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Assay Detail

CHEMBL5735124

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

Binding
In Vitro Activity 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.
6
Total Activities
2
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 BTK (CHEMBL5251)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Methods to treat lymphoplasmacytic lymphoma
(2020)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 5.47 5.47
kon 2 - -
k_off 2 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL6038355 3 5.47
CHEMBL5885824 3 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL6038355 IC50 = 3380.0 nM 5.47
CHEMBL6038355 kon = - -
CHEMBL6038355 k_off = - s-1 -
CHEMBL5885824 IC50 > 10000.0 nM -
CHEMBL5885824 kon = - -
CHEMBL5885824 k_off = - s-1 -