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Assay Detail

CHEMBL5540464

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

Binding
Inhibition of LSD1 (unknown origin)
7
Total Activities
7
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

Combination Therapy and Dual-Target Inhibitors Based on LSD1: New Emerging Tools in Cancer Therapy.
Shen L, Wang B, Wang SP, Ji SK, Fu MJ, Wang SW, Hou WQ, Dai XJ, Liu HM.
J Med Chem (2024) 67 : 922 -951
PubMed 38214982 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 6.92 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5029010 1 8.40
CHEMBL3104250 1 7.89
CHEMBL4301645 1 7.80
CHEMBL3781751 IADADEMSTAT 2.0 1 7.75
CHEMBL3786182 GSK2879552 1.0 1 7.62
CHEMBL3989843 TRANYLCYPROMINE 4.0 1 4.68
CHEMBL2426136 NAMOLINE 1 4.29

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5029010 IC50 = 4.0 nM 8.40
CHEMBL3104250 IC50 = 13.0 nM 7.89
CHEMBL4301645 IC50 = 16.0 nM 7.80
CHEMBL3781751 IADADEMSTAT IC50 = 18.0 nM 7.75
CHEMBL3786182 GSK2879552 IC50 = 24.0 nM 7.62
CHEMBL3989843 TRANYLCYPROMINE IC50 = 20700.0 nM 4.68
CHEMBL2426136 NAMOLINE IC50 = 51000.0 nM 4.29