BDBM50341843 (S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N1-phenylnonanediamide::CHEMBL1767047

SMILES: CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O

InChI Key: InChIKey=WAZRMVAFNMGPBD-CPRJBALCSA-N

Data: 11 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 11 hits for monomerid = 50341843   

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 5 (Homo sapiens (Human))	BDBM50341843 ((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...) Show SMILES CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O |r| Show InChI InChI=1S/C30H36N4O3/c1-31-29(35)27(33-37)20-12-5-13-21-28(30(36)32-26-18-10-4-11-19-26)34(22-24-14-6-2-7-15-24)23-25-16-8-3-9-17-25/h2-4,6-11,14-19,27-28H,5,12-13,20-23H2,1H3,(H,31,35)(H,32,36)/t27?,28-/m0/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Siena Curated by ChEMBL					Assay Description Inhibition of human HDAC5 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assay				J Med Chem 54: 2165-82 (2011) Article DOI: 10.1021/jm101373a BindingDB Entry DOI: 10.7270/Q2CR5TNZ
					More data for this Ligand-Target Pair
Histone deacetylase 3 (Homo sapiens (Human))	BDBM50341843 ((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...) Show SMILES CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O |r| Show InChI InChI=1S/C30H36N4O3/c1-31-29(35)27(33-37)20-12-5-13-21-28(30(36)32-26-18-10-4-11-19-26)34(22-24-14-6-2-7-15-24)23-25-16-8-3-9-17-25/h2-4,6-11,14-19,27-28H,5,12-13,20-23H2,1H3,(H,31,35)(H,32,36)/t27?,28-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Siena Curated by ChEMBL					Assay Description Inhibition of human HDAC3 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assay				J Med Chem 54: 2165-82 (2011) Article DOI: 10.1021/jm101373a BindingDB Entry DOI: 10.7270/Q2CR5TNZ
					More data for this Ligand-Target Pair
Histone deacetylase 11 (Homo sapiens (Human))	BDBM50341843 ((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...) Show SMILES CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O |r| Show InChI InChI=1S/C30H36N4O3/c1-31-29(35)27(33-37)20-12-5-13-21-28(30(36)32-26-18-10-4-11-19-26)34(22-24-14-6-2-7-15-24)23-25-16-8-3-9-17-25/h2-4,6-11,14-19,27-28H,5,12-13,20-23H2,1H3,(H,31,35)(H,32,36)/t27?,28-/m0/s1	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Siena Curated by ChEMBL					Assay Description Inhibition of human HDAC11 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assay				J Med Chem 54: 2165-82 (2011) Article DOI: 10.1021/jm101373a BindingDB Entry DOI: 10.7270/Q2CR5TNZ
					More data for this Ligand-Target Pair
Histone deacetylase 1 (Homo sapiens (Human))	BDBM50341843 ((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...) Show SMILES CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O |r| Show InChI InChI=1S/C30H36N4O3/c1-31-29(35)27(33-37)20-12-5-13-21-28(30(36)32-26-18-10-4-11-19-26)34(22-24-14-6-2-7-15-24)23-25-16-8-3-9-17-25/h2-4,6-11,14-19,27-28H,5,12-13,20-23H2,1H3,(H,31,35)(H,32,36)/t27?,28-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Siena Curated by ChEMBL					Assay Description Inhibition of human HDAC1 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assay				J Med Chem 54: 2165-82 (2011) Article DOI: 10.1021/jm101373a BindingDB Entry DOI: 10.7270/Q2CR5TNZ
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50341843 ((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...) Show SMILES CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O |r| Show InChI InChI=1S/C30H36N4O3/c1-31-29(35)27(33-37)20-12-5-13-21-28(30(36)32-26-18-10-4-11-19-26)34(22-24-14-6-2-7-15-24)23-25-16-8-3-9-17-25/h2-4,6-11,14-19,27-28H,5,12-13,20-23H2,1H3,(H,31,35)(H,32,36)/t27?,28-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Siena Curated by ChEMBL					Assay Description Inhibition of human HDAC2 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assay				J Med Chem 54: 2165-82 (2011) Article DOI: 10.1021/jm101373a BindingDB Entry DOI: 10.7270/Q2CR5TNZ
					More data for this Ligand-Target Pair
Histone deacetylase 10 (Homo sapiens (Human))	BDBM50341843 ((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...) Show SMILES CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O |r| Show InChI InChI=1S/C30H36N4O3/c1-31-29(35)27(33-37)20-12-5-13-21-28(30(36)32-26-18-10-4-11-19-26)34(22-24-14-6-2-7-15-24)23-25-16-8-3-9-17-25/h2-4,6-11,14-19,27-28H,5,12-13,20-23H2,1H3,(H,31,35)(H,32,36)/t27?,28-/m0/s1	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Siena Curated by ChEMBL					Assay Description Inhibition of human HDAC10 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assay				J Med Chem 54: 2165-82 (2011) Article DOI: 10.1021/jm101373a BindingDB Entry DOI: 10.7270/Q2CR5TNZ
					More data for this Ligand-Target Pair
Cereblon/Histone deacetylase 6 (Homo sapiens (Human))	BDBM50341843 ((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...) Show SMILES CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O |r| Show InChI InChI=1S/C30H36N4O3/c1-31-29(35)27(33-37)20-12-5-13-21-28(30(36)32-26-18-10-4-11-19-26)34(22-24-14-6-2-7-15-24)23-25-16-8-3-9-17-25/h2-4,6-11,14-19,27-28H,5,12-13,20-23H2,1H3,(H,31,35)(H,32,36)/t27?,28-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.58E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Siena Curated by ChEMBL					Assay Description Inhibition of human HDAC6 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assay				J Med Chem 54: 2165-82 (2011) Article DOI: 10.1021/jm101373a BindingDB Entry DOI: 10.7270/Q2CR5TNZ
					More data for this Ligand-Target Pair
Histone deacetylase 7 (Homo sapiens (Human))	BDBM50341843 ((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...) Show SMILES CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O |r| Show InChI InChI=1S/C30H36N4O3/c1-31-29(35)27(33-37)20-12-5-13-21-28(30(36)32-26-18-10-4-11-19-26)34(22-24-14-6-2-7-15-24)23-25-16-8-3-9-17-25/h2-4,6-11,14-19,27-28H,5,12-13,20-23H2,1H3,(H,31,35)(H,32,36)/t27?,28-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Siena Curated by ChEMBL					Assay Description Inhibition of human HDAC7 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assay				J Med Chem 54: 2165-82 (2011) Article DOI: 10.1021/jm101373a BindingDB Entry DOI: 10.7270/Q2CR5TNZ
					More data for this Ligand-Target Pair
Histone deacetylase 8 (Homo sapiens (Human))	BDBM50341843 ((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...) Show SMILES CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O |r| Show InChI InChI=1S/C30H36N4O3/c1-31-29(35)27(33-37)20-12-5-13-21-28(30(36)32-26-18-10-4-11-19-26)34(22-24-14-6-2-7-15-24)23-25-16-8-3-9-17-25/h2-4,6-11,14-19,27-28H,5,12-13,20-23H2,1H3,(H,31,35)(H,32,36)/t27?,28-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Siena Curated by ChEMBL					Assay Description Inhibition of human HDAC8 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assay				J Med Chem 54: 2165-82 (2011) Article DOI: 10.1021/jm101373a BindingDB Entry DOI: 10.7270/Q2CR5TNZ
					More data for this Ligand-Target Pair
Histone deacetylase 9 (Homo sapiens (Human))	BDBM50341843 ((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...) Show SMILES CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O |r| Show InChI InChI=1S/C30H36N4O3/c1-31-29(35)27(33-37)20-12-5-13-21-28(30(36)32-26-18-10-4-11-19-26)34(22-24-14-6-2-7-15-24)23-25-16-8-3-9-17-25/h2-4,6-11,14-19,27-28H,5,12-13,20-23H2,1H3,(H,31,35)(H,32,36)/t27?,28-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Siena Curated by ChEMBL					Assay Description Inhibition of human HDAC9 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assay				J Med Chem 54: 2165-82 (2011) Article DOI: 10.1021/jm101373a BindingDB Entry DOI: 10.7270/Q2CR5TNZ
					More data for this Ligand-Target Pair
Histone deacetylase 4 (Homo sapiens (Human))	BDBM50341843 ((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...) Show SMILES CNC(=O)C(CCCCC[C@H](N(Cc1ccccc1)Cc1ccccc1)C(=O)Nc1ccccc1)N=O |r| Show InChI InChI=1S/C30H36N4O3/c1-31-29(35)27(33-37)20-12-5-13-21-28(30(36)32-26-18-10-4-11-19-26)34(22-24-14-6-2-7-15-24)23-25-16-8-3-9-17-25/h2-4,6-11,14-19,27-28H,5,12-13,20-23H2,1H3,(H,31,35)(H,32,36)/t27?,28-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universita` degli Studi di Siena Curated by ChEMBL					Assay Description Inhibition of human HDAC4 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assay				J Med Chem 54: 2165-82 (2011) Article DOI: 10.1021/jm101373a BindingDB Entry DOI: 10.7270/Q2CR5TNZ
					More data for this Ligand-Target Pair