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Assay Detail

CHEMBL5733653

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Binding
Inhibition Assay: CDK-2/cyclin A (5-20 mU diluted in 50 mM Hepes pH 7.5, 1 mM DTT, 0.02% Brij35, 100 mM NaCl) was assayed against Histone H1 in a final volume of 25.5 μl containing 50 mM Hepes pH7.5, 1 mM DTT, 0.02% Brij35, 100 mM NaCl, Histone H1 (1 mg/ml), 10 mM magnesium acetate and 0.02 mM [33P-g-ATP](500-1000 cpm/pmole) and incubated for 30 min at room temperature. Assays were stopped by addition of 5 μl of 0.5 M (3%) orthophosphoric acid and then harvested onto P81 Unifilter plates with a wash buffer of 50 mM orthophosphoric acid.
15
Total Activities
5
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

CDK2/Cyclin A2 (CHEMBL3038469)
Type PROTEIN COMPLEX
Organism Homo sapiens

Publication

Rohitukine analogs as cyclin-dependent kinase inhibitors and a process for the preparation thereof
(2018)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 6.78 7.80
kon 5 - -
k_off 5 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5788329 3 7.80
CHEMBL422897 3 6.77
CHEMBL5746046 3 6.33
CHEMBL6008368 3 6.22
CHEMBL6036038 3 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5788329 IC50 = 16.0 nM 7.80
CHEMBL422897 IC50 = 170.0 nM 6.77
CHEMBL5746046 IC50 = 466.0 nM 6.33
CHEMBL6008368 IC50 = 608.0 nM 6.22
CHEMBL6036038 IC50 > 10000.0 nM -
CHEMBL6036038 kon = - -
CHEMBL6036038 k_off = - s-1 -
CHEMBL422897 kon = - -
CHEMBL422897 k_off = - s-1 -
CHEMBL5788329 kon = - -
CHEMBL5788329 k_off = - s-1 -
CHEMBL6008368 kon = - -
CHEMBL6008368 k_off = - s-1 -
CHEMBL5746046 kon = - -
CHEMBL5746046 k_off = - s-1 -