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Assay Detail

CHEMBL862177

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Binding
Inhibition of JNK1
18
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 Expert

Target

Mitogen-activated protein kinase 8 (CHEMBL2276)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design and synthesis of 2'-anilino-4,4'-bipyridines as selective inhibitors of c-Jun N-terminal kinase-3.
Swahn BM, Xue Y, Arzel E, Kallin E, Magnus A, Plobeck N, Viklund J.
Bioorg Med Chem Lett (2006) 16 : 1397 -1401
PubMed 16337120 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 6.82 7.38

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL380724 1 7.38
CHEMBL203839 2 7.32
CHEMBL202639 1 7.13
CHEMBL203225 1 7.09
CHEMBL206466 1 7.07
CHEMBL202676 1 7.06
CHEMBL203009 1 6.97
CHEMBL203059 1 6.91
CHEMBL202666 1 6.90
CHEMBL205078 1 6.82
CHEMBL204757 1 6.66
CHEMBL205402 1 6.58
CHEMBL203535 1 6.42
CHEMBL379254 1 6.35
CHEMBL380625 1 6.11
CHEMBL203631 1 5.89
CHEMBL383678 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL380724 IC50 = 42.0 nM 7.38
CHEMBL203839 IC50 = 48.0 nM 7.32
CHEMBL203839 IC50 = 55.0 nM 7.26
CHEMBL202639 IC50 = 74.0 nM 7.13
CHEMBL203225 IC50 = 82.0 nM 7.09
CHEMBL206466 IC50 = 85.0 nM 7.07
CHEMBL202676 IC50 = 88.0 nM 7.06
CHEMBL203009 IC50 = 106.0 nM 6.97
CHEMBL203059 IC50 = 122.0 nM 6.91
CHEMBL202666 IC50 = 125.0 nM 6.90
CHEMBL205078 IC50 = 152.0 nM 6.82
CHEMBL204757 IC50 = 219.0 nM 6.66
CHEMBL205402 IC50 = 261.0 nM 6.58
CHEMBL203535 IC50 = 384.0 nM 6.42
CHEMBL379254 IC50 = 451.0 nM 6.35
CHEMBL380625 IC50 = 780.0 nM 6.11
CHEMBL203631 IC50 = 1280.0 nM 5.89
CHEMBL383678 IC50 - -