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Assay Detail

CHEMBL5537731

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

Binding
Inhibition of HDAC11 (unknown origin)
5
Total Activities
5
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

5-(Trifluoromethyl)-1,2,4-oxadiazole (TFMO)-based highly selective class IIa HDAC inhibitors exhibit synergistic anticancer activity in combination with bortezomib.
Asfaha Y, Bollmann LM, Skerhut AJ, Fischer F, Horstick N, Roth D, Wecker M, Mammen C, Smits SHJ, Fluegen G, Kassack MU, Kurz T.
Eur J Med Chem (2024) 263 : 115907 -115907
PubMed 37979441 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 4.18 4.18

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3692688 1 4.18
CHEMBL5563683 1 -
CHEMBL5572470 1 -
CHEMBL5571546 1 -
CHEMBL5575926 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3692688 IC50 = 66000.0 nM 4.18
CHEMBL5563683 IC50 > 100000.0 nM -
CHEMBL5572470 IC50 > 100000.0 nM -
CHEMBL5571546 IC50 > 100000.0 nM -
CHEMBL5575926 IC50 > 100000.0 nM -