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Results: 1 to 20 of 23548

1.

Competitive binding affinity to HUNK (unknown origin) assessed as enzyme remaining bound to anchored active-site ligand at 10 uM relative to control

Source:
ChEMBL
Protein Target:
Hormonally up-regulated neu tumor-associated kinase; B19; Serine/threonine-protein kinase MAK-V
2.

Binding constant for HUNK kinase domain [Confirmatory]

Source:
ChEMBL
Protein Target:
Hormonally up-regulated neu tumor-associated kinase; B19; Serine/threonine-protein kinase MAK-V
3.

Inhibition of MARK1 (unknown origin) at 1 uM in presence of 100 uM ATP

Source:
ChEMBL
Protein Target:
Serine/threonine-protein kinase MARK1; MAP/microtubule affinity-regulating kinase 1; PAR1 homolog c; Par-1c; Par1c
4.

Inhibition of MARK1 (unknown origin) at 100 nM

Source:
ChEMBL
Protein Target:
Serine/threonine-protein kinase MARK1; MAP/microtubule affinity-regulating kinase 1; PAR1 homolog c; Par-1c; Par1c
5.

Inhibition of MARK1 (unknown origin) at 1 uM relative to control

Source:
ChEMBL
Protein Target:
Serine/threonine-protein kinase MARK1; MAP/microtubule affinity-regulating kinase 1; PAR1 homolog c; Par-1c; Par1c
6.

Inhibition of MARK1 kinase (unknown origin) at 1 uM

Source:
ChEMBL
Protein Target:
Serine/threonine-protein kinase MARK1; MAP/microtubule affinity-regulating kinase 1; PAR1 homolog c; Par-1c; Par1c
7.

Inhibition of human MARK1 assessed as enzyme activity at 1 uM relative to control

Source:
ChEMBL
Protein Target:
Serine/threonine-protein kinase MARK1; MAP/microtubule affinity-regulating kinase 1; PAR1 homolog c; Par-1c; Par1c
8.

Inhibition of human MARK1 [Confirmatory]

Source:
ChEMBL
Protein Target:
Serine/threonine-protein kinase MARK1; MAP/microtubule affinity-regulating kinase 1; PAR1 homolog c; Par-1c; Par1c
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