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Assay Detail

CHEMBL925325

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Binding
Inhibition of human HDAC4 expressed in 293T cells
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type 293T
Confidence 9 — Direct single protein target
Curated By Intermediate

Target

Histone deacetylase 4 (CHEMBL3524)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Molecular design of histone deacetylase inhibitors by aromatic ring shifting in chlamydocin framework.
Shivashimpi GM, Amagai S, Kato T, Nishino N, Maeda S, Nishino TG, Yoshida M.
Bioorg Med Chem (2007) 15 : 7830 -7839
PubMed 17881232 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 8.32 8.80

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL241555 1 8.80
CHEMBL394261 1 8.80
CHEMBL238829 1 8.74
CHEMBL99 TRICHOSTATIN 1.0 1 8.70
CHEMBL393464 1 8.66
CHEMBL390991 1 8.62
CHEMBL391384 1 8.57
CHEMBL391383 1 8.49
CHEMBL393961 1 8.40
CHEMBL238587 1 8.38
CHEMBL238596 1 8.28
CHEMBL393260 1 7.60
CHEMBL428737 1 7.25
CHEMBL393261 1 7.16

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL241555 IC50 = 1.6 nM 8.80
CHEMBL394261 IC50 = 1.6 nM 8.80
CHEMBL238829 IC50 = 1.8 nM 8.74
CHEMBL99 TRICHOSTATIN IC50 = 2.0 nM 8.70
CHEMBL393464 IC50 = 2.2 nM 8.66
CHEMBL390991 IC50 = 2.4 nM 8.62
CHEMBL391384 IC50 = 2.7 nM 8.57
CHEMBL391383 IC50 = 3.2 nM 8.49
CHEMBL393961 IC50 = 4.0 nM 8.40
CHEMBL238587 IC50 = 4.2 nM 8.38
CHEMBL238596 IC50 = 5.2 nM 8.28
CHEMBL393260 IC50 = 25.0 nM 7.60
CHEMBL428737 IC50 = 56.0 nM 7.25
CHEMBL393261 IC50 = 70.0 nM 7.16