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Assay Detail

CHEMBL5733424

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

Binding
Inhibition Assay: The in vitro activity of the compounds described herein in inhibiting TAK1, HCK, and other kinases were obtained using an Invitrogen Select Screening assay as known in the art.
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

Hexokinase-4 (CHEMBL3820)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Methods to treat lymphoplasmacytic lymphoma
(2018)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 5.09 5.09
kon 3 - -
k_off 3 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5950918 3 5.09
CHEMBL5994443 3 -
CHEMBL6014241 3 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5950918 IC50 = 8210.0 nM 5.09
CHEMBL5950918 kon = - -
CHEMBL5950918 k_off = - s-1 -
CHEMBL5994443 IC50 > 10000.0 nM -
CHEMBL5994443 kon = - -
CHEMBL5994443 k_off = - s-1 -
CHEMBL6014241 IC50 > 3330.0 nM -
CHEMBL6014241 kon = - -
CHEMBL6014241 k_off = - s-1 -