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Assay Detail

CHEMBL5729909

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Binding
Kinase Inhibition Assay: Preparation of AKT1 and AKT2 and measurement of in vitro inhibitory activity of the above-mentioned compounds against AKT1 and AKT2 kinase activity were carried out with reference to the method disclosed in Biochem. J. Vol. 385, pp 399-408 (2005). In the preparation of AKT1 and AKT2, human AKT1 and AKT2 to which a middle T antigen tag was added were expressed in Sf 9 insect cells, and then AKT1 and AKT2 were prepared following affinity purification and activation by PDK1. The prepared AKT1 and AKT2 were stored at â 80C. until the time of measurement of inhibitory activity of the compounds. In the measurement of inhibitory activity of the compounds, AKT1 or AKT2 and each compound of the present invention were preincubated at 25C. for 120 minutes in a buffer solution for reaction (15 mM Tris-HCl pH 7.5, 0.01% Tween-20, 2 mM DTT). As a substrate, biotinylated Crosstide (bioton-KGSGSGRPRTSSFAEG), MgCl2, and ATP were added to final concentrations.
192
Total Activities
64
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

RAC-alpha serine/threonine-protein kinase (CHEMBL4282)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Imidazo-oxazine compound or salt thereof
(2014)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 64 8.25 9.10
kon 64 - -
k_off 64 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3701762 3 9.10
CHEMBL3701776 3 8.89
CHEMBL3701763 3 8.89
CHEMBL3701753 3 8.85
CHEMBL3701752 3 8.85
CHEMBL3701766 3 8.82
CHEMBL3701749 3 8.80
CHEMBL3701767 3 8.80
CHEMBL3701775 3 8.74
CHEMBL3701733 3 8.74
CHEMBL3701770 3 8.74
CHEMBL3701769 3 8.74
CHEMBL3701750 3 8.70
CHEMBL3701773 3 8.68
CHEMBL3701758 3 8.66
CHEMBL3701726 3 8.64
CHEMBL3701774 3 8.62
CHEMBL3701735 3 8.54
CHEMBL3701772 3 8.51
CHEMBL3701778 3 8.51
CHEMBL3701717 3 8.43
CHEMBL3701734 3 8.43
CHEMBL3701754 3 8.41
CHEMBL3701727 3 8.41
CHEMBL5316198 3 8.38
CHEMBL3701761 3 8.36
CHEMBL3701768 3 8.36
CHEMBL3701718 3 8.34
CHEMBL3701732 3 8.32
CHEMBL3701777 3 8.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3701762 IC50 = 0.8 nM 9.10
CHEMBL3701763 IC50 = 1.3 nM 8.89
CHEMBL3701776 IC50 = 1.3 nM 8.89
CHEMBL3701753 IC50 = 1.4 nM 8.85
CHEMBL3701752 IC50 = 1.4 nM 8.85
CHEMBL3701766 IC50 = 1.5 nM 8.82
CHEMBL3701749 IC50 = 1.6 nM 8.80
CHEMBL3701767 IC50 = 1.6 nM 8.80
CHEMBL3701733 IC50 = 1.8 nM 8.74
CHEMBL3701769 IC50 = 1.8 nM 8.74
CHEMBL3701770 IC50 = 1.8 nM 8.74
CHEMBL3701775 IC50 = 1.8 nM 8.74
CHEMBL3701750 IC50 = 2.0 nM 8.70
CHEMBL3701773 IC50 = 2.1 nM 8.68
CHEMBL3701758 IC50 = 2.2 nM 8.66
CHEMBL3701726 IC50 = 2.3 nM 8.64
CHEMBL3701774 IC50 = 2.4 nM 8.62
CHEMBL3701735 IC50 = 2.9 nM 8.54
CHEMBL3701778 IC50 = 3.1 nM 8.51
CHEMBL3701772 IC50 = 3.1 nM 8.51
CHEMBL3701717 IC50 = 3.7 nM 8.43
CHEMBL3701734 IC50 = 3.7 nM 8.43
CHEMBL3701754 IC50 = 3.9 nM 8.41
CHEMBL3701727 IC50 = 3.9 nM 8.41
CHEMBL5316198 IC50 = 4.2 nM 8.38
CHEMBL3701768 IC50 = 4.4 nM 8.36
CHEMBL3701761 IC50 = 4.4 nM 8.36
CHEMBL3701718 IC50 = 4.6 nM 8.34
CHEMBL3701732 IC50 = 4.8 nM 8.32
CHEMBL3701777 IC50 = 5.0 nM 8.30
CHEMBL3701728 IC50 = 5.3 nM 8.28
CHEMBL3701755 IC50 = 5.4 nM 8.27
CHEMBL3701751 IC50 = 5.5 nM 8.26
CHEMBL3701765 IC50 = 5.5 nM 8.26
CHEMBL3701736 IC50 = 6.0 nM 8.22
CHEMBL3701760 IC50 = 6.2 nM 8.21
CHEMBL3701756 IC50 = 6.4 nM 8.19
CHEMBL3701724 IC50 = 6.4 nM 8.19
CHEMBL3701747 IC50 = 6.6 nM 8.18
CHEMBL3701720 IC50 = 7.1 nM 8.15
CHEMBL3701757 IC50 = 8.0 nM 8.10
CHEMBL3701737 IC50 = 8.2 nM 8.09
CHEMBL3701725 IC50 = 8.5 nM 8.07
CHEMBL3701759 IC50 = 8.6 nM 8.07
CHEMBL3701722 IC50 = 9.8 nM 8.01
CHEMBL3701742 IC50 = 11.0 nM 7.96
CHEMBL5316199 IC50 = 11.0 nM 7.96
CHEMBL3701743 IC50 = 11.0 nM 7.96
CHEMBL3701740 IC50 = 12.0 nM 7.92
CHEMBL3701746 IC50 = 12.0 nM 7.92