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Assay Detail

CHEMBL4370404

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

Binding
Inhibition of recombinant human HDAC6 using RHKKAc fluorogenic peptide substrate
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

Synthesis and Biological Investigation of Phenothiazine-Based Benzhydroxamic Acids as Selective Histone Deacetylase 6 Inhibitors.
Vögerl K, Ong N, Senger J, Herp D, Schmidtkunz K, Marek M, Müller M, Bartel K, Shaik TB, Porter NJ, Robaa D, Christianson DW, Romier C, Sippl W, Jung M, Bracher F.
J Med Chem (2019) 62 : 1138 -1166
PubMed 30645113 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 8.11 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL356769 TUBACIN 1 8.40
CHEMBL2018302 TUBASTATIN A 1 7.82

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL356769 TUBACIN IC50 = 4.0 nM 8.40
CHEMBL2018302 TUBASTATIN A IC50 = 15.0 nM 7.82