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Assay Detail

CHEMBL5738835

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Binding
Inhibitory Activity Assay: The inhibitory activity of the synthesized compounds above against EZH1 or EZH2 methyltransferase was measured. The experiments were consigned to Reaction Biology, and EZH1 or EZH2 activity was measured using a radiometric scintillation proximity assay. To measure the IC50 of the synthesized compounds for EZH1 or EZH2, 2.3 nmol/L EZH1 or EZH2, 1 μmol/L histone H3 (21-44)-lys(biotin), 1.5 μmol/L S-adenyl methionine (SAM), and 500 nmol/L 3H-SAM were added to the compounds or DMSO with a buffer solution and reacted for 90 minutes at room temperature. The buffer solution was comprised of 50 mmol/L Tris-HCl pH 8.0, 50 mmol/L NaCl, 1 mmol/L EDTA, 1 mmoL/L DTT, 1 mmol/L PMSF and 1% DMSO. Trichloroacetic acid was added to end the reaction, and SPA beads coated with PVT streptavidin were added followed by 1 hour reaction at room temperature. A TopCount NXT plate reader was used to measure the methylation value of the substrate peptide. The measured values were converted to percent activity, setting the mean value for wells treated with DMSO as 100% and the background mean value as 0%.
45
Total Activities
15
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Histone-lysine N-methyltransferase EZH2 (CHEMBL2189110)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Dioxoloisoquinolinone derivatives and use thereof
(2022)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 8.73 9.46
kon 15 - -
k_off 15 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5956024 3 9.46
CHEMBL6011932 3 9.44
CHEMBL5840996 3 9.23
CHEMBL5954404 3 8.92
CHEMBL6032817 3 8.92
CHEMBL4597193 VALEMETOSTAT 2.0 3 8.87
CHEMBL5882348 3 8.66
CHEMBL3414621 TAZEMETOSTAT 4.0 3 8.61
CHEMBL5922751 3 8.60
CHEMBL5960885 3 8.57
CHEMBL5791232 3 8.48
CHEMBL6012111 3 8.48
CHEMBL6022634 3 8.47
CHEMBL5982156 3 8.42
CHEMBL6057832 3 7.82

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5956024 IC50 = 0.35 nM 9.46
CHEMBL6011932 IC50 = 0.36 nM 9.44
CHEMBL5840996 IC50 = 0.59 nM 9.23
CHEMBL6032817 IC50 = 1.21 nM 8.92
CHEMBL5954404 IC50 = 1.2 nM 8.92
CHEMBL4597193 VALEMETOSTAT IC50 = 1.36 nM 8.87
CHEMBL5882348 IC50 = 2.2 nM 8.66
CHEMBL3414621 TAZEMETOSTAT IC50 = 2.45 nM 8.61
CHEMBL5922751 IC50 = 2.5 nM 8.60
CHEMBL5960885 IC50 = 2.7 nM 8.57
CHEMBL6012111 IC50 = 3.3 nM 8.48
CHEMBL5791232 IC50 = 3.3 nM 8.48
CHEMBL6022634 IC50 = 3.4 nM 8.47
CHEMBL5982156 IC50 = 3.8 nM 8.42
CHEMBL6057832 IC50 = 15.0 nM 7.82
CHEMBL6011932 k_off = - s-1 -
CHEMBL5954404 kon = - -
CHEMBL5954404 k_off = - s-1 -
CHEMBL6057832 kon = - -
CHEMBL6057832 k_off = - s-1 -
CHEMBL5956024 kon = - -
CHEMBL5956024 k_off = - s-1 -
CHEMBL5882348 k_off = - s-1 -
CHEMBL5840996 k_off = - s-1 -
CHEMBL6032817 kon = - -
CHEMBL6032817 k_off = - s-1 -
CHEMBL5922751 kon = - -
CHEMBL5922751 k_off = - s-1 -
CHEMBL6022634 k_off = - s-1 -
CHEMBL5882348 kon = - -
CHEMBL6011932 kon = - -
CHEMBL5840996 kon = - -
CHEMBL4597193 VALEMETOSTAT k_off = - s-1 -
CHEMBL4597193 VALEMETOSTAT kon = - -
CHEMBL3414621 TAZEMETOSTAT k_off = - s-1 -
CHEMBL3414621 TAZEMETOSTAT kon = - -
CHEMBL5960885 k_off = - s-1 -
CHEMBL5960885 kon = - -
CHEMBL6022634 kon = - -
CHEMBL5982156 kon = - -
CHEMBL6012111 k_off = - s-1 -
CHEMBL5982156 k_off = - s-1 -
CHEMBL6012111 kon = - -
CHEMBL5791232 kon = - -
CHEMBL5791232 k_off = - s-1 -