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Assay Detail

CHEMBL962088

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

Binding
Inhibition of human recombinant Aurora B
7
Total Activities
7
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

Aurora kinase B (CHEMBL2185)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis, and biological evaluation of novel 3-aryl-4-(1H-indole-3yl)-1,5-dihydro-2H-pyrrole-2-ones as vascular endothelial growth factor receptor (VEGF-R) inhibitors.
Peifer C, Selig R, Kinkel K, Ott D, Totzke F, Schächtele C, Heidenreich R, Röcken M, Schollmeyer D, Laufer S.
J Med Chem (2008) 51 : 3814 -3824
PubMed 18529047 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 4.88 5.68

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL521201 1 5.68
CHEMBL452812 1 5.31
CHEMBL509435 1 5.01
CHEMBL201511 MALEIMIDE 1 4.77
CHEMBL488811 1 4.70
CHEMBL488646 1 4.37
CHEMBL529663 1 4.34

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL521201 IC50 = 2100.0 nM 5.68
CHEMBL452812 IC50 = 4900.0 nM 5.31
CHEMBL509435 IC50 = 9800.0 nM 5.01
CHEMBL201511 MALEIMIDE IC50 = 17000.0 nM 4.77
CHEMBL488811 IC50 = 20000.0 nM 4.70
CHEMBL488646 IC50 = 43000.0 nM 4.37
CHEMBL529663 IC50 = 46000.0 nM 4.34