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Assay Detail

CHEMBL3395898

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

Binding
Inhibition of JNK3 (unknown origin) by time-resolved fluorescence assay
17
Total Activities
17
Compounds Tested
2
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

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 16 7.76 9.80
Ki 1 6.89 6.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3220502 1 9.80
CHEMBL3220493 1 9.52
CHEMBL3220495 1 9.10
CHEMBL571626 1 8.40
CHEMBL3393599 1 8.15
CHEMBL1233748 1 8.05
CHEMBL1233747 1 7.60
CHEMBL3393595 1 7.50
CHEMBL3393598 1 7.40
CHEMBL3220466 1 7.08
CHEMBL3393596 1 7.07
CHEMBL1725279 SP-600125 1 7.05
CHEMBL2376930 1 6.92
CHEMBL3393597 1 6.89
CHEMBL571619 1 6.89
CHEMBL585951 1 6.83
CHEMBL2144409 1 6.80

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3220502 IC50 = 0.16 nM 9.80
CHEMBL3220493 IC50 = 0.3 nM 9.52
CHEMBL3220495 IC50 = 0.8 nM 9.10
CHEMBL571626 IC50 = 4.0 nM 8.40
CHEMBL3393599 IC50 = 7.0 nM 8.15
CHEMBL1233748 IC50 = 9.0 nM 8.05
CHEMBL1233747 IC50 = 25.0 nM 7.60
CHEMBL3393595 IC50 = 32.0 nM 7.50
CHEMBL3393598 IC50 = 40.0 nM 7.40
CHEMBL3220466 IC50 = 83.0 nM 7.08
CHEMBL3393596 IC50 = 85.0 nM 7.07
CHEMBL1725279 SP-600125 IC50 = 90.0 nM 7.05
CHEMBL2376930 IC50 = 120.0 nM 6.92
CHEMBL3393597 IC50 = 129.0 nM 6.89
CHEMBL571619 Ki = 130.0 nM 6.89
CHEMBL585951 IC50 = 148.0 nM 6.83
CHEMBL2144409 IC50 = 159.0 nM 6.80