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Assay Detail

CHEMBL4221599

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

Binding
Inhibition of recombinant human MAO-B using kynuramine as substrate after 30 mins by fluorescence assay
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

Multifunctional 5,6-dimethoxybenzo[d]isothiazol-3(2H)-one-N-alkylbenzylamine derivatives with acetylcholinesterase, monoamine oxidases and β-amyloid aggregation inhibitory activities as potential agents against Alzheimer's disease.
Xu R, Xiao G, Li Y, Liu H, Song Q, Zhang X, Yang Z, Zheng Y, Tan Z, Deng Y.
Bioorg Med Chem (2018) 26 : 1885 -1895
PubMed 29500132 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 5.06 7.08

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL887 RASAGILINE 4.0 1 7.08
CHEMBL92401 IPRONIAZID 2.0 1 5.71
CHEMBL8706 CLORGILINE 2.0 1 5.38
CHEMBL4228361 1 4.91
CHEMBL4228401 1 4.88
CHEMBL4228676 1 4.86
CHEMBL4227568 1 4.73
CHEMBL4226833 1 4.72
CHEMBL4227620 1 4.71
CHEMBL4226245 1 4.71
CHEMBL4228589 1 4.71
CHEMBL4225991 1 4.70
CHEMBL4224820 1 4.70

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL887 RASAGILINE IC50 = 83.0 nM 7.08
CHEMBL92401 IPRONIAZID IC50 = 1950.0 nM 5.71
CHEMBL8706 CLORGILINE IC50 = 4190.0 nM 5.38
CHEMBL4228361 IC50 = 12400.0 nM 4.91
CHEMBL4228401 IC50 = 13200.0 nM 4.88
CHEMBL4228676 IC50 = 13700.0 nM 4.86
CHEMBL4227568 IC50 = 18800.0 nM 4.73
CHEMBL4226833 IC50 = 19200.0 nM 4.72
CHEMBL4227620 IC50 = 19700.0 nM 4.71
CHEMBL4226245 IC50 = 19400.0 nM 4.71
CHEMBL4228589 IC50 = 19600.0 nM 4.71
CHEMBL4225991 IC50 = 20100.0 nM 4.70
CHEMBL4224820 IC50 = 20100.0 nM 4.70