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Assay Detail

CHEMBL897015

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Binding
Inhibition of CDK2
22
Total Activities
22
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

3-Hydroxychromones as cyclin-dependent kinase inhibitors: synthesis and biological evaluation.
Lee J, Park T, Jeong S, Kim KH, Hong C.
Bioorg Med Chem Lett (2007) 17 : 1284 -1287
PubMed 17178224 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 22 5.89 7.25

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL232556 1 7.25
CHEMBL392776 1 7.12
CHEMBL232557 1 7.06
CHEMBL392775 1 6.72
CHEMBL232749 1 6.60
CHEMBL232123 1 6.20
CHEMBL232737 1 6.19
CHEMBL233152 1 5.85
CHEMBL232743 1 5.82
CHEMBL232934 1 5.80
CHEMBL231928 1 5.80
CHEMBL233153 1 5.77
CHEMBL232736 1 5.58
CHEMBL232735 1 5.52
CHEMBL232353 1 5.40
CHEMBL122701 1 5.40
CHEMBL232939 1 5.36
CHEMBL31574 FISETIN 2.0 1 5.30
CHEMBL151 LUTEOLIN 2.0 1 4.70
CHEMBL50 QUERCETIN 3.0 1 4.40
CHEMBL222541 1 -
CHEMBL222556 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL232556 IC50 = 56.0 nM 7.25
CHEMBL392776 IC50 = 75.0 nM 7.12
CHEMBL232557 IC50 = 87.0 nM 7.06
CHEMBL392775 IC50 = 190.0 nM 6.72
CHEMBL232749 IC50 = 250.0 nM 6.60
CHEMBL232123 IC50 = 630.0 nM 6.20
CHEMBL232737 IC50 = 640.0 nM 6.19
CHEMBL233152 IC50 = 1400.0 nM 5.85
CHEMBL232743 IC50 = 1500.0 nM 5.82
CHEMBL232934 IC50 = 1600.0 nM 5.80
CHEMBL231928 IC50 = 1600.0 nM 5.80
CHEMBL233153 IC50 = 1700.0 nM 5.77
CHEMBL232736 IC50 = 2600.0 nM 5.58
CHEMBL232735 IC50 = 3000.0 nM 5.52
CHEMBL232353 IC50 = 4000.0 nM 5.40
CHEMBL122701 IC50 = 4000.0 nM 5.40
CHEMBL232939 IC50 = 4400.0 nM 5.36
CHEMBL31574 FISETIN IC50 = 5000.0 nM 5.30
CHEMBL151 LUTEOLIN IC50 = 20000.0 nM 4.70
CHEMBL50 QUERCETIN IC50 = 40000.0 nM 4.40
CHEMBL222541 IC50 > 500000.0 nM -
CHEMBL222556 IC50 > 500000.0 nM -