homo sapiens	1		single protein format	Scientific Literature
13.	ALA3784722	B	Inhibition of partial length human wild type EPHB6 expressed in mammalian expression system assessed as residual activity at 1 uM relative to control	Homo sapiens	1		assay format	Scientific Literature
14.	ALA3991708	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	237		subcellular format	Kuster lab chemical proteomics drug profiling
15.	ALA4025125	B	Inhibition of wild-type human partial length EPHB6 (Q634 to P948 residues) expressed in mammalian expression system assessed as residual activity at 1 uM by Kinomescan method relative to control	Homo sapiens	1		assay format	Scientific Literature
16.	ALA4043936	B	Inhibition of wild-type human partial length EPHB6 (Q634 to P948 residues) expressed in HEK293 cells assessed as residual activity at 1000 nM after 30 mins by Kinomescan method relative to control	Homo sapiens	1		cell-based format	Scientific Literature
17.	ALA4054968	B	Inhibition of wild-type human partial length EPHB6 (Q634 to P948 residues) expressed in mammalian expression system assessed as residual activity at 50 nM by Kinomescan method relative to control	Homo sapiens	2		assay format	Scientific Literature
18.	ALA4157015	B	Binding affinity to wild-type human partial length EPHB6 (Q634 to P948 residues) expressed in mammalian expression system assessed as residual binding at 1 uM by Kinomescan method relative to control	Homo sapiens	1		assay format	Scientific Literature
19.	ALA4185794	B	Binding affinity to wild-type human partial length EPHB6 (Q634 to P948 residues) expressed in HEK293 cells at 1 uM by Kinomescan method relative to control	Homo sapiens	2		cell-based format	Scientific Literature
20.	ALA4230694	B	Binding affinity to wild-type human partial length EPHB6 (Q634 to P948 residues) expressed in mammalian expression system assessed as residual binding level at 1 uM by Kinomescan method relative to control	Homo sapiens	1		assay format	Scientific Literature