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Assay Detail

CHEMBL5628872

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

Binding
Inhibition of HDAC6 (unknown origin) using FTS as substrate preincubated for 10 mins followed by substrate addition measured after 1 min
2
Total Activities
2
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 6 (CHEMBL1865)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Tetrahydro-β-carboline derivatives as potent histone deacetylase 6 inhibitors with broad-spectrum antiproliferative activity.
Chen X, Wang J, Zhao P, Dang B, Liang T, Steimbach RR, Miller AK, Liu J, Wang X, Zhang T, Luan X, Hu J, Gao J.
Eur J Med Chem (2023) 260 : 115776 -115776
PubMed 37660484 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 8.46 8.59

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3693786 CITARINOSTAT 2.0 1 8.59
CHEMBL2364628 RICOLINOSTAT 2.0 1 8.33

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3693786 CITARINOSTAT IC50 = 2.6 nM 8.59
CHEMBL2364628 RICOLINOSTAT IC50 = 4.7 nM 8.33