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Assay Detail

CHEMBL5738238

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

Binding
Kinase Assay: JAK2 and JAK2 [V617F] Kinase Assay: In 5× Kinase Buffer A, JAK2 or JAK2 [V617F] kinase was mixed with pre-diluted compounds at different concentrations in duplicate for 10 minutes. The corresponding substrate and ATP were added and reacted at room temperature for 20 minutes (in which negative and positive controls were set: the negative control was a blank control and the positive control was erlotinib). After the reaction was completed, a detection reagent (the reagent in the HTRF Kinase TK kit) was added. After incubation at room temperature for 30 minutes, the enzyme activities in the presence of the compounds disclosed herein at each concentration were measured by an Evnvision microplate reader, and inhibitory activities of compounds at different concentrations on the enzyme activity were calculated. The inhibitory activities of compounds at different concentrations on enzyme activity were then fitted according to the four-parameter equation using Graphpad 5.0 software, and the IC50 values were calculated.
18
Total Activities
1
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

Tyrosine-protein kinase JAK2 (CHEMBL2971)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Diphenylaminopyrimidine compound for inhibiting kinase activity
(2022)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 8.50 8.54
kon 6 - -
k_off 6 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1287853 FEDRATINIB 4.0 18 8.54

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1287853 FEDRATINIB IC50 = 2.89 nM 8.54
CHEMBL1287853 FEDRATINIB IC50 = 3.08 nM 8.51
CHEMBL1287853 FEDRATINIB IC50 = 3.06 nM 8.51
CHEMBL1287853 FEDRATINIB IC50 = 3.16 nM 8.50
CHEMBL1287853 FEDRATINIB IC50 = 3.24 nM 8.49
CHEMBL1287853 FEDRATINIB IC50 = 3.47 nM 8.46
CHEMBL1287853 FEDRATINIB kon = - -
CHEMBL1287853 FEDRATINIB k_off = - s-1 -
CHEMBL1287853 FEDRATINIB kon = - -
CHEMBL1287853 FEDRATINIB k_off = - s-1 -
CHEMBL1287853 FEDRATINIB kon = - -
CHEMBL1287853 FEDRATINIB k_off = - s-1 -
CHEMBL1287853 FEDRATINIB kon = - -
CHEMBL1287853 FEDRATINIB k_off = - s-1 -
CHEMBL1287853 FEDRATINIB kon = - -
CHEMBL1287853 FEDRATINIB k_off = - s-1 -
CHEMBL1287853 FEDRATINIB kon = - -
CHEMBL1287853 FEDRATINIB k_off = - s-1 -