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Assay Detail

CHEMBL3707960

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
In Vitro Kinase Inhibition Assay: In vitro kinase assay analysis may be performed using standard techniques described in the art. These techniques are also used by commercial services providers in order to offer in vitro kinase activity assay services, e.g. the assays offered by Millipore Inc. (worldwide website www(dot)millipore.com), ProQinase GmbH (worldwide website www(dot)proqinase.de) and others. All kinase assays were performed in 96-well FlashPlates from Perkin Elmer/NEN (Boston, Mass., USA) in a 50ul reaction volume. The reaction mixture was pipetted in four steps in the following order: 20ul of assay buffer (standard buffer),5ul of ATP solution (in H2O, 5 ul of test compound (in 10% DMSO), 10ul of substrate/10ul of enzyme solution (premixed)The assay for all enzymes contained 60 mM HEPES-NaOH (pH 7.5), 3 mM MgCl2, 3 mM MnCl2, 3uM Na-Orthovanadate, 1.2 mM DTT, 50 ug/ml PEG2000, 1 uM [33P]-ATP (approx. 5x1005 cpm per well).
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Cyclin-dependent kinase 2 (CHEMBL301)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Inhibitors of protein kinases
(2015)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 6.41 6.78

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3673434 1 6.78
CHEMBL3673435 1 6.04

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3673434 IC50 = 168.0 nM 6.78
CHEMBL3673435 IC50 = 913.0 nM 6.04