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Assay Detail

CHEMBL921442

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Binding
Inhibition of human HDAC1 expressed in 293T cells
6
Total Activities
6
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 Autocuration

Target

Histone deacetylase 1 (CHEMBL325)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Evaluation of antiangiogenic activity of azumamides by the in vitro vascular organization model using mouse induced pluripotent stem (iPS) cells.
Nakao Y, Narazaki G, Hoshino T, Maeda S, Yoshida M, Maejima H, Yamashita JK.
Bioorg Med Chem Lett (2008) 18 : 2982 -2984
PubMed 18397826 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 6.26 7.44

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL99 TRICHOSTATIN 1.0 1 7.44
CHEMBL257972 AZUMAMIDE C 1 5.93
CHEMBL402363 AZUMAMIDE E 1 5.91
CHEMBL402727 AZUMAMIDE B 1 5.74
CHEMBL255714 AZUMAMIDE A 1 -
CHEMBL257973 AZUMAMIDE D 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL99 TRICHOSTATIN IC50 = 36.6 nM 7.44
CHEMBL257972 AZUMAMIDE C IC50 = 1170.0 nM 5.93
CHEMBL402363 AZUMAMIDE E IC50 = 1220.0 nM 5.91
CHEMBL402727 AZUMAMIDE B IC50 = 1830.0 nM 5.74
CHEMBL255714 AZUMAMIDE A IC50 > 50000.0 nM -
CHEMBL257973 AZUMAMIDE D IC50 > 50000.0 nM -