Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL4828944

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

Binding
Inhibition of HDAC2 (unknown origin)
6
Total Activities
6
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 deacetylase 2 (CHEMBL1937)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of 2,4-pyrimidinediamine derivatives as potent dual inhibitors of ALK and HDAC.
Pan T, Dan Y, Guo D, Jiang J, Ran D, Zhang L, Tian B, Yuan J, Yu Y, Gan Z.
Eur J Med Chem (2021) 224 : 113672 -113672
PubMed 34237620 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 7.92 8.03

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4855319 1 8.03
CHEMBL98 VORINOSTAT 4.0 1 7.92
CHEMBL4849606 1 7.82
CHEMBL601719 CRIZOTINIB 4.0 1 -
CHEMBL2403108 CERITINIB 4.0 1 -
CHEMBL4298138 REPOTRECTINIB 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4855319 IC50 = 9.3 nM 8.03
CHEMBL98 VORINOSTAT IC50 = 12.0 nM 7.92
CHEMBL4849606 IC50 = 15.0 nM 7.82
CHEMBL601719 CRIZOTINIB IC50 - -
CHEMBL2403108 CERITINIB IC50 - -
CHEMBL4298138 REPOTRECTINIB IC50 - -