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Assay Detail

CHEMBL1811056

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

Binding
Inhibition of CDK2
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Discovery of novel imidazo[1,2-a]pyridines as inhibitors of the insulin-like growth factor-1 receptor tyrosine kinase.
Ducray R, Simpson I, Jung FH, Nissink JW, Kenny PW, Fitzek M, Walker GE, Ward LT, Hudson K.
Bioorg Med Chem Lett (2011) 21 : 4698 -4701
PubMed 21775140 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 5.81 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL73303 1 9.00
CHEMBL1809191 1 7.11
CHEMBL1809044 1 5.96
CHEMBL1809194 1 5.96
CHEMBL1809193 1 5.57
CHEMBL1809195 1 5.00
CHEMBL1809196 1 4.80
CHEMBL1806525 1 4.57
CHEMBL1809197 1 4.28
CHEMBL1809192 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL73303 IC50 = 1.0 nM 9.00
CHEMBL1809191 IC50 = 78.0 nM 7.11
CHEMBL1809044 IC50 = 1100.0 nM 5.96
CHEMBL1809194 IC50 = 1100.0 nM 5.96
CHEMBL1809193 IC50 = 2700.0 nM 5.57
CHEMBL1809195 IC50 = 10000.0 nM 5.00
CHEMBL1809196 IC50 = 16000.0 nM 4.80
CHEMBL1806525 IC50 = 27000.0 nM 4.57
CHEMBL1809197 IC50 = 53000.0 nM 4.28
CHEMBL1809192 IC50 > 100000.0 nM -