BDBM50138417 6-(Acetyl-hydroxy-amino)-hexanoic acid phenylamide::CHEMBL138293

SMILES: CC(=O)N(O)CCCCCC(=O)Nc1ccccc1

InChI Key: InChIKey=MQVQXHJIMHPFGC-UHFFFAOYSA-N

Data: 4 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50138417   

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
Cereblon/Histone deacetylase 6 (Homo sapiens (Human))	BDBM50138417 (6-(Acetyl-hydroxy-amino)-hexanoic acid phenylamide...) Show SMILES CC(=O)N(O)CCCCCC(=O)Nc1ccccc1 Show InChI InChI=1S/C14H20N2O3/c1-12(17)16(19)11-7-3-6-10-14(18)15-13-8-4-2-5-9-13/h2,4-5,8-9,19H,3,6-7,10-11H2,1H3,(H,15,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Inhibition of Histone deacetylase 6 (HDAC6) of HeLa nuclear extracts				Bioorg Med Chem Lett 14: 449-53 (2003) BindingDB Entry DOI: 10.7270/Q2HH6JH2
					More data for this Ligand-Target Pair
Histone deacetylase (Homo sapiens (Human))	BDBM50138417 (6-(Acetyl-hydroxy-amino)-hexanoic acid phenylamide...) Show SMILES CC(=O)N(O)CCCCCC(=O)Nc1ccccc1 Show InChI InChI=1S/C14H20N2O3/c1-12(17)16(19)11-7-3-6-10-14(18)15-13-8-4-2-5-9-13/h2,4-5,8-9,19H,3,6-7,10-11H2,1H3,(H,15,18)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Inhibition of Histone deacetylase (HDAC)of HeLa nuclear extracts				Bioorg Med Chem Lett 14: 449-53 (2003) BindingDB Entry DOI: 10.7270/Q2HH6JH2
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50138417 (6-(Acetyl-hydroxy-amino)-hexanoic acid phenylamide...) Show SMILES CC(=O)N(O)CCCCCC(=O)Nc1ccccc1 Show InChI InChI=1S/C14H20N2O3/c1-12(17)16(19)11-7-3-6-10-14(18)15-13-8-4-2-5-9-13/h2,4-5,8-9,19H,3,6-7,10-11H2,1H3,(H,15,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Inhibition of Histone deacetylase 2 (HDAC2) activity of HeLa nuclear extracts				Bioorg Med Chem Lett 14: 449-53 (2003) BindingDB Entry DOI: 10.7270/Q2HH6JH2
					More data for this Ligand-Target Pair
Histone deacetylase 8 (Homo sapiens (Human))	BDBM50138417 (6-(Acetyl-hydroxy-amino)-hexanoic acid phenylamide...) Show SMILES CC(=O)N(O)CCCCCC(=O)Nc1ccccc1 Show InChI InChI=1S/C14H20N2O3/c1-12(17)16(19)11-7-3-6-10-14(18)15-13-8-4-2-5-9-13/h2,4-5,8-9,19H,3,6-7,10-11H2,1H3,(H,15,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Inhibition of Histone deacetylase 8 (HDAC8) of HeLa nuclear extracts				Bioorg Med Chem Lett 14: 449-53 (2003) BindingDB Entry DOI: 10.7270/Q2HH6JH2
					More data for this Ligand-Target Pair