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Assay Detail

CHEMBL5737853

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Binding
Kinase Inhibitory Activity Assay: The inhibitory activity on a C797S-containing epidermal growth factor receptor (EGFR) kinase and an MET kinase was measured for compound 1 obtained in the above Example, and the results are shown in Table 1 below. The kinase inhibitory activity was measured by the following method:1. Each kinase was incubated with 8 mM MOPS (pH 7.0), 0.2 mM EDTA, 250 μM KKKGQEEEYVFIE (SEQ ID NO: 1), 1 mM sodium orthovanadate, 5 mM sodium-6-glycerophosphate, 10 mM magnesium acetate, and [η-33P]-ATP.2. The compound to be evaluated (DMSO solution) and Mg/ATP were added to proceed the reaction.3. After about 40 minutes at room temperature, the reaction was stopped by the addition of 10 μL of 0.5% phosphoric acid.4. 10 μL of 0.5% reaction solution was spotted onto a P30 filtermat.5. Washed 4 times for about 4 minutes in 0.425% phosphoric acid. Washed once in methanol, and then dried and analyzed by scintillation counting to measure IC50 value.
9
Total Activities
3
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

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

Target

Hepatocyte growth factor receptor (CHEMBL3717)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Pyrimidine derivative having effect of inhibiting cancer cell growth and pharmaceutical composition containing same
(2022)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 7.69 9.00
kon 3 - -
k_off 3 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5596876 3 9.00
CHEMBL3545311 BRIGATINIB 4.0 3 7.16
CHEMBL5597916 3 6.92

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5596876 IC50 = 1.0 nM 9.00
CHEMBL3545311 BRIGATINIB IC50 = 70.0 nM 7.16
CHEMBL5597916 IC50 = 120.0 nM 6.92
CHEMBL5596876 kon = - -
CHEMBL5596876 k_off = - s-1 -
CHEMBL3545311 BRIGATINIB kon = - -
CHEMBL3545311 BRIGATINIB k_off = - s-1 -
CHEMBL5597916 kon = - -
CHEMBL5597916 k_off = - s-1 -