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Assay Detail

CHEMBL3404560

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

Binding
Inhibition of human recombinant MAOA using kynuramine substrate assessed as reduction in MAO-generated 4-hydroxyquinoline level by fluorescence spectrophotometry
11
Total Activities
11
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

Amine oxidase [flavin-containing] A (CHEMBL1951)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

The synthesis and evaluation of sesamol and benzodioxane derivatives as inhibitors of monoamine oxidase.
Engelbrecht I, Petzer JP, Petzer A.
Bioorg Med Chem Lett (2015) 25 : 1896 -1900
PubMed 25857942 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 4.64 7.16

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL191083 METHYLENE BLUE CATION 4.0 1 7.16
CHEMBL3402196 1 4.88
CHEMBL3402197 1 4.77
CHEMBL3402198 1 4.56
CHEMBL3402195 1 4.44
CHEMBL3402190 1 4.42
CHEMBL3402189 1 4.29
CHEMBL3402200 1 4.16
CHEMBL3402199 1 4.15
CHEMBL3400170 1 4.11
CHEMBL3402191 1 4.06

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL191083 METHYLENE BLUE CATION IC50 = 70.0 nM 7.16
CHEMBL3402196 IC50 = 13200.0 nM 4.88
CHEMBL3402197 IC50 = 16900.0 nM 4.77
CHEMBL3402198 IC50 = 27800.0 nM 4.56
CHEMBL3402195 IC50 = 36000.0 nM 4.44
CHEMBL3402190 IC50 = 38400.0 nM 4.42
CHEMBL3402189 IC50 = 51800.0 nM 4.29
CHEMBL3402200 IC50 = 69400.0 nM 4.16
CHEMBL3402199 IC50 = 70400.0 nM 4.15
CHEMBL3400170 IC50 = 77100.0 nM 4.11
CHEMBL3402191 IC50 = 87700.0 nM 4.06