BDBM50263481 CHEMBL4074800

SMILES: CN1CN2CC(c3c(C2)n(Cc2ccc(cc2)C(=O)NO)c2ccccc32)C1=O

InChI Key: InChIKey=ZNIMBGDYTMHQRA-UHFFFAOYSA-N

Data: 3 KI

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 3 hits for monomerid = 50263481   

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))	BDBM50263481 (CHEMBL4074800) Show SMILES CN1CN2CC(c3c(C2)n(Cc2ccc(cc2)C(=O)NO)c2ccccc32)C1=O Show InChI InChI=1S/C22H22N4O3/c1-24-13-25-11-17(22(24)28)20-16-4-2-3-5-18(16)26(19(20)12-25)10-14-6-8-15(9-7-14)21(27)23-29/h2-9,17,29H,10-13H2,1H3,(H,23,27)	PDB MMDB NCI pathway Reactome pathway KEGG B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	0.230	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Pharmacy, Faculty of Chemistry and Pharmacy , University of Regensburg , 93040 Regensburg , Germany. Curated by ChEMBL					Assay Description Inhibition of full length recombinant human N-terminal GST-tagged HDAC6 expressed in baculovirus-infected Sf9 insect cells using RHKK(Ac)AMC as subst...				J Med Chem 61: 3454-3477 (2018) Article DOI: 10.1021/acs.jmedchem.7b01593 BindingDB Entry DOI: 10.7270/Q24B33S0
					More data for this Ligand-Target Pair
Histone deacetylase 8 (Homo sapiens (Human))	BDBM50263481 (CHEMBL4074800) Show SMILES CN1CN2CC(c3c(C2)n(Cc2ccc(cc2)C(=O)NO)c2ccccc32)C1=O Show InChI InChI=1S/C22H22N4O3/c1-24-13-25-11-17(22(24)28)20-16-4-2-3-5-18(16)26(19(20)12-25)10-14-6-8-15(9-7-14)21(27)23-29/h2-9,17,29H,10-13H2,1H3,(H,23,27)	PDB MMDB NCI pathway Reactome pathway KEGG B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	427	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Pharmacy, Faculty of Chemistry and Pharmacy , University of Regensburg , 93040 Regensburg , Germany. Curated by ChEMBL					Assay Description Inhibition of recombinant human C-terminal His-tagged HDAC8 (1 to 377 residues) expressed in baculovirus-infected insect cells using RHK(Ac)K(Ac)AMC ...				J Med Chem 61: 3454-3477 (2018) Article DOI: 10.1021/acs.jmedchem.7b01593 BindingDB Entry DOI: 10.7270/Q24B33S0
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50263481 (CHEMBL4074800) Show SMILES CN1CN2CC(c3c(C2)n(Cc2ccc(cc2)C(=O)NO)c2ccccc32)C1=O Show InChI InChI=1S/C22H22N4O3/c1-24-13-25-11-17(22(24)28)20-16-4-2-3-5-18(16)26(19(20)12-25)10-14-6-8-15(9-7-14)21(27)23-29/h2-9,17,29H,10-13H2,1H3,(H,23,27)	PDB MMDB NCI pathway Reactome pathway KEGG B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	1.36E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Pharmacy, Faculty of Chemistry and Pharmacy , University of Regensburg , 93040 Regensburg , Germany. Curated by ChEMBL					Assay Description Inhibition of full length recombinant human C-terminal GST-tagged HDAC2 expressed in baculovirus-infected insect cells using RHKK(Ac)AMC as substrate...				J Med Chem 61: 3454-3477 (2018) Article DOI: 10.1021/acs.jmedchem.7b01593 BindingDB Entry DOI: 10.7270/Q24B33S0
					More data for this Ligand-Target Pair