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

CHEMBL924052

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

Binding
Inhibition of human HDAC6
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 Intermediate

Target

Histone deacetylase 6 (CHEMBL1865)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis, and evaluation of isoindolinone-hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors.
Lee S, Shinji C, Ogura K, Shimizu M, Maeda S, Sato M, Yoshida M, Hashimoto Y, Miyachi H.
Bioorg Med Chem Lett (2007) 17 : 4895 -4900
PubMed 17588744 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 6.24 7.28

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL99 TRICHOSTATIN 1.0 1 7.28
CHEMBL247217 1 6.64
CHEMBL247654 1 6.55
CHEMBL247653 1 6.12
CHEMBL247218 1 6.00
CHEMBL246199 1 4.82

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL99 TRICHOSTATIN IC50 = 53.0 nM 7.28
CHEMBL247217 IC50 = 230.0 nM 6.64
CHEMBL247654 IC50 = 280.0 nM 6.55
CHEMBL247653 IC50 = 750.0 nM 6.12
CHEMBL247218 IC50 = 990.0 nM 6.00
CHEMBL246199 IC50 = 15000.0 nM 4.82