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Assay Detail

CHEMBL3391341

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

Binding
Inhibition of LIMK2 (unknown origin)
8
Total Activities
8
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

LIM domain kinase 2 (CHEMBL5932)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Development of substituted 7-phenyl-4-aminobenzothieno[3,2-d] pyrimidines as potent LIMK1 inhibitors
Sleebs BE, Ganame D, Levit A, Street IP, Gregg A, Falk H, Baell JB
Medchemcomm (2011) 2 : 982 -986
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 6.79 7.07

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2141887 1 7.07
CHEMBL3347507 1 7.05
CHEMBL3347669 1 6.99
CHEMBL3347513 1 6.88
CHEMBL3347683 1 6.80
CHEMBL3347528 1 6.79
CHEMBL3347689 1 6.56
CHEMBL2070615 1 6.16

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2141887 IC50 = 85.0 nM 7.07
CHEMBL3347507 IC50 = 90.0 nM 7.05
CHEMBL3347669 IC50 = 103.0 nM 6.99
CHEMBL3347513 IC50 = 133.0 nM 6.88
CHEMBL3347683 IC50 = 157.0 nM 6.80
CHEMBL3347528 IC50 = 164.0 nM 6.79
CHEMBL3347689 IC50 = 273.0 nM 6.56
CHEMBL2070615 IC50 = 696.0 nM 6.16