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Assay Detail

CHEMBL1216987

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

Binding
Inhibition of human HDAC6
15
Total Activities
15
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

Chemical phylogenetics of histone deacetylases.
Bradner JE, West N, Grachan ML, Greenberg EF, Haggarty SJ, Warnow T, Mazitschek R.
Nat Chem Biol (2010) 6 : 238 -243
PubMed 20139990 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 15 8.06 9.60

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL96051 SCRIPTAID 1 9.60
CHEMBL99 TRICHOSTATIN 1.0 1 9.00
CHEMBL483254 PANOBINOSTAT 4.0 1 8.82
CHEMBL408513 BELINOSTAT 4.0 1 8.80
CHEMBL98 VORINOSTAT 4.0 1 8.80
CHEMBL1213492 GIVINOSTAT 4.0 1 8.38
CHEMBL353581 PYROXAMIDE 1.0 1 8.32
CHEMBL343448 ROMIDEPSIN 4.0 1 8.02
CHEMBL356066 DACINOSTAT 2.0 1 8.02
CHEMBL320497 SUBEROHYDROXAMIC ACID 1 7.84
CHEMBL356769 TUBACIN 1 7.80
CHEMBL1213458 1 7.52
CHEMBL1213457 1 7.50
CHEMBL55895 PHENYLBUTYRYLHYDROXAMIC ACID 1 6.82
CHEMBL1213539 NILTUBACIN 1 5.66

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL96051 SCRIPTAID Ki = 0.25 nM 9.60
CHEMBL99 TRICHOSTATIN Ki = 1.0 nM 9.00
CHEMBL483254 PANOBINOSTAT Ki = 1.5 nM 8.82
CHEMBL408513 BELINOSTAT Ki = 1.6 nM 8.80
CHEMBL98 VORINOSTAT Ki = 1.6 nM 8.80
CHEMBL1213492 GIVINOSTAT Ki = 4.2 nM 8.38
CHEMBL353581 PYROXAMIDE Ki = 4.8 nM 8.32
CHEMBL343448 ROMIDEPSIN Ki = 9.5 nM 8.02
CHEMBL356066 DACINOSTAT Ki = 9.5 nM 8.02
CHEMBL320497 SUBEROHYDROXAMIC ACID Ki = 14.5 nM 7.84
CHEMBL356769 TUBACIN Ki = 16.0 nM 7.80
CHEMBL1213458 Ki = 30.0 nM 7.52
CHEMBL1213457 Ki = 32.0 nM 7.50
CHEMBL55895 PHENYLBUTYRYLHYDROXAMIC ACID Ki = 150.0 nM 6.82
CHEMBL1213539 NILTUBACIN Ki = 2200.0 nM 5.66