Compile Data Set for Download or QSAR

Found 3 hits of ic50 for monomerid = 50047963   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Histone deacetylase 1 (Homo sapiens (Human))	BDBM50047963 (CHEMBL3314868) Show SMILES Nc1ccccc1NC(=O)c1ccc(cc1)-c1nnc(Cc2cccc3ccccc23)o1 Show InChI InChI=1S/C26H20N4O2/c27-22-10-3-4-11-23(22)28-25(31)18-12-14-19(15-13-18)26-30-29-24(32-26)16-20-8-5-7-17-6-1-2-9-21(17)20/h1-15H,16,27H2,(H,28,31)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	25
Sapienza University of Rome Curated by ChEMBL					Assay Description Inhibition of human recombinant HDAC1 using histone H3 substrate pre-incubated at room temperature for 15 mins before substrate addition by fluorimet...				J Med Chem 57: 6259-65 (2014) Article DOI: 10.1021/jm500303u BindingDB Entry DOI: 10.7270/Q2KK9DFZ
					More data for this Ligand-Target Pair
Histone deacetylase 6 (Homo sapiens (Human))	BDBM50047963 (CHEMBL3314868) Show SMILES Nc1ccccc1NC(=O)c1ccc(cc1)-c1nnc(Cc2cccc3ccccc23)o1 Show InChI InChI=1S/C26H20N4O2/c27-22-10-3-4-11-23(22)28-25(31)18-12-14-19(15-13-18)26-30-29-24(32-26)16-20-8-5-7-17-6-1-2-9-21(17)20/h1-15H,16,27H2,(H,28,31)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.61E+4	n/a	n/a	n/a	n/a	n/a	25
Sapienza University of Rome Curated by ChEMBL					Assay Description Inhibition of human recombinant HDAC6 pre-incubated at room temperature for 15 min before substrate addition by fluorimetric assay				J Med Chem 57: 6259-65 (2014) Article DOI: 10.1021/jm500303u BindingDB Entry DOI: 10.7270/Q2KK9DFZ
					More data for this Ligand-Target Pair
Histone deacetylase 4 (Homo sapiens (Human))	BDBM50047963 (CHEMBL3314868) Show SMILES Nc1ccccc1NC(=O)c1ccc(cc1)-c1nnc(Cc2cccc3ccccc23)o1 Show InChI InChI=1S/C26H20N4O2/c27-22-10-3-4-11-23(22)28-25(31)18-12-14-19(15-13-18)26-30-29-24(32-26)16-20-8-5-7-17-6-1-2-9-21(17)20/h1-15H,16,27H2,(H,28,31)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	25
Sapienza University of Rome Curated by ChEMBL					Assay Description Inhibition of human recombinant HDAC4 using non-histone trifluoroacetyl lysine substrate pre-incubated at room temperature for 15 mins before substra...				J Med Chem 57: 6259-65 (2014) Article DOI: 10.1021/jm500303u BindingDB Entry DOI: 10.7270/Q2KK9DFZ
					More data for this Ligand-Target Pair