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Assay Detail

CHEMBL2433712

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

Binding
Inhibition of recombinant human MAO-A assessed as inhibition of kynuramine conversion to fluorescent metabolite 4-hydroxyquinoline after 20 mins 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

Inhibition of monoamine oxidase by 3,4-dihydro-2(1H)-quinolinone derivatives.
Meiring L, Petzer JP, Petzer A.
Bioorg Med Chem Lett (2013) 23 : 5498 -5502
PubMed 24012182 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 4.58 5.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2430707 1 5.10
CHEMBL2430703 1 4.91
CHEMBL2430705 1 4.71
CHEMBL2430709 1 4.65
CHEMBL2430704 1 4.65
CHEMBL172856 1 4.60
CHEMBL2430702 1 4.30
CHEMBL2430708 1 4.27
CHEMBL145059 1 4.04
CHEMBL2430711 1 -
CHEMBL2430710 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2430707 IC50 = 7980.0 nM 5.10
CHEMBL2430703 IC50 = 12400.0 nM 4.91
CHEMBL2430705 IC50 = 19700.0 nM 4.71
CHEMBL2430709 IC50 = 22500.0 nM 4.65
CHEMBL2430704 IC50 = 22500.0 nM 4.65
CHEMBL172856 IC50 = 25300.0 nM 4.60
CHEMBL2430702 IC50 = 50600.0 nM 4.30
CHEMBL2430708 IC50 = 53700.0 nM 4.27
CHEMBL145059 IC50 = 90400.0 nM 4.04
CHEMBL2430711 IC50 = 183000.0 nM -
CHEMBL2430710 IC50 = 161000.0 nM -