Compile Data Set for Download or QSAR

Found 11 hits of ic50 for monomerid = 50341853   

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 3 (Homo sapiens (Human))	BDBM50341853 (2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...) Show SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1cccnc1)N=O Show InChI InChI=1S/C21H26N4O3/c1-22-21(27)19(25-28)11-4-2-3-5-12-20(26)24-18-10-6-8-16(14-18)17-9-7-13-23-15-17/h6-10,13-15,19H,2-5,11-12H2,1H3,(H,22,27)(H,24,26)	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	1.84E+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 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 9 (Homo sapiens (Human))	BDBM50341853 (2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...) Show SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1cccnc1)N=O Show InChI InChI=1S/C21H26N4O3/c1-22-21(27)19(25-28)11-4-2-3-5-12-20(26)24-18-10-6-8-16(14-18)17-9-7-13-23-15-17/h6-10,13-15,19H,2-5,11-12H2,1H3,(H,22,27)(H,24,26)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.21E+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 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 7 (Homo sapiens (Human))	BDBM50341853 (2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...) Show SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1cccnc1)N=O Show InChI InChI=1S/C21H26N4O3/c1-22-21(27)19(25-28)11-4-2-3-5-12-20(26)24-18-10-6-8-16(14-18)17-9-7-13-23-15-17/h6-10,13-15,19H,2-5,11-12H2,1H3,(H,22,27)(H,24,26)	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	4.28E+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 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))	BDBM50341853 (2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...) Show SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1cccnc1)N=O Show InChI InChI=1S/C21H26N4O3/c1-22-21(27)19(25-28)11-4-2-3-5-12-20(26)24-18-10-6-8-16(14-18)17-9-7-13-23-15-17/h6-10,13-15,19H,2-5,11-12H2,1H3,(H,22,27)(H,24,26)	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	7.67E+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 11 (Homo sapiens (Human))	BDBM50341853 (2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...) Show SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1cccnc1)N=O Show InChI InChI=1S/C21H26N4O3/c1-22-21(27)19(25-28)11-4-2-3-5-12-20(26)24-18-10-6-8-16(14-18)17-9-7-13-23-15-17/h6-10,13-15,19H,2-5,11-12H2,1H3,(H,22,27)(H,24,26)	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
Polyamine deacetylase HDAC10 (Homo sapiens (Human))	BDBM50341853 (2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...) Show SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1cccnc1)N=O Show InChI InChI=1S/C21H26N4O3/c1-22-21(27)19(25-28)11-4-2-3-5-12-20(26)24-18-10-6-8-16(14-18)17-9-7-13-23-15-17/h6-10,13-15,19H,2-5,11-12H2,1H3,(H,22,27)(H,24,26)	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
Histone deacetylase 4 (Homo sapiens (Human))	BDBM50341853 (2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...) Show SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1cccnc1)N=O Show InChI InChI=1S/C21H26N4O3/c1-22-21(27)19(25-28)11-4-2-3-5-12-20(26)24-18-10-6-8-16(14-18)17-9-7-13-23-15-17/h6-10,13-15,19H,2-5,11-12H2,1H3,(H,22,27)(H,24,26)	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
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50341853 (2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...) Show SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1cccnc1)N=O Show InChI InChI=1S/C21H26N4O3/c1-22-21(27)19(25-28)11-4-2-3-5-12-20(26)24-18-10-6-8-16(14-18)17-9-7-13-23-15-17/h6-10,13-15,19H,2-5,11-12H2,1H3,(H,22,27)(H,24,26)	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 1 (Homo sapiens (Human))	BDBM50341853 (2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...) Show SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1cccnc1)N=O Show InChI InChI=1S/C21H26N4O3/c1-22-21(27)19(25-28)11-4-2-3-5-12-20(26)24-18-10-6-8-16(14-18)17-9-7-13-23-15-17/h6-10,13-15,19H,2-5,11-12H2,1H3,(H,22,27)(H,24,26)	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 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 5 (Homo sapiens (Human))	BDBM50341853 (2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...) Show SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1cccnc1)N=O Show InChI InChI=1S/C21H26N4O3/c1-22-21(27)19(25-28)11-4-2-3-5-12-20(26)24-18-10-6-8-16(14-18)17-9-7-13-23-15-17/h6-10,13-15,19H,2-5,11-12H2,1H3,(H,22,27)(H,24,26)	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 6 (Homo sapiens (Human))	BDBM50341853 (2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...) Show SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1cccnc1)N=O Show InChI InChI=1S/C21H26N4O3/c1-22-21(27)19(25-28)11-4-2-3-5-12-20(26)24-18-10-6-8-16(14-18)17-9-7-13-23-15-17/h6-10,13-15,19H,2-5,11-12H2,1H3,(H,22,27)(H,24,26)	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 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