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Assay Detail

CHEMBL5536340

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

Binding
Inhibition of ERK5 in human SN12C cells assessed as luciferase activity by Bright-Glo luminescence assay
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type SN12C
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Mitogen-activated protein kinase 7 (CHEMBL5332)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Imidazopyridine Compounds as ERK5 Inhibitors for Treating Cancer.
Sabnis RW.
ACS Med Chem Lett (2024) 15 : 777 -778
PubMed 38894904 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 8.11 8.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5555328 1 8.30
CHEMBL5573086 1 8.22
CHEMBL5574029 1 8.05
CHEMBL5569331 1 8.05
CHEMBL5571189 1 8.05
CHEMBL5566766 1 8.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5555328 IC50 = 5.0 nM 8.30
CHEMBL5573086 IC50 = 6.0 nM 8.22
CHEMBL5574029 IC50 = 9.0 nM 8.05
CHEMBL5569331 IC50 = 9.0 nM 8.05
CHEMBL5571189 IC50 = 9.0 nM 8.05
CHEMBL5566766 IC50 = 10.0 nM 8.00