null

SMILES: ONC(=O)c1ccc(NC2CCN(C2)c2ccc(Cl)cc2)cc1

InChI Key: InChIKey=WEZUWBUJRJCUNX-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50078692   

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 1 (Homo sapiens (Human))	BDBM50078692 (CHEMBL3415625) Show SMILES ONC(=O)c1ccc(NC2CCN(C2)c2ccc(Cl)cc2)cc1 Show InChI InChI=1S/C17H18ClN3O2/c18-13-3-7-16(8-4-13)21-10-9-15(11-21)19-14-5-1-12(2-6-14)17(22)20-23/h1-8,15,19,23H,9-11H2,(H,20,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.92E+4	n/a	n/a	n/a	n/a	n/a	n/a
Roche Innovation Center Shanghai Curated by ChEMBL					Assay Description Inhibition of HDAC1 (unknown origin) using RHKK(Ac)AMC as substrate				J Med Chem 58: 2809-20 (2015) Article DOI: 10.1021/jm502011f BindingDB Entry DOI: 10.7270/Q2B56MF0
					More data for this Ligand-Target Pair
Histone deacetylase 8 (Homo sapiens (Human))	BDBM50078692 (CHEMBL3415625) Show SMILES ONC(=O)c1ccc(NC2CCN(C2)c2ccc(Cl)cc2)cc1 Show InChI InChI=1S/C17H18ClN3O2/c18-13-3-7-16(8-4-13)21-10-9-15(11-21)19-14-5-1-12(2-6-14)17(22)20-23/h1-8,15,19,23H,9-11H2,(H,20,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	860	n/a	n/a	n/a	n/a	n/a	n/a
Roche Innovation Center Shanghai Curated by ChEMBL					Assay Description Inhibition of HDAC8 (unknown origin) using RHK(Ac)K(Ac)AMC as substrate				J Med Chem 58: 2809-20 (2015) Article DOI: 10.1021/jm502011f BindingDB Entry DOI: 10.7270/Q2B56MF0
					More data for this Ligand-Target Pair
Histone deacetylase 6 (Homo sapiens (Human))	BDBM50078692 (CHEMBL3415625) Show SMILES ONC(=O)c1ccc(NC2CCN(C2)c2ccc(Cl)cc2)cc1 Show InChI InChI=1S/C17H18ClN3O2/c18-13-3-7-16(8-4-13)21-10-9-15(11-21)19-14-5-1-12(2-6-14)17(22)20-23/h1-8,15,19,23H,9-11H2,(H,20,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	4.30E+3	n/a	n/a	n/a	n/a
Roche Innovation Center Shanghai Curated by ChEMBL					Assay Description Inhibition of HDAC6 in human A549 cells assessed as induction of tubulin acetylation after 17 to 18 hrs by ELISA				J Med Chem 58: 2809-20 (2015) Article DOI: 10.1021/jm502011f BindingDB Entry DOI: 10.7270/Q2B56MF0
					More data for this Ligand-Target Pair
Histone deacetylase 6 (Homo sapiens (Human))	BDBM50078692 (CHEMBL3415625) Show SMILES ONC(=O)c1ccc(NC2CCN(C2)c2ccc(Cl)cc2)cc1 Show InChI InChI=1S/C17H18ClN3O2/c18-13-3-7-16(8-4-13)21-10-9-15(11-21)19-14-5-1-12(2-6-14)17(22)20-23/h1-8,15,19,23H,9-11H2,(H,20,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	860	n/a	n/a	n/a	n/a	n/a	n/a
Roche Innovation Center Shanghai Curated by ChEMBL					Assay Description Inhibition of HDAC6 (unknown origin) using RHKK(Ac)AMC as substrate				J Med Chem 58: 2809-20 (2015) Article DOI: 10.1021/jm502011f BindingDB Entry DOI: 10.7270/Q2B56MF0
					More data for this Ligand-Target Pair