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Assay Detail

CHEMBL5156151

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

Binding
Inhibition of HDAC class 2a in human HT-29 cells using TFA-lysine as fluorogenic substrate by fluorescence microplate reader assay
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HT-29
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Design, synthesis, biochemical evaluation, radiolabeling and in vivo imaging with high affinity class-IIa histone deacetylase inhibitor for molecular imaging and targeted therapy.
Turkman N, Liu D, Pirola I.
Eur J Med Chem (2022) 228 : 114011 -114011
PubMed 34875522 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 6.00 6.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4751615 1 6.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4751615 IC50 = 1004.0 nM 6.00