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Assay Detail

CHEMBL4420028

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

Binding
Inhibition of aldehyde oxidase in human liver cytosolic fraction using methyl-nicotinamide substrate incubated for 120 mins by HPLC analysis
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Tissue Liver
Subcellular Cytosolic Fraction
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Aldehyde oxidase (CHEMBL3257)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Therapeutic agent for nonalcoholic fatty liver disease
(2018)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 4.86 7.35

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL81 RALOXIFENE 4.0 1 7.35
CHEMBL276832 HYDRALAZINE 4.0 1 5.41
CHEMBL42 CLOZAPINE 4.0 1 4.36
CHEMBL532 ERYTHROMYCIN 4.0 1 4.01
CHEMBL83 TAMOXIFEN 4.0 1 4.01
CHEMBL590 MENADIONE 4.0 1 4.00
CHEMBL259898 PRASTERONE SULFURIC ACID -1.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL81 RALOXIFENE IC50 = 44.5 nM 7.35
CHEMBL276832 HYDRALAZINE IC50 = 3930.0 nM 5.41
CHEMBL42 CLOZAPINE IC50 = 43300.0 nM 4.36
CHEMBL532 ERYTHROMYCIN IC50 = 96900.0 nM 4.01
CHEMBL83 TAMOXIFEN IC50 = 97300.0 nM 4.01
CHEMBL590 MENADIONE IC50 = 99200.0 nM 4.00
CHEMBL259898 PRASTERONE SULFURIC ACID IC50 > 100000.0 nM -