BDBM50137826 8-Biphenyl-4-yl-8-oxo-octanoic acid (2-amino-phenyl)-amide::CHEMBL95213
SMILES: Nc1ccccc1NC(=O)CCCCCCC(=O)c1ccc(cc1)-c1ccccc1
InChI Key: InChIKey=GJRNLVQHVDGGNK-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50137826 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50137826
(8-Biphenyl-4-yl-8-oxo-octanoic acid (2-amino-pheny...)Show SMILES Nc1ccccc1NC(=O)CCCCCCC(=O)c1ccc(cc1)-c1ccccc1 Show InChI InChI=1S/C26H28N2O2/c27-23-12-8-9-13-24(23)28-26(30)15-7-2-1-6-14-25(29)22-18-16-21(17-19-22)20-10-4-3-5-11-20/h3-5,8-13,16-19H,1-2,6-7,14-15,27H2,(H,28,30) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | n/a | n/a | 1.00E+4 | n/a | n/a | n/a | n/a |
MethylGene Inc.
Curated by ChEMBL
| Assay Description Effect on induced hyperacetylation of histones in whole cells |
Bioorg Med Chem Lett 14: 283-7 (2003)
BindingDB Entry DOI: 10.7270/Q2BV7G17 |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50137826
(8-Biphenyl-4-yl-8-oxo-octanoic acid (2-amino-pheny...)Show SMILES Nc1ccccc1NC(=O)CCCCCCC(=O)c1ccc(cc1)-c1ccccc1 Show InChI InChI=1S/C26H28N2O2/c27-23-12-8-9-13-24(23)28-26(30)15-7-2-1-6-14-25(29)22-18-16-21(17-19-22)20-10-4-3-5-11-20/h3-5,8-13,16-19H,1-2,6-7,14-15,27H2,(H,28,30) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
MethylGene Inc.
Curated by ChEMBL
| Assay Description Ability to inhibit recombinant human histone deacetylase 1 (HDAC-1). |
Bioorg Med Chem Lett 14: 283-7 (2003)
BindingDB Entry DOI: 10.7270/Q2BV7G17 |
More data for this Ligand-Target Pair | |