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Assay Detail

CHEMBL4257308

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

Binding
Inhibition of N-terminal His6-Smt3-fusion tagged human Usp9x catalytic domain (1553 to 1960 residues) expressed in Escherichia coli pre- incubated for 30 mins before Ub-AMC substrate addition by fluorescence based assay
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Intermediate

Target

Ubiquitin carboxyl-terminal hydrolase 9X (CHEMBL2406899)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Deubiquitinase inhibitors and methods for use of the same
(2016)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 5.40 5.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4279461 1 5.92
CHEMBL4287357 1 5.80
CHEMBL4278343 1 5.70
CHEMBL4293176 1 5.34
CHEMBL1923233 1 5.32
CHEMBL4292817 1 5.29
CHEMBL4283401 1 5.22
CHEMBL4291403 1 5.21
CHEMBL4277327 1 5.21
CHEMBL4279846 1 4.97

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4279461 IC50 = 1200.0 nM 5.92
CHEMBL4287357 IC50 = 1600.0 nM 5.80
CHEMBL4278343 IC50 = 1990.0 nM 5.70
CHEMBL4293176 IC50 = 4610.0 nM 5.34
CHEMBL1923233 IC50 = 4800.0 nM 5.32
CHEMBL4292817 IC50 = 5120.0 nM 5.29
CHEMBL4283401 IC50 = 5970.0 nM 5.22
CHEMBL4291403 IC50 = 6230.0 nM 5.21
CHEMBL4277327 IC50 = 6130.0 nM 5.21
CHEMBL4279846 IC50 = 10730.0 nM 4.97