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Assay Detail

CHEMBL1068958

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

Binding
Inhibition of human recombinant MAOA assessed as 4-hydroxyquinoline formation by fluorimetry
14
Total Activities
7
Compounds Tested
2
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

Inhibition of monoamine oxidase by 8-benzyloxycaffeine analogues.
Strydom B, Malan SF, Castagnoli N, Bergh JJ, Petzer JP.
Bioorg Med Chem (2010) 18 : 1018 -1028
PubMed 20093036 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 6.46 7.17
Ki 7 6.94 7.64

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL602464 2 7.64
CHEMBL602260 2 7.44
CHEMBL602466 2 7.29
CHEMBL602465 2 6.75
CHEMBL589765 2 6.75
CHEMBL602880 2 6.47
CHEMBL602259 2 6.23

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL602464 Ki = 23.0 nM 7.64
CHEMBL602260 Ki = 36.0 nM 7.44
CHEMBL602466 Ki = 51.0 nM 7.29
CHEMBL602464 IC50 = 68.0 nM 7.17
CHEMBL602260 IC50 = 107.0 nM 6.97
CHEMBL602466 IC50 = 152.0 nM 6.82
CHEMBL602465 Ki = 180.0 nM 6.75
CHEMBL589765 Ki = 180.0 nM 6.75
CHEMBL602880 Ki = 340.0 nM 6.47
CHEMBL602465 IC50 = 542.0 nM 6.27
CHEMBL589765 IC50 = 546.0 nM 6.26
CHEMBL602259 Ki = 590.0 nM 6.23
CHEMBL602880 IC50 = 1010.0 nM 6.00
CHEMBL602259 IC50 = 1770.0 nM 5.75