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Assay Detail

CHEMBL3625900

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

Binding
Inhibition of Tyk2 (unknown origin) using 25 uM of ATP and Tyr3 peptide by Z'-LYTE kinase assay
18
Total Activities
18
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

Non-receptor tyrosine-protein kinase TYK2 (CHEMBL3553)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Benzimidazole Derivatives as Potent JAK1-Selective Inhibitors.
Kim MK, Shin H, Park KS, Kim H, Park J, Kim K, Nam J, Choo H, Chong Y.
J Med Chem (2015) 58 : 7596 -7602
PubMed 26351728 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 5.60 8.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL21156 1 8.30
CHEMBL3622825 1 5.60
CHEMBL3622830 1 5.60
CHEMBL3622823 1 5.57
CHEMBL3622832 1 5.57
CHEMBL3622838 1 5.55
CHEMBL3622824 1 5.51
CHEMBL3622833 1 5.50
CHEMBL3622834 1 5.50
CHEMBL3622827 1 5.48
CHEMBL3622831 1 5.46
CHEMBL3622826 1 5.43
CHEMBL3622835 1 5.43
CHEMBL3622828 1 5.38
CHEMBL3622837 1 5.37
CHEMBL3622836 1 5.24
CHEMBL3622822 1 5.19
CHEMBL3622829 1 5.12

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL21156 IC50 = 5.0 nM 8.30
CHEMBL3622825 IC50 = 2500.0 nM 5.60
CHEMBL3622830 IC50 = 2500.0 nM 5.60
CHEMBL3622823 IC50 = 2700.0 nM 5.57
CHEMBL3622832 IC50 = 2700.0 nM 5.57
CHEMBL3622838 IC50 = 2800.0 nM 5.55
CHEMBL3622824 IC50 = 3100.0 nM 5.51
CHEMBL3622833 IC50 = 3200.0 nM 5.50
CHEMBL3622834 IC50 = 3200.0 nM 5.50
CHEMBL3622827 IC50 = 3300.0 nM 5.48
CHEMBL3622831 IC50 = 3500.0 nM 5.46
CHEMBL3622826 IC50 = 3700.0 nM 5.43
CHEMBL3622835 IC50 = 3700.0 nM 5.43
CHEMBL3622828 IC50 = 4200.0 nM 5.38
CHEMBL3622837 IC50 = 4300.0 nM 5.37
CHEMBL3622836 IC50 = 5800.0 nM 5.24
CHEMBL3622822 IC50 = 6400.0 nM 5.19
CHEMBL3622829 IC50 = 7500.0 nM 5.12