Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL3803166

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

Binding
Inhibition of CDK2 (unknown origin)
8
Total Activities
8
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

Discovery of a Selective and Potent Inhibitor of Mitogen-Activated Protein Kinase-Interacting Kinases 1 and 2 (MNK1/2) Utilizing Structure-Based Drug Design.
Han W, Ding Y, Xu Y, Pfister K, Zhu S, Warne B, Doyle M, Aikawa M, Amiri P, Appleton B, Stuart DD, Fanidi A, Shafer CM.
J Med Chem (2016) 59 : 3034 -3045
PubMed 27002243 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 5.34 5.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3799935 1 5.89
CHEMBL3798762 1 5.85
CHEMBL3797873 1 5.47
CHEMBL3797828 1 5.40
CHEMBL3797574 1 5.24
CHEMBL3798066 1 4.96
CHEMBL3797559 1 4.60
CHEMBL3800585 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3799935 IC50 = 1300.0 nM 5.89
CHEMBL3798762 IC50 = 1400.0 nM 5.85
CHEMBL3797873 IC50 = 3400.0 nM 5.47
CHEMBL3797828 IC50 = 4000.0 nM 5.40
CHEMBL3797574 IC50 = 5700.0 nM 5.24
CHEMBL3798066 IC50 = 11000.0 nM 4.96
CHEMBL3797559 IC50 = 25000.0 nM 4.60
CHEMBL3800585 IC50 > 25000.0 nM -