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Assay Detail

CHEMBL895226

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

Binding
Inhibition of rat brain mitochondria MAOA by radioenzymatic assay
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Subcellular Mitochondria
Confidence 9 — Direct single protein target
Curated By Intermediate

Target

Amine oxidase [flavin-containing] A (CHEMBL3358)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Solid-phase synthesis and insights into structure-activity relationships of safinamide analogues as potent and selective inhibitors of type B monoamine oxidase.
Leonetti F, Capaldi C, Pisani L, Nicolotti O, Muncipinto G, Stefanachi A, Cellamare S, Caccia C, Carotti A.
J Med Chem (2007) 50 : 4909 -4916
PubMed 17824599 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 4.41 5.07

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL348597 1 5.07
CHEMBL396267 1 4.91
CHEMBL231583 1 4.87
CHEMBL242409 1 4.67
CHEMBL243081 1 4.47
CHEMBL156994 1 4.43
CHEMBL82327 1 4.38
CHEMBL243512 1 4.35
CHEMBL243733 1 4.30
CHEMBL242835 1 4.14
CHEMBL394347 1 4.07
CHEMBL243058 1 4.05
CHEMBL244771 1 4.00
CHEMBL243059 1 4.00
CHEMBL352004 1 -
CHEMBL396778 SAFINAMIDE 4.0 1 -
CHEMBL242618 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL348597 IC50 = 8500.0 nM 5.07
CHEMBL396267 IC50 = 12400.0 nM 4.91
CHEMBL231583 IC50 = 13600.0 nM 4.87
CHEMBL242409 IC50 = 21200.0 nM 4.67
CHEMBL243081 IC50 = 34000.0 nM 4.47
CHEMBL156994 IC50 = 37000.0 nM 4.43
CHEMBL82327 IC50 = 42000.0 nM 4.38
CHEMBL243512 IC50 = 45000.0 nM 4.35
CHEMBL243733 IC50 = 50000.0 nM 4.30
CHEMBL242835 IC50 = 72000.0 nM 4.14
CHEMBL394347 IC50 = 84600.0 nM 4.07
CHEMBL243058 IC50 = 90000.0 nM 4.05
CHEMBL244771 IC50 = 100000.0 nM 4.00
CHEMBL243059 IC50 = 100000.0 nM 4.00
CHEMBL352004 IC50 = 101000.0 nM -
CHEMBL396778 SAFINAMIDE IC50 = 580000.0 nM -
CHEMBL242618 IC50 = 114000.0 nM -