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Assay Detail

CHEMBL3591679

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

Binding
Inhibition of JHDM1F (unknown origin) using H3K9mel peptide
17
Total Activities
17
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

Histone lysine demethylase PHF8 (CHEMBL1938212)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Identification of Jumonji AT-Rich Interactive Domain 1A Inhibitors and Their Effect on Cancer Cells.
Itoh Y, Sawada H, Suzuki M, Tojo T, Sasaki R, Hasegawa M, Mizukami T, Suzuki T.
ACS Med Chem Lett (2015) 6 : 665 -670
PubMed 26101571 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 4.39 4.62

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3590431 1 4.62
CHEMBL3590430 1 4.54
CHEMBL3590421 1 4.24
CHEMBL3590427 1 4.14
CHEMBL3590418 1 -
CHEMBL3590419 1 -
CHEMBL3590420 1 -
CHEMBL3590422 1 -
CHEMBL3590423 1 -
CHEMBL3590424 1 -
CHEMBL90852 N-OXALYLGLYCINE 1 -
CHEMBL3590426 1 -
CHEMBL3590428 1 -
CHEMBL3590429 1 -
CHEMBL3590432 1 -
CHEMBL3590433 1 -
CHEMBL3590425 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3590431 IC50 = 24000.0 nM 4.62
CHEMBL3590430 IC50 = 29000.0 nM 4.54
CHEMBL3590421 IC50 = 58000.0 nM 4.24
CHEMBL3590427 IC50 = 73000.0 nM 4.14
CHEMBL3590418 IC50 > 100000.0 nM -
CHEMBL3590419 IC50 - -
CHEMBL3590420 IC50 - -
CHEMBL3590422 IC50 - -
CHEMBL3590423 IC50 - -
CHEMBL3590424 IC50 - -
CHEMBL90852 N-OXALYLGLYCINE IC50 = 640000.0 nM -
CHEMBL3590426 IC50 > 100000.0 nM -
CHEMBL3590428 IC50 - -
CHEMBL3590429 IC50 - -
CHEMBL3590432 IC50 - -
CHEMBL3590433 IC50 - -
CHEMBL3590425 IC50 - -