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Assay Detail

CHEMBL5217064

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

Binding
Inhibition of HDAC11 (unknown origin) measured by fluorescence based assay
4
Total Activities
4
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 11 (CHEMBL3310)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Identification of PI3K/HDAC Dual-targeted inhibitors with subtype selectivity as potential therapeutic agents against solid Tumors: Building HDAC6 potency in a Quinazolinone-based PI3Kδ-selective template.
Li Z, Zhao C, He G, Wang Y, Wang Y, Ma X.
Bioorg Med Chem (2022) 73 : 117028 -117028
PubMed 36182802 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 5.81 5.81

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5218472 1 5.81
CHEMBL98 VORINOSTAT 4.0 1 -
CHEMBL2364628 RICOLINOSTAT 2.0 1 -
CHEMBL2018302 TUBASTATIN A 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5218472 IC50 = 1547.0 nM 5.81
CHEMBL98 VORINOSTAT IC50 > 5000.0 nM -
CHEMBL2364628 RICOLINOSTAT IC50 > 5000.0 nM -
CHEMBL2018302 TUBASTATIN A IC50 > 5000.0 nM -