Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL3766659

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

Binding
Inhibition of TYK2 in human Jurkat cells assessed as reduction in IL-23-induced luciferase gene expression after 24 hrs
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Structure-Based Design and Synthesis of 3-Amino-1,5-dihydro-4H-pyrazolopyridin-4-one Derivatives as Tyrosine Kinase 2 Inhibitors.
Yogo T, Nagamiya H, Seto M, Sasaki S, Shih-Chung H, Ohba Y, Tokunaga N, Lee GN, Rhim CY, Yoon CH, Cho SY, Skene R, Yamamoto S, Satou Y, Kuno M, Miyazaki T, Nakagawa H, Okabe A, Marui S, Aso K, Yoshida M.
J Med Chem (2016) 59 : 733 -749
PubMed 26701356 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 6.55 7.32

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3763991 1 7.32
CHEMBL3763252 1 7.27
CHEMBL3764277 1 6.96
CHEMBL3764030 1 6.82
CHEMBL3765822 1 6.72
CHEMBL3763213 1 6.70
CHEMBL3765517 1 6.64
CHEMBL3764637 1 6.51
CHEMBL3764383 1 6.36
CHEMBL3764167 1 6.19
CHEMBL3763697 1 5.96
CHEMBL3763184 1 5.16

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3763991 IC50 = 48.0 nM 7.32
CHEMBL3763252 IC50 = 54.0 nM 7.27
CHEMBL3764277 IC50 = 110.0 nM 6.96
CHEMBL3764030 IC50 = 150.0 nM 6.82
CHEMBL3765822 IC50 = 190.0 nM 6.72
CHEMBL3763213 IC50 = 200.0 nM 6.70
CHEMBL3765517 IC50 = 230.0 nM 6.64
CHEMBL3764637 IC50 = 310.0 nM 6.51
CHEMBL3764383 IC50 = 440.0 nM 6.36
CHEMBL3764167 IC50 = 650.0 nM 6.19
CHEMBL3763697 IC50 = 1100.0 nM 5.96
CHEMBL3763184 IC50 = 6900.0 nM 5.16