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Assay Detail

CHEMBL5144883

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

Binding
Inhibition of recombinant human MAO-B expressed in baculovirus infected BTI insect cells using kynuramine as substrate after 20 mins by fluorescence spectrophotometric assay
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type BTI
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Amine oxidase [flavin-containing] B (CHEMBL2039)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Phenothiazine, anthraquinone and related tricyclic derivatives as inhibitors of monoamine oxidase.
Lefin R, Petzer A, Petzer JP.
Bioorg Med Chem (2022) 54 : 116558 -116558
PubMed 34915314 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 4.86 5.87

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5201468 1 5.87
CHEMBL89626 1 5.62
CHEMBL289277 EMODIN 1 5.49
CHEMBL179617 1 5.37
CHEMBL298398 ANTHRAFLAVICACID 1 5.25
CHEMBL486760 XANTHENE 1 5.13
CHEMBL40275 ALOE-EMODIN 1 4.66
CHEMBL294264 PURPURIN 1 4.40
CHEMBL53418 DANTHRON 4.0 1 4.23
CHEMBL2322655 CINNABARINIC ACID 1 4.19
CHEMBL2180144 1 4.04
CHEMBL5204890 1 4.04
CHEMBL43184 AMINACRINE 2.0 1 -
CHEMBL17594 QUINIZARIN 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5201468 IC50 = 1340.0 nM 5.87
CHEMBL89626 IC50 = 2410.0 nM 5.62
CHEMBL289277 EMODIN IC50 = 3240.0 nM 5.49
CHEMBL179617 IC50 = 4280.0 nM 5.37
CHEMBL298398 ANTHRAFLAVICACID IC50 = 5620.0 nM 5.25
CHEMBL486760 XANTHENE IC50 = 7420.0 nM 5.13
CHEMBL40275 ALOE-EMODIN IC50 = 21900.0 nM 4.66
CHEMBL294264 PURPURIN IC50 = 40200.0 nM 4.40
CHEMBL53418 DANTHRON IC50 = 58700.0 nM 4.23
CHEMBL2322655 CINNABARINIC ACID IC50 = 65000.0 nM 4.19
CHEMBL2180144 IC50 = 91900.0 nM 4.04
CHEMBL5204890 IC50 = 92000.0 nM 4.04
CHEMBL43184 AMINACRINE IC50 = 112000.0 nM -
CHEMBL17594 QUINIZARIN IC50 = 110000.0 nM -