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Assay Detail

CHEMBL1816569

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

Binding
Inhibition of human recombinant MAOA expressed in insect cells using kynuramine substrate by fluorescence spectroscopy
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 Autocuration

Target

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

Publication

Inhibition of monoamine oxidase by C5-substituted phthalimide analogues.
Manley-King CI, Bergh JJ, Petzer JP.
Bioorg Med Chem (2011) 19 : 4829 -4840
PubMed 21778064 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 5.72 6.66

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1813523 1 6.66
CHEMBL1813522 1 6.04
CHEMBL1813524 1 5.97
CHEMBL1813525 1 5.97
CHEMBL1813520 1 5.76
CHEMBL1813519 1 5.45
CHEMBL342357 1 5.38
CHEMBL1813518 1 5.23
CHEMBL1813521 1 5.05
CHEMBL277294 PHTHALIMIDE 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1813523 IC50 = 220.0 nM 6.66
CHEMBL1813522 IC50 = 920.0 nM 6.04
CHEMBL1813524 IC50 = 1080.0 nM 5.97
CHEMBL1813525 IC50 = 1080.0 nM 5.97
CHEMBL1813520 IC50 = 1730.0 nM 5.76
CHEMBL1813519 IC50 = 3580.0 nM 5.45
CHEMBL342357 IC50 = 4170.0 nM 5.38
CHEMBL1813518 IC50 = 5850.0 nM 5.23
CHEMBL1813521 IC50 = 8990.0 nM 5.05
CHEMBL277294 PHTHALIMIDE IC50 = 165000.0 nM -