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Assay Detail

CHEMBL3707942

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Binding
Biological Assay: Human recombinant MAO A and MAO B were expressed in Pichia pastoris and purified as published (Binda C, et al., Proc. Natl. Acad. Sci. USA 100: 9750-9755, 2003) Inhibition assays and Ki values were measured using kynuramine (MAO A) and benzylamine (MAO B) as substrates at pH 7.5 according to published procedures (Binda C, et al., Proc. Natl. Acad. Sci. USA 100: 9750-9755, 2003). Mouse recombinant LSD2 was expressed in E. coli and purified as described (Karytinos A, et al., J. Biol. Chem. 284:17775-17782, 2009). Human recombinant LSD1/CoREST were expressed in E. coli as separate proteins and co-purified following previously reported procedures (Forneris F, et al. Trends Biochem Sci 33:181-189, 2008). Enzymatic activities and inhibition assays with both demethylases were carried out at pH 7.5-8.0 using a methylated H3 peptide (Forneris F, et al., J. Biol. Chem. 282: 20070-20074 2007, Karytinos A, et al., J. Biol. Chem. 284:17775-17782, 2009).
2
Total Activities
2
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

Tranylcypromine derivatives as inhibitors of histone demethylases LSD1 and/or LSD2
(2014)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 2 5.30 5.46

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1797640 1 5.46
CHEMBL1795981 1 5.13

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1797640 Ki = 3500.0 nM 5.46
CHEMBL1795981 Ki = 7400.0 nM 5.13