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

CHEMBL1071576

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

Binding
Inhibition of wild-type JNK2 by isothermal calorimetry
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Mitogen-activated protein kinase 9 (CHEMBL4179)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and optimization of thiadiazole derivatives as a novel class of substrate competitive c-Jun N-terminal kinase inhibitors.
De SK, Chen V, Stebbins JL, Chen LH, Cellitti JF, Machleidt T, Barile E, Riel-Mehan M, Dahl R, Yang L, Emdadi A, Murphy R, Pellecchia M.
Bioorg Med Chem (2010) 18 : 590 -596
PubMed 20045647 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 3 5.22 5.55

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL611079 1 5.55
CHEMBL508280 1 5.09
CHEMBL609039 1 5.03

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL611079 Kd = 2800.0 nM 5.55
CHEMBL508280 Kd = 8100.0 nM 5.09
CHEMBL609039 Kd = 9400.0 nM 5.03