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Assay Detail

CHEMBL5127956

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Binding
Inhibition of N-terminal FLAG/His-tagged full-length human KDM5C (2 to 1560 residues) expressed in baculovirus infected Sf9 insect cells using peptide substrate incubated for 2 hrs by Alpha Screen assay
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type Sf9
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Lysine-specific demethylase 5C (CHEMBL2163176)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Drug discovery of histone lysine demethylases (KDMs) inhibitors (progress from 2018 to present).
He X, Zhang H, Zhang Y, Ye Y, Wang S, Bai R, Xie T, Ye XY.
Eur J Med Chem (2022) 231 : 114143 -114143
PubMed 35101649 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 8.06 8.06

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5199483 1 8.06

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5199483 IC50 = 8.8 nM 8.06