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Assay Detail

CHEMBL5356275

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

Binding
Inhibition of TBK1 (unknown origin) incubated for 1 hr in presence of ATP by FRET based Z'-Lyte assay
20
Total Activities
20
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Serine/threonine-protein kinase TBK1 (CHEMBL5408)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Application of deep generative model for design of Pyrrolo[2,3-d] pyrimidine derivatives as new selective TANK binding kinase 1 (TBK1) inhibitors.
Song S, Tang H, Ran T, Fang F, Tong L, Chen H, Xie H, Lu X.
Eur J Med Chem (2023) 247 : 115034 -115034
PubMed 36603506 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 20 7.42 7.65

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5412271 1 7.65
CHEMBL3605057 1 7.64
CHEMBL5438323 1 7.45
CHEMBL5412535 1 7.30
CHEMBL5394835 1 7.27
CHEMBL5401353 1 7.18
CHEMBL5400647 1 -
CHEMBL5431622 1 -
CHEMBL5425152 1 -
CHEMBL5395610 1 -
CHEMBL5403014 1 -
CHEMBL5437308 1 -
CHEMBL5424720 1 -
CHEMBL5411811 1 -
CHEMBL5431220 1 -
CHEMBL5399754 1 -
CHEMBL5400015 1 -
CHEMBL5419757 1 -
CHEMBL5426526 1 -
CHEMBL5423172 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5412271 IC50 = 22.4 nM 7.65
CHEMBL3605057 IC50 = 23.1 nM 7.64
CHEMBL5438323 IC50 = 35.7 nM 7.45
CHEMBL5412535 IC50 = 50.0 nM 7.30
CHEMBL5394835 IC50 = 53.6 nM 7.27
CHEMBL5401353 IC50 = 66.7 nM 7.18
CHEMBL5400647 IC50 - -
CHEMBL5431622 IC50 - -
CHEMBL5425152 IC50 - -
CHEMBL5395610 IC50 - -
CHEMBL5403014 IC50 - -
CHEMBL5437308 IC50 - -
CHEMBL5424720 IC50 - -
CHEMBL5411811 IC50 - -
CHEMBL5431220 IC50 - -
CHEMBL5399754 IC50 - -
CHEMBL5400015 IC50 - -
CHEMBL5419757 IC50 - -
CHEMBL5426526 IC50 - -
CHEMBL5423172 IC50 - -