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Assay Detail

CHEMBL5537996

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

Binding
Inhibition of human recombinant MAO-A using tyramine as substrate incubated for 20 mins by fluorometric assay
19
Total Activities
19
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

Discovery of C-3 isoxazole substituted thiochromone S,S-dioxide derivatives as potent and selective inhibitors for monoamine oxidase B (MAO-B).
Mi P, Tan Y, Ye S, Lang JJ, Lv Y, Jiang J, Chen L, Luo J, Lin Y, Yuan Z, Zheng X, Lin YW.
Eur J Med Chem (2024) 263 : 115956 -115956
PubMed 37992521 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 19 4.96 7.47

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL8706 CLORGILINE 2.0 1 7.47
CHEMBL5568907 1 4.67
CHEMBL5573057 1 4.42
CHEMBL5574276 1 4.19
CHEMBL5567290 1 4.07
CHEMBL5570452 1 -
CHEMBL5583701 1 -
CHEMBL5566383 1 -
CHEMBL5567284 1 -
CHEMBL5572200 1 -
CHEMBL5562510 1 -
CHEMBL5570896 1 -
CHEMBL5565806 1 -
CHEMBL5542744 1 -
CHEMBL5571892 1 -
CHEMBL5575276 1 -
CHEMBL1201142 RASAGILINE MESYLATE 4.0 1 -
CHEMBL396778 SAFINAMIDE 4.0 1 -
CHEMBL5590991 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL8706 CLORGILINE IC50 = 34.0 nM 7.47
CHEMBL5568907 IC50 = 21220.0 nM 4.67
CHEMBL5573057 IC50 = 38280.0 nM 4.42
CHEMBL5574276 IC50 = 64440.0 nM 4.19
CHEMBL5567290 IC50 = 85400.0 nM 4.07
CHEMBL5570452 IC50 = 160640.0 nM -
CHEMBL5583701 IC50 - -
CHEMBL5566383 IC50 - -
CHEMBL5567284 IC50 - -
CHEMBL5572200 IC50 - -
CHEMBL5562510 IC50 - -
CHEMBL5570896 IC50 - -
CHEMBL5565806 IC50 - -
CHEMBL5542744 IC50 - -
CHEMBL5571892 IC50 - -
CHEMBL5575276 IC50 - -
CHEMBL1201142 RASAGILINE MESYLATE IC50 - -
CHEMBL396778 SAFINAMIDE IC50 - -
CHEMBL5590991 IC50 - -