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Assay Detail

CHEMBL4771351

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

Binding
Inhibition of human JNK3 after 40 mins by [gamma-33ATP] radiometric assay relative to control
17
Total Activities
17
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

Mitogen-activated protein kinase 10 (CHEMBL2637)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Rational modification, synthesis and biological evaluation of 3,4-dihydroquinoxalin-2(1H)-one derivatives as potent and selective c-Jun N-terminal kinase 3 (JNK3) inhibitors.
Dou X,Huang H,Jiang L,Zhu G,Jin H,Jiao N,Zhang L,Liu Z,Zhang L
Eur J Med Chem (2020) 201 : 112445 -112445
PubMed 32603981 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 6.00 7.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL7064 1 7.05
CHEMBL4795574 1 6.72
CHEMBL4531109 1 6.60
CHEMBL4788894 1 6.50
CHEMBL4777530 1 6.43
CHEMBL4782208 1 6.39
CHEMBL4782076 1 6.37
CHEMBL4800639 1 6.22
CHEMBL4799531 1 5.88
CHEMBL4785607 1 5.84
CHEMBL4794035 1 5.78
CHEMBL4780101 1 5.76
CHEMBL4789089 1 5.46
CHEMBL4793426 1 5.32
CHEMBL4794586 1 5.29
CHEMBL4781949 1 5.25
CHEMBL4776996 1 5.13

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL7064 IC50 = 90.0 nM 7.05
CHEMBL4795574 IC50 = 190.0 nM 6.72
CHEMBL4531109 IC50 = 250.0 nM 6.60
CHEMBL4788894 IC50 = 320.0 nM 6.50
CHEMBL4777530 IC50 = 370.0 nM 6.43
CHEMBL4782208 IC50 = 410.0 nM 6.39
CHEMBL4782076 IC50 = 430.0 nM 6.37
CHEMBL4800639 IC50 = 600.0 nM 6.22
CHEMBL4799531 IC50 = 1330.0 nM 5.88
CHEMBL4785607 IC50 = 1430.0 nM 5.84
CHEMBL4794035 IC50 = 1680.0 nM 5.78
CHEMBL4780101 IC50 = 1750.0 nM 5.76
CHEMBL4789089 IC50 = 3480.0 nM 5.46
CHEMBL4793426 IC50 = 4780.0 nM 5.32
CHEMBL4794586 IC50 = 5150.0 nM 5.29
CHEMBL4781949 IC50 = 5600.0 nM 5.25
CHEMBL4776996 IC50 = 7370.0 nM 5.13