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Assay Detail

CHEMBL5736839

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Binding
Biochemical Assay: The purpose of the CDK6/Cyclin D3 assay is to evaluate the inhibition (% inhibition, Kiapp and Ki values) in the presence of small molecule inhibitors by using a fluorescence based microfluidic mobility shift assay. CDK6/Cyclin D3 catalyses the production of ADP from ATP that accompanies the phosphoryl transfer to the substrate peptide 5-FAM-Dyrktide (5-FAM-RRRFRPASPLRGPPK) (SEQ ID NO:3). The mobility shift assay electrophoretically separates the fluorescently labelled peptides (substrate and phosphorylated product) following the kinase reaction. Both substrate and product are measured and the ratio of these values is used to generate % conversion of substrate to product by the LabChip EZ Reader. Typical reaction solutions contained 2% DMSO (±inhibitor), 2% glycerol, 10 mM MgCl2, 1 mM DTT, 3.5 mM ATP, 0.005% Tween 20 (TW-20), 3 μM 5-FAM-Dyrktide, 4 nM (active sites) activated CDK6/Cyclin D3 in 40 mM HEPES buffer at pH 7.5.
6
Total Activities
2
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 7 — Homologous single protein target
Curated By Autocuration

Target

CDK6/cyclin D1 (CHEMBL2111455)
Type PROTEIN COMPLEX
Organism Homo sapiens

Publication

CDK2 inhibitors
(2021)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 2 6.78 7.23
kon 2 - -
k_off 2 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL6051771 3 7.23
CHEMBL5201870 TEGTOCICLIB 2.0 3 6.33

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL6051771 Ki = 58.6 nM 7.23
CHEMBL5201870 TEGTOCICLIB Ki = 465.0 nM 6.33
CHEMBL5201870 TEGTOCICLIB kon = - -
CHEMBL5201870 TEGTOCICLIB k_off = - s-1 -
CHEMBL6051771 kon = - -
CHEMBL6051771 k_off = - s-1 -