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Assay Detail

CHEMBL3787909

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

Binding
Inhibition of human recombinant MAO-B using kynuramine as substrate after 30 mins by fluorescence spectrophotometry
13
Total Activities
13
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] B (CHEMBL2039)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and evaluation of 4-hydroxyl aurone derivatives as multifunctional agents for the treatment of Alzheimer's disease.
Li Y, Qiang X, Luo L, Li Y, Xiao G, Tan Z, Deng Y.
Bioorg Med Chem (2016) 24 : 2342 -2351
PubMed 27079124 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 6.07 7.08

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL887 RASAGILINE 4.0 1 7.08
CHEMBL3786378 1 6.65
CHEMBL3786747 1 6.48
CHEMBL1814450 1 6.47
CHEMBL3786282 1 6.41
CHEMBL3263556 1 6.41
CHEMBL3785406 1 6.15
CHEMBL3786785 1 6.09
CHEMBL3786723 1 5.82
CHEMBL92401 IPRONIAZID 2.0 1 5.71
CHEMBL8706 CLORGILINE 2.0 1 5.38
CHEMBL2288402 1 5.23
CHEMBL3787128 1 4.97

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL887 RASAGILINE IC50 = 82.5 nM 7.08
CHEMBL3786378 IC50 = 226.0 nM 6.65
CHEMBL3786747 IC50 = 334.0 nM 6.48
CHEMBL1814450 IC50 = 340.0 nM 6.47
CHEMBL3786282 IC50 = 391.0 nM 6.41
CHEMBL3263556 IC50 = 393.0 nM 6.41
CHEMBL3785406 IC50 = 703.0 nM 6.15
CHEMBL3786785 IC50 = 808.0 nM 6.09
CHEMBL3786723 IC50 = 1500.0 nM 5.82
CHEMBL92401 IPRONIAZID IC50 = 1950.0 nM 5.71
CHEMBL8706 CLORGILINE IC50 = 4190.0 nM 5.38
CHEMBL2288402 IC50 = 5940.0 nM 5.23
CHEMBL3787128 IC50 = 10800.0 nM 4.97