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Assay Detail

CHEMBL3395896

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

Binding
Inhibition of JNK1 (unknown origin) by time-resolved fluorescence assay
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 8 (CHEMBL2276)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Inhibitors of c-Jun N-terminal kinases: an update.
Koch P, Gehringer M, Laufer SA.
J Med Chem (2015) 58 : 72 -95
PubMed 25415535 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 7.46 9.62

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3220502 1 9.62
CHEMBL3393600 1 9.10
CHEMBL3220493 1 9.00
CHEMBL3220495 1 8.52
CHEMBL571626 1 7.80
CHEMBL3393599 1 7.77
CHEMBL1725279 SP-600125 1 7.40
CHEMBL1761554 1 7.30
CHEMBL2144409 1 7.17
CHEMBL1233748 1 7.14
CHEMBL3393596 1 7.13
CHEMBL3393595 1 7.00
CHEMBL585951 1 7.00
CHEMBL3393597 1 6.78
CHEMBL1233747 1 6.40
CHEMBL3393598 1 6.01
CHEMBL2376930 1 5.64

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3220502 IC50 = 0.24 nM 9.62
CHEMBL3393600 IC50 = 0.8 nM 9.10
CHEMBL3220493 IC50 = 1.0 nM 9.00
CHEMBL3220495 IC50 = 3.0 nM 8.52
CHEMBL571626 IC50 = 16.0 nM 7.80
CHEMBL3393599 IC50 = 17.0 nM 7.77
CHEMBL1725279 SP-600125 IC50 = 40.0 nM 7.40
CHEMBL1761554 IC50 = 50.0 nM 7.30
CHEMBL2144409 IC50 = 67.0 nM 7.17
CHEMBL1233748 IC50 = 73.0 nM 7.14
CHEMBL3393596 IC50 = 74.0 nM 7.13
CHEMBL3393595 IC50 = 101.0 nM 7.00
CHEMBL585951 IC50 = 99.0 nM 7.00
CHEMBL3393597 IC50 = 166.0 nM 6.78
CHEMBL1233747 IC50 = 400.0 nM 6.40
CHEMBL3393598 IC50 = 970.0 nM 6.01
CHEMBL2376930 IC50 = 2300.0 nM 5.64