Compile Data Set for Download or QSAR

Found 53 hits with Last Name = 'frick' and Initial = 'dn'   

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))	BDBM50048864 (CHEMBL3310505) Show SMILES [H][C@@]12CC(=O)N[C@H](C(C)C)C(=O)N[C@]([H])(CSSCC\C=C\1)C(=O)N\C(=C/C)C(=O)N[C@@H](C(C)C)C(=O)O2 |r,t:20| Show InChI InChI=1S/C24H36N4O6S2/c1-6-16-21(30)28-20(14(4)5)24(33)34-15-9-7-8-10-35-36-12-17(22(31)25-16)26-23(32)19(13(2)3)27-18(29)11-15/h6-7,9,13-15,17,19-20H,8,10-12H2,1-5H3,(H,25,31)(H,26,32)(H,27,29)(H,28,30)/b9-7+,16-6-/t15-,17+,19+,20-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of HDAC3 in human DU-145 cells assessed as increase in histone H3 acetylation after 24 hrs by immunofluorescence microscopy				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 1 (Homo sapiens (Human))	BDBM50048864 (CHEMBL3310505) Show SMILES [H][C@@]12CC(=O)N[C@H](C(C)C)C(=O)N[C@]([H])(CSSCC\C=C\1)C(=O)N\C(=C/C)C(=O)N[C@@H](C(C)C)C(=O)O2 |r,t:20| Show InChI InChI=1S/C24H36N4O6S2/c1-6-16-21(30)28-20(14(4)5)24(33)34-15-9-7-8-10-35-36-12-17(22(31)25-16)26-23(32)19(13(2)3)27-18(29)11-15/h6-7,9,13-15,17,19-20H,8,10-12H2,1-5H3,(H,25,31)(H,26,32)(H,27,29)(H,28,30)/b9-7+,16-6-/t15-,17+,19+,20-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.40	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of HDAC1 in human DU-145 cells assessed as increase in histone H3 acetylation after 24 hrs by immunofluorescence microscopy				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50048864 (CHEMBL3310505) Show SMILES [H][C@@]12CC(=O)N[C@H](C(C)C)C(=O)N[C@]([H])(CSSCC\C=C\1)C(=O)N\C(=C/C)C(=O)N[C@@H](C(C)C)C(=O)O2 |r,t:20| Show InChI InChI=1S/C24H36N4O6S2/c1-6-16-21(30)28-20(14(4)5)24(33)34-15-9-7-8-10-35-36-12-17(22(31)25-16)26-23(32)19(13(2)3)27-18(29)11-15/h6-7,9,13-15,17,19-20H,8,10-12H2,1-5H3,(H,25,31)(H,26,32)(H,27,29)(H,28,30)/b9-7+,16-6-/t15-,17+,19+,20-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.70	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of HDAC2 in human DU-145 cells assessed as increase in histone H3 acetylation after 24 hrs by immunofluorescence microscopy				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 8 (Homo sapiens (Human))	BDBM50048864 (CHEMBL3310505) Show SMILES [H][C@@]12CC(=O)N[C@H](C(C)C)C(=O)N[C@]([H])(CSSCC\C=C\1)C(=O)N\C(=C/C)C(=O)N[C@@H](C(C)C)C(=O)O2 |r,t:20| Show InChI InChI=1S/C24H36N4O6S2/c1-6-16-21(30)28-20(14(4)5)24(33)34-15-9-7-8-10-35-36-12-17(22(31)25-16)26-23(32)19(13(2)3)27-18(29)11-15/h6-7,9,13-15,17,19-20H,8,10-12H2,1-5H3,(H,25,31)(H,26,32)(H,27,29)(H,28,30)/b9-7+,16-6-/t15-,17+,19+,20-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of HDAC8 in human DU-145 cells assessed as increase in histone H3 acetylation after 24 hrs by immunofluorescence microscopy				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 6 (Homo sapiens (Human))	BDBM50048864 (CHEMBL3310505) Show SMILES [H][C@@]12CC(=O)N[C@H](C(C)C)C(=O)N[C@]([H])(CSSCC\C=C\1)C(=O)N\C(=C/C)C(=O)N[C@@H](C(C)C)C(=O)O2 |r,t:20| Show InChI InChI=1S/C24H36N4O6S2/c1-6-16-21(30)28-20(14(4)5)24(33)34-15-9-7-8-10-35-36-12-17(22(31)25-16)26-23(32)19(13(2)3)27-18(29)11-15/h6-7,9,13-15,17,19-20H,8,10-12H2,1-5H3,(H,25,31)(H,26,32)(H,27,29)(H,28,30)/b9-7+,16-6-/t15-,17+,19+,20-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of HDAC6 in human DU-145 cells assessed as increase in histone H3 acetylation after 24 hrs by immunofluorescence microscopy				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61947 (6-bromanyl-2-phenyl-1,2-benzothiazol-3-one | 6-bro...) Show SMILES Brc1ccc2c(c1)sn(-c1ccccc1)c2=O Show InChI InChI=1S/C13H8BrNOS/c14-9-6-7-11-12(8-9)17-15(13(11)16)10-4-2-1-3-5-10/h1-8H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	700	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM34233 (2-Phenyl-benzo[d]isoselenazol-3-one | 2-Phenyl-ben...) Show SMILES O=c1n([se]c2ccccc12)-c1ccccc1 Show InChI InChI=1S/C13H9NOSe/c15-13-11-8-4-5-9-12(11)16-14(13)10-6-2-1-3-7-10/h1-9H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61939 (5,6-bis(fluoranyl)-2-phenyl-1,2-benzothiazol-3-one...) Show SMILES Fc1cc2sn(-c3ccccc3)c(=O)c2cc1F Show InChI InChI=1S/C13H7F2NOS/c14-10-6-9-12(7-11(10)15)18-16(13(9)17)8-4-2-1-3-5-8/h1-7H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM46667 (2-phenyl-1,2-benzothiazol-3-one | 2-phenyl-1,2-ben...) Show SMILES O=c1n(sc2ccccc12)-c1ccccc1 Show InChI InChI=1S/C13H9NOS/c15-13-11-8-4-5-9-12(11)16-14(13)10-6-2-1-3-7-10/h1-9H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61966 (KSC-09-149B | KUC105615N | N-(2-chlorophenyl)-2-(3...) Show SMILES Clc1ccccc1NC(=O)Cn1sc2ccccc2c1=O Show InChI InChI=1S/C15H11ClN2O2S/c16-11-6-2-3-7-12(11)17-14(19)9-18-15(20)10-5-1-4-8-13(10)21-18/h1-8H,9H2,(H,17,19)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61969 (KSC-09-140B | KUC105618N | N-(2-bromophenyl)-2-(3-...) Show SMILES Brc1ccccc1NC(=O)Cn1sc2ccccc2c1=O Show InChI InChI=1S/C15H11BrN2O2S/c16-11-6-2-3-7-12(11)17-14(19)9-18-15(20)10-5-1-4-8-13(10)21-18/h1-8H,9H2,(H,17,19)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61942 (2-(3-keto-1,2-benzothiazol-2-yl)-N-(o-tolyl)acetam...) Show SMILES Cc1ccccc1NC(=O)Cn1sc2ccccc2c1=O Show InChI InChI=1S/C16H14N2O2S/c1-11-6-2-4-8-13(11)17-15(19)10-18-16(20)12-7-3-5-9-14(12)21-18/h2-9H,10H2,1H3,(H,17,19)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.90E+3	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61965 (KSC-09-149A | KUC105614N | N-(2-fluorophenyl)-2-(3...) Show SMILES Fc1ccccc1NC(=O)Cn1sc2ccccc2c1=O Show InChI InChI=1S/C15H11FN2O2S/c16-11-6-2-3-7-12(11)17-14(19)9-18-15(20)10-5-1-4-8-13(10)21-18/h1-8H,9H2,(H,17,19)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.60E+3	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61942 (2-(3-keto-1,2-benzothiazol-2-yl)-N-(o-tolyl)acetam...) Show SMILES Cc1ccccc1NC(=O)Cn1sc2ccccc2c1=O Show InChI InChI=1S/C16H14N2O2S/c1-11-6-2-4-8-13(11)17-15(19)10-18-16(20)12-7-3-5-9-14(12)21-18/h2-9H,10H2,1H3,(H,17,19)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.60E+3	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61964 (2-(3-keto-1,2-benzothiazol-2-yl)-N-phenyl-propiona...) Show SMILES CC(C(=O)Nc1ccccc1)n1sc2ccccc2c1=O Show InChI InChI=1S/C16H14N2O2S/c1-11(15(19)17-12-7-3-2-4-8-12)18-16(20)13-9-5-6-10-14(13)21-18/h2-11H,1H3,(H,17,19)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.30E+3	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61970 (KSC-09-140C | KUC105619N | N-(2-iodanylphenyl)-2-(...) Show SMILES Ic1ccccc1NC(=O)Cn1sc2ccccc2c1=O Show InChI InChI=1S/C15H11IN2O2S/c16-11-6-2-3-7-12(11)17-14(19)9-18-15(20)10-5-1-4-8-13(10)21-18/h1-8H,9H2,(H,17,19)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.80E+3	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Histone deacetylase 3 (Homo sapiens (Human))	BDBM50585748 (CHEMBL5086240) Show SMILES CC(C)(C)OC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)OC(C)(C)C Show InChI	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of HDAC3 in human DU-145 cells assessed as increase in histone H3 acetylation after 24 hrs by immunofluorescence microscopy				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 1 (Homo sapiens (Human))	BDBM50585748 (CHEMBL5086240) Show SMILES CC(C)(C)OC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)OC(C)(C)C Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of HDAC1 in human DU-145 cells assessed as increase in histone H3 acetylation after 24 hrs by immunofluorescence microscopy				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585748 (CHEMBL5086240) Show SMILES CC(C)(C)OC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)OC(C)(C)C Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of HDAC2 in human DU-145 cells assessed as increase in histone H3 acetylation after 24 hrs by immunofluorescence microscopy				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585748 (CHEMBL5086240) Show SMILES CC(C)(C)OC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)OC(C)(C)C Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 preincubated for 20 mins with DTT followed by enzyme addition and measured after 10 mins by Glo-lum...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 8 (Homo sapiens (Human))	BDBM50585748 (CHEMBL5086240) Show SMILES CC(C)(C)OC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)OC(C)(C)C Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of HDAC8 in human DU-145 cells assessed as increase in histone H3 acetylation after 24 hrs by immunofluorescence microscopy				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585743 (CHEMBL5087342) Show SMILES CCCC[C@@H](NC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)N[C@H](CCCC)C(O)=O)C(O)=O |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 preincubated for 20 mins with DTT followed by enzyme addition and measured after 10 mins by Glo-lum...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61949 (KSC-4-295 | KUC105342N | N-(3-bromophenyl)-2-(3-ke...) Show SMILES Brc1cccc(NC(=O)Cn2sc3ccccc3c2=O)c1 Show InChI InChI=1S/C15H11BrN2O2S/c16-10-4-3-5-11(8-10)17-14(19)9-18-15(20)12-6-1-2-7-13(12)21-18/h1-8H,9H2,(H,17,19)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Histone deacetylase 6 (Homo sapiens (Human))	BDBM50585748 (CHEMBL5086240) Show SMILES CC(C)(C)OC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)OC(C)(C)C Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of HDAC6 in human DU-145 cells assessed as increase in histone H3 acetylation after 24 hrs by immunofluorescence microscopy				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61957 (3-(3-keto-1,2-benzothiazol-2-yl)-N-phenyl-propiona...) Show SMILES O=C(CCn1sc2ccccc2c1=O)Nc1ccccc1 Show InChI InChI=1S/C16H14N2O2S/c19-15(17-12-6-2-1-3-7-12)10-11-18-16(20)13-8-4-5-9-14(13)21-18/h1-9H,10-11H2,(H,17,19)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
DNA polymerase alpha catalytic subunit (Homo sapiens (Human))	BDBM50090910 (3alpha,16,17,18-tetrahydroxyaphidicolone | 6,13-di...) Show SMILES C[C@@]1(CO)[C@H](O)CC[C@@]2(C)[C@H]1CC[C@H]1C[C@@H]3C[C@]21CC[C@]3(O)CO |r| Show InChI InChI=1S/C20H34O4/c1-17(11-21)15-4-3-13-9-14-10-19(13,7-8-20(14,24)12-22)18(15,2)6-5-16(17)23/h13-16,21-24H,3-12H2,1-2H3/t13-,14+,15-,16+,17-,18-,19-,20-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	1.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
303A College Road East Curated by ChEMBL					Assay Description Inhibition of human DNA polymerase alpha assessed as incorporation of [alpha-32P]dCTP up to 1mM preincubated for 30 mins by whatman DE81 paper bindin...				Antimicrob Agents Chemother 54: 3187-96 (2010) Article DOI: 10.1128/AAC.00399-10 BindingDB Entry DOI: 10.7270/Q2G1614S
					More data for this Ligand-Target Pair				3D Structure (crystal)
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585744 (CHEMBL5081652) Show SMILES CCCC[C@@H](NC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)N[C@H](CCCC)C(=O)OC)C(=O)OC |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 preincubated for 20 mins with DTT followed by enzyme addition and measured after 10 mins by Glo-lum...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585746 (CHEMBL5085306) Show SMILES CC(C)(C)NC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)NC(C)(C)C Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 preincubated for 20 mins with DTT followed by enzyme addition and measured after 10 mins by Glo-lum...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM123128 (1‐(4‐bromo‐2‐nitrophenyl)p...) Show SMILES [O-][N+](=O)c1cc(Br)ccc1N1C(=O)C=CC1=O |c:14| Show InChI InChI=1S/C10H5BrN2O4/c11-6-1-2-7(8(5-6)13(16)17)12-9(14)3-4-10(12)15/h1-5H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.20E+4	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM123129 (1-(3-nitro-phenyl)-pyrrole-2,5-dione (17) | CID236...) Show SMILES [O-][N+](=O)c1cccc(c1)N1C(=O)C=CC1=O |c:13| Show InChI InChI=1S/C10H6N2O4/c13-9-4-5-10(14)11(9)7-2-1-3-8(6-7)12(15)16/h1-6H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.30E+4	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585745 (CHEMBL5084611) Show SMILES OC(CC(=O)Nc1ccccc1)\C=C\CCSSCC\C=C\C(O)CC(=O)Nc1ccccc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 preincubated for 20 mins with DTT followed by enzyme addition and measured after 10 mins by Glo-lum...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61961 (2-(3-keto-1,2-benzothiazol-2-yl)-N-[2-(trifluorome...) Show SMILES FC(F)(F)c1ccccc1NC(=O)Cn1sc2ccccc2c1=O Show InChI InChI=1S/C16H11F3N2O2S/c17-16(18,19)11-6-2-3-7-12(11)20-14(22)9-21-15(23)10-5-1-4-8-13(10)24-21/h1-8H,9H2,(H,20,22)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.80E+4	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585747 (CHEMBL5074871) Show SMILES OC(CC(O)=O)\C=C\CCSSCC\C=C\C(O)CC(O)=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 preincubated for 20 mins with DTT followed by enzyme addition and measured after 10 mins by Glo-lum...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM123130 (1-(2-bromo-4-methylphenyl)-1H-pyrrole-2,5-dione (1...) Show SMILES Cc1ccc(N2C(=O)C=CC2=O)c(Br)c1 |c:8| Show InChI InChI=1S/C11H8BrNO2/c1-7-2-3-9(8(12)6-7)13-10(14)4-5-11(13)15/h2-6H,1H3	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.30E+4	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
DNA polymerase subunit gamma-1 (Homo sapiens (Human))	BDBM50333127 ((beta-D-2',3'-dideoxy-5'-F-cytidine-5'-triphosphat...) Show SMILES Nc1ccn([C@H]2CC[C@H](O2)[C@@H](F)OP(O)(=O)OP(O)(=O)OP(O)(O)=O)c(=O)n1 |r| Show InChI InChI=1S/C9H15FN3O12P3/c10-8(23-27(18,19)25-28(20,21)24-26(15,16)17)5-1-2-7(22-5)13-4-3-6(11)12-9(13)14/h3-5,7-8H,1-2H2,(H,18,19)(H,20,21)(H2,11,12,14)(H2,15,16,17)/t5-,7+,8-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
303A College Road East Curated by ChEMBL					Assay Description Inhibition of human DNA polymerase gamma assessed as incorporation of [alpha-32P]dCTP up to 1mM preincubated for 30 mins by whatman DE81 paper bindin...				Antimicrob Agents Chemother 54: 3187-96 (2010) Article DOI: 10.1128/AAC.00399-10 BindingDB Entry DOI: 10.7270/Q2G1614S
					More data for this Ligand-Target Pair
DNA polymerase subunit gamma-1 (Homo sapiens (Human))	BDBM50090910 (3alpha,16,17,18-tetrahydroxyaphidicolone | 6,13-di...) Show SMILES C[C@@]1(CO)[C@H](O)CC[C@@]2(C)[C@H]1CC[C@H]1C[C@@H]3C[C@]21CC[C@]3(O)CO |r| Show InChI InChI=1S/C20H34O4/c1-17(11-21)15-4-3-13-9-14-10-19(13,7-8-20(14,24)12-22)18(15,2)6-5-16(17)23/h13-16,21-24H,3-12H2,1-2H3/t13-,14+,15-,16+,17-,18-,19-,20-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
303A College Road East Curated by ChEMBL					Assay Description Inhibition of human DNA polymerase gamma assessed as incorporation of [alpha-32P]dCTP up to 1mM preincubated for 30 mins by whatman DE81 paper bindin...				Antimicrob Agents Chemother 54: 3187-96 (2010) Article DOI: 10.1128/AAC.00399-10 BindingDB Entry DOI: 10.7270/Q2G1614S
					More data for this Ligand-Target Pair
DNA polymerase beta (Homo sapiens (Human))	BDBM50090910 (3alpha,16,17,18-tetrahydroxyaphidicolone | 6,13-di...) Show SMILES C[C@@]1(CO)[C@H](O)CC[C@@]2(C)[C@H]1CC[C@H]1C[C@@H]3C[C@]21CC[C@]3(O)CO |r| Show InChI InChI=1S/C20H34O4/c1-17(11-21)15-4-3-13-9-14-10-19(13,7-8-20(14,24)12-22)18(15,2)6-5-16(17)23/h13-16,21-24H,3-12H2,1-2H3/t13-,14+,15-,16+,17-,18-,19-,20-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
303A College Road East Curated by ChEMBL					Assay Description Inhibition of human DNA polymerase beta assessed as incorporation of [alpha-32P]dCTP up to 1mM preincubated for 30 mins by whatman DE81 paper binding...				Antimicrob Agents Chemother 54: 3187-96 (2010) Article DOI: 10.1128/AAC.00399-10 BindingDB Entry DOI: 10.7270/Q2G1614S
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM50247587 (2,5-diphenylisothiazol-3(2H)-one | CHEMBL500224 | ...) Show SMILES O=c1cc(sn1-c1ccccc1)-c1ccccc1 Show InChI InChI=1S/C15H11NOS/c17-15-11-14(12-7-3-1-4-8-12)18-16(15)13-9-5-2-6-10-13/h1-11H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM61938 (1-methyl-2-phenyl-3-indazolone | 1-methyl-2-phenyl...) Show SMILES Cn1n(-c2ccccc2)c(=O)c2ccccc12 Show InChI InChI=1S/C14H12N2O/c1-15-13-10-6-5-9-12(13)14(17)16(15)11-7-3-2-4-8-11/h2-10H,1H3	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585748 (CHEMBL5086240) Show SMILES CC(C)(C)OC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)OC(C)(C)C Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 incubated for 10 mins by Glo-luminescence assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585746 (CHEMBL5085306) Show SMILES CC(C)(C)NC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)NC(C)(C)C Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 incubated for 10 mins by Glo-luminescence assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585745 (CHEMBL5084611) Show SMILES OC(CC(=O)Nc1ccccc1)\C=C\CCSSCC\C=C\C(O)CC(=O)Nc1ccccc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.05E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 incubated for 10 mins by Glo-luminescence assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585743 (CHEMBL5087342) Show SMILES CCCC[C@@H](NC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)N[C@H](CCCC)C(O)=O)C(O)=O |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.40E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 incubated for 10 mins by Glo-luminescence assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585747 (CHEMBL5074871) Show SMILES OC(CC(O)=O)\C=C\CCSSCC\C=C\C(O)CC(O)=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.40E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 incubated for 10 mins by Glo-luminescence assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
Histone deacetylase 2 (Homo sapiens (Human))	BDBM50585744 (CHEMBL5081652) Show SMILES CCCC[C@@H](NC(=O)CC(O)\C=C\CCSSCC\C=C\C(O)CC(=O)N[C@H](CCCC)C(=O)OC)C(=O)OC |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.80E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human full-length HDAC2 incubated for 10 mins by Glo-luminescence assay				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c01928 BindingDB Entry DOI: 10.7270/Q2H41WB8
					More data for this Ligand-Target Pair
DNA-directed RNA polymerase II subunit RPB1 (Homo sapiens (Human))	BDBM50333129 (((2R,3R,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1...) Show SMILES C[C@@]1(F)[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]1n1ccc(=O)[nH]c1=O |r| Show InChI InChI=1S/C10H16FN2O14P3/c1-10(11)7(15)5(25-8(10)13-3-2-6(14)12-9(13)16)4-24-29(20,21)27-30(22,23)26-28(17,18)19/h2-3,5,7-8,15H,4H2,1H3,(H,20,21)(H,22,23)(H,12,14,16)(H2,17,18,19)/t5-,7-,8-,10-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
303A College Road East Curated by ChEMBL					Assay Description Inhibition of human RNA polymerase 2				Antimicrob Agents Chemother 54: 3187-96 (2010) Article DOI: 10.1128/AAC.00399-10 BindingDB Entry DOI: 10.7270/Q2G1614S
					More data for this Ligand-Target Pair
DNA-directed RNA polymerase II subunit RPB1 (Homo sapiens (Human))	BDBM50333128 (((2S,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-4-...) Show SMILES Nc1ccn([C@@H]2O[C@H](CO[P@@](O)(=O)O[P@@](O)(=O)OP(O)(O)=O)C[C@H]2O)c(=O)n1 |r| Show InChI InChI=1S/C9H16N3O13P3/c10-7-1-2-12(9(14)11-7)8-6(13)3-5(23-8)4-22-27(18,19)25-28(20,21)24-26(15,16)17/h1-2,5-6,8,13H,3-4H2,(H,18,19)(H,20,21)(H2,10,11,14)(H2,15,16,17)/t5-,6+,8+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
303A College Road East Curated by ChEMBL					Assay Description Inhibition of human RNA polymerase 2				Antimicrob Agents Chemother 54: 3187-96 (2010) Article DOI: 10.1128/AAC.00399-10 BindingDB Entry DOI: 10.7270/Q2G1614S
					More data for this Ligand-Target Pair
DNA polymerase alpha catalytic subunit (Homo sapiens (Human))	BDBM50333127 ((beta-D-2',3'-dideoxy-5'-F-cytidine-5'-triphosphat...) Show SMILES Nc1ccn([C@H]2CC[C@H](O2)[C@@H](F)OP(O)(=O)OP(O)(=O)OP(O)(O)=O)c(=O)n1 |r| Show InChI InChI=1S/C9H15FN3O12P3/c10-8(23-27(18,19)25-28(20,21)24-26(15,16)17)5-1-2-7(22-5)13-4-3-6(11)12-9(13)14/h3-5,7-8H,1-2H2,(H,18,19)(H,20,21)(H2,11,12,14)(H2,15,16,17)/t5-,7+,8-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
303A College Road East Curated by ChEMBL					Assay Description Inhibition of human DNA polymerase alpha assessed as incorporation of [alpha-32P]dCTP up to 1mM preincubated for 30 mins by whatman DE81 paper bindin...				Antimicrob Agents Chemother 54: 3187-96 (2010) Article DOI: 10.1128/AAC.00399-10 BindingDB Entry DOI: 10.7270/Q2G1614S
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus)	BDBM50220832 (CHEMBL8211 | N-ethylmaleimide) Show SMILES CCN1C(=O)C=CC1=O |c:5| Show InChI InChI=1S/C6H7NO2/c1-2-7-5(8)3-4-6(7)9/h3-4H,2H2,1H3	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	5.30E+5	n/a	n/a	n/a	n/a	7.5	23
University of Wisconsin-Milwaukee					Assay Description Binding assays containing 25 mM MOPS pH 7.5, 1.25 mM MgCl2, 20 nM Cy5-dT15, and 200 nM NS3h_1b were incubated 5 min at RT. Following addition of indi...				ACS Chem Biol 9: 2393-2403 (2014) Article DOI: 10.1021/cb500512z BindingDB Entry DOI: 10.7270/Q2G15ZHH
					More data for this Ligand-Target Pair
DNA polymerase alpha catalytic subunit (Homo sapiens (Human))	BDBM50333129 (((2R,3R,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1...) Show SMILES C[C@@]1(F)[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]1n1ccc(=O)[nH]c1=O |r| Show InChI InChI=1S/C10H16FN2O14P3/c1-10(11)7(15)5(25-8(10)13-3-2-6(14)12-9(13)16)4-24-29(20,21)27-30(22,23)26-28(17,18)19/h2-3,5,7-8,15H,4H2,1H3,(H,20,21)(H,22,23)(H,12,14,16)(H2,17,18,19)/t5-,7-,8-,10-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
303A College Road East Curated by ChEMBL					Assay Description Inhibition of human DNA polymerase alpha assessed as incorporation of [alpha-32P]dCTP up to 1mM preincubated for 30 mins by whatman DE81 paper bindin...				Antimicrob Agents Chemother 54: 3187-96 (2010) Article DOI: 10.1128/AAC.00399-10 BindingDB Entry DOI: 10.7270/Q2G1614S
					More data for this Ligand-Target Pair

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