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Assay Detail

CHEMBL5249366

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

Binding
Inhibition of human recombinant MAO-B assessed as inhibition of 4-hydroxyquinoline formation using kynuramine as substrate by fluorescence spectrophotometry analysis
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] B (CHEMBL2039)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

New β-arylchalcogeno amines with procognitive properties targeting Carbonic Anhydrases and Monoamine Oxidases.
Provensi G, Costa A, Rani B, Becagli MV, Vaiano F, Passani MB, Tanini D, Capperucci A, Carradori S, Petzer JP, Petzer A, Vullo D, Costantino G, Blandina P, Angeli A, Supuran CT.
Eur J Med Chem (2022) 244 : 114828 -114828
PubMed 36244185 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 4.67 5.55

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5281498 1 5.55
CHEMBL326294 ISATIN 1 5.41
CHEMBL5270139 1 4.87
CHEMBL5285077 1 4.78
CHEMBL5280535 1 4.67
CHEMBL5278584 1 4.44
CHEMBL5286143 1 4.43
CHEMBL1159896 1 4.24
CHEMBL5286089 1 4.19
CHEMBL5270106 1 4.08

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5281498 IC50 = 2790.0 nM 5.55
CHEMBL326294 ISATIN IC50 = 3900.0 nM 5.41
CHEMBL5270139 IC50 = 13400.0 nM 4.87
CHEMBL5285077 IC50 = 16700.0 nM 4.78
CHEMBL5280535 IC50 = 21300.0 nM 4.67
CHEMBL5278584 IC50 = 36500.0 nM 4.44
CHEMBL5286143 IC50 = 36800.0 nM 4.43
CHEMBL1159896 IC50 = 57300.0 nM 4.24
CHEMBL5286089 IC50 = 64800.0 nM 4.19
CHEMBL5270106 IC50 = 84200.0 nM 4.08