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Assay Detail

CHEMBL5159747

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

Binding
Inhibition of human LSD1 using H3K4Me2 peptide as substrate incubated for 60 min by horseradish peroxidase coupled assay
1
Total Activities
1
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

Lysine-specific histone demethylase 1A (CHEMBL6136)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-Activity Relationship Study of Indolin-5-yl-cyclopropanamine Derivatives as Selective Lysine Specific Demethylase 1 (LSD1) Inhibitors.
Li C, Su M, Zhu W, Kan W, Ge T, Xu G, Wang S, Sheng L, Gao F, Ye Y, Wang J, Zhou Y, Li J, Liu H.
J Med Chem (2022) 65 : 4335 -4349
PubMed 35200034 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 6.80 6.80

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3786182 GSK2879552 1.0 1 6.80

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3786182 GSK2879552 IC50 = 160.0 nM 6.80