Compile Data Set for Download or QSAR

Found 73 hits Enz. Inhib. hit(s) with Target = 'Bile salt-activated lipase'   

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
Bile salt-activated lipase (Homo sapiens (Human))	BDBM50081700 (6-Chloro-3-(2-cyclohexyl-ethyl)-pyran-2-one | CHEM...) Show SMILES Clc1ccc(CCC2CCCCC2)c(=O)o1 Show InChI InChI=1S/C13H17ClO2/c14-12-9-8-11(13(15)16-12)7-6-10-4-2-1-3-5-10/h8-10H,1-7H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	25	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of New Mexico Curated by ChEMBL					Assay Description Inhibition of the Pancreatic Cholesterol Esterase from porcine				J Med Chem 42: 4250-6 (1999) BindingDB Entry DOI: 10.7270/Q2KP81C5
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Homo sapiens (Human))	BDBM50081696 (6-Chloro-3-cyclopentyl-pyran-2-one | CHEMBL133091) Show SMILES Clc1ccc(C2CCCC2)c(=O)o1 Show InChI InChI=1S/C10H11ClO2/c11-9-6-5-8(10(12)13-9)7-3-1-2-4-7/h5-7H,1-4H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of New Mexico Curated by ChEMBL					Assay Description Inhibition of the Pancreatic Cholesterol Esterase from porcine				J Med Chem 42: 4250-6 (1999) BindingDB Entry DOI: 10.7270/Q2KP81C5
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Homo sapiens (Human))	BDBM50081698 (6-Chloro-5-(2-cyclohexyl-ethyl)-pyran-2-one | CHEM...) Show SMILES Clc1oc(=O)ccc1CCC1CCCCC1 Show InChI InChI=1S/C13H17ClO2/c14-13-11(8-9-12(15)16-13)7-6-10-4-2-1-3-5-10/h8-10H,1-7H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	58	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of New Mexico Curated by ChEMBL					Assay Description Inhibition of the Pancreatic Cholesterol Esterase from porcine				J Med Chem 42: 4250-6 (1999) BindingDB Entry DOI: 10.7270/Q2KP81C5
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Homo sapiens (Human))	BDBM50081697 (6-Chloro-3-(3-cyclohexyl-propyl)-pyran-2-one | CHE...) Show SMILES Clc1ccc(CCCC2CCCCC2)c(=O)o1 Show InChI InChI=1S/C14H19ClO2/c15-13-10-9-12(14(16)17-13)8-4-7-11-5-2-1-3-6-11/h9-11H,1-8H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of New Mexico Curated by ChEMBL					Assay Description Inhibition of the Pancreatic Cholesterol Esterase from porcine				J Med Chem 42: 4250-6 (1999) BindingDB Entry DOI: 10.7270/Q2KP81C5
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Homo sapiens (Human))	BDBM50081695 (6-Chloro-3-(4-cyclohexyl-butyl)-pyran-2-one | CHEM...) Show SMILES Clc1ccc(CCCCC2CCCCC2)c(=O)o1 Show InChI InChI=1S/C15H21ClO2/c16-14-11-10-13(15(17)18-14)9-5-4-8-12-6-2-1-3-7-12/h10-12H,1-9H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	580	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of New Mexico Curated by ChEMBL					Assay Description Inhibition of the Pancreatic Cholesterol Esterase from porcine				J Med Chem 42: 4250-6 (1999) BindingDB Entry DOI: 10.7270/Q2KP81C5
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50084233 (2-Diethylamino-6,7-dihydro-5H-cyclopenta[4,5]thien...) Show SMILES CCN(CC)c1nc2sc3CCCc3c2c(=O)o1 Show InChI InChI=1S/C13H16N2O2S/c1-3-15(4-2)13-14-11-10(12(16)17-13)8-6-5-7-9(8)18-11/h3-7H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	580	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179322 (6,7-dihydro-2-(dimethylamino)-4H,5H-cyclopenta[4,5...) Show SMILES CN(C)c1nc2sc3CCCc3c2c(=O)o1 Show InChI InChI=1S/C11H12N2O2S/c1-13(2)11-12-9-8(10(14)15-11)6-4-3-5-7(6)16-9/h3-5H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	630	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50286878 (Butyl-carbamic acid 2'-hydroxy-[1,1']binaphthaleny...) Show SMILES CCCCNC(=O)Oc1ccc2ccccc2c1-c1c(O)ccc2ccccc12 |(-5.4,-.57,;-4.07,-1.34,;-2.73,-.57,;-1.4,-1.35,;-.06,-.57,;1.27,-1.35,;1.27,-2.89,;2.61,-.58,;3.94,-1.35,;3.94,-2.89,;5.28,-3.66,;6.6,-2.89,;7.93,-3.66,;9.28,-2.89,;9.28,-1.35,;7.95,-.57,;6.6,-1.35,;5.28,-.58,;5.28,.96,;6.6,1.74,;7.93,.97,;6.6,3.28,;5.25,4.05,;3.94,3.26,;2.59,4.03,;1.27,3.26,;1.27,1.72,;2.59,.95,;3.94,1.72,)| Show InChI InChI=1S/C25H23NO3/c1-2-3-16-26-25(28)29-22-15-13-18-9-5-7-11-20(18)24(22)23-19-10-6-4-8-17(19)12-14-21(23)27/h4-15,27H,2-3,16H2,1H3,(H,26,28)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	800	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Dissociation constant of the compound (KI) for the Pancreatic cholesterol esterase-catalyzed hydrolysis of 4-nitrophenyl butyrate				Bioorg Med Chem Lett 6: 43-46 (1996) Article DOI: 10.1016/0960-894X(95)00549-9 BindingDB Entry DOI: 10.7270/Q2RV0NPW
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50286878 (Butyl-carbamic acid 2'-hydroxy-[1,1']binaphthaleny...) Show SMILES CCCCNC(=O)Oc1ccc2ccccc2c1-c1c(O)ccc2ccccc12 |(-5.4,-.57,;-4.07,-1.34,;-2.73,-.57,;-1.4,-1.35,;-.06,-.57,;1.27,-1.35,;1.27,-2.89,;2.61,-.58,;3.94,-1.35,;3.94,-2.89,;5.28,-3.66,;6.6,-2.89,;7.93,-3.66,;9.28,-2.89,;9.28,-1.35,;7.95,-.57,;6.6,-1.35,;5.28,-.58,;5.28,.96,;6.6,1.74,;7.93,.97,;6.6,3.28,;5.25,4.05,;3.94,3.26,;2.59,4.03,;1.27,3.26,;1.27,1.72,;2.59,.95,;3.94,1.72,)| Show InChI InChI=1S/C25H23NO3/c1-2-3-16-26-25(28)29-22-15-13-18-9-5-7-11-20(18)24(22)23-19-10-6-4-8-17(19)12-14-21(23)27/h4-15,27H,2-3,16H2,1H3,(H,26,28)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	800	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Vascular endothelial growth factor receptor 2 (KDR)				Bioorg Med Chem Lett 6: 43-46 (1996) Article DOI: 10.1016/0960-894X(95)00549-9 BindingDB Entry DOI: 10.7270/Q2RV0NPW
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50286878 (Butyl-carbamic acid 2'-hydroxy-[1,1']binaphthaleny...) Show SMILES CCCCNC(=O)Oc1ccc2ccccc2c1-c1c(O)ccc2ccccc12 |(-5.4,-.57,;-4.07,-1.34,;-2.73,-.57,;-1.4,-1.35,;-.06,-.57,;1.27,-1.35,;1.27,-2.89,;2.61,-.58,;3.94,-1.35,;3.94,-2.89,;5.28,-3.66,;6.6,-2.89,;7.93,-3.66,;9.28,-2.89,;9.28,-1.35,;7.95,-.57,;6.6,-1.35,;5.28,-.58,;5.28,.96,;6.6,1.74,;7.93,.97,;6.6,3.28,;5.25,4.05,;3.94,3.26,;2.59,4.03,;1.27,3.26,;1.27,1.72,;2.59,.95,;3.94,1.72,)| Show InChI InChI=1S/C25H23NO3/c1-2-3-16-26-25(28)29-22-15-13-18-9-5-7-11-20(18)24(22)23-19-10-6-4-8-17(19)12-14-21(23)27/h4-15,27H,2-3,16H2,1H3,(H,26,28)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	800	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Vascular endothelial growth factor receptor 2 (KDR)				Bioorg Med Chem Lett 6: 43-46 (1996) Article DOI: 10.1016/0960-894X(95)00549-9 BindingDB Entry DOI: 10.7270/Q2RV0NPW
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50084229 (2-Diethylamino-5-methyl-5,6,7,8-tetrahydro-benzo[4...) Show SMILES CCN(CC)c1nc2sc3CCCC(C)c3c2c(=O)o1 Show InChI InChI=1S/C15H20N2O2S/c1-4-17(5-2)15-16-13-12(14(18)19-15)11-9(3)7-6-8-10(11)20-13/h9H,4-8H2,1-3H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.64E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50064308 (2-Diethylamino-5,6,7,8-tetrahydro-benzo[4,5]thieno...) Show SMILES CCN(CC)c1nc2sc3CCCCc3c2c(=O)o1 Show InChI InChI=1S/C14H18N2O2S/c1-3-16(4-2)14-15-12-11(13(17)18-14)9-7-5-6-8-10(9)19-12/h3-8H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.86E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179331 (5,6,7,8-tetrahydro-2-(dimethylamino)-4H-benzo[4,5]...) Show SMILES CN(C)c1nc2sc3CCCCc3c2c(=O)o1 Show InChI InChI=1S/C12H14N2O2S/c1-14(2)12-13-10-9(11(15)16-12)7-5-3-4-6-8(7)17-10/h3-6H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.15E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Homo sapiens (Human))	BDBM50081694 (6-Chloro-3-cyclohexylmethyl-pyran-2-one | CHEMBL44...) Show SMILES Clc1ccc(CC2CCCCC2)c(=O)o1 Show InChI InChI=1S/C12H15ClO2/c13-11-7-6-10(12(14)15-11)8-9-4-2-1-3-5-9/h6-7,9H,1-5,8H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of New Mexico Curated by ChEMBL					Assay Description Inhibition of the Pancreatic Cholesterol Esterase from porcine				J Med Chem 42: 4250-6 (1999) BindingDB Entry DOI: 10.7270/Q2KP81C5
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Homo sapiens (Human))	BDBM50081699 (6-Chloro-3-cyclohexyl-pyran-2-one | CHEMBL134790) Show SMILES Clc1ccc(C2CCCCC2)c(=O)o1 Show InChI InChI=1S/C11H13ClO2/c12-10-7-6-9(11(13)14-10)8-4-2-1-3-5-8/h6-8H,1-5H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of New Mexico Curated by ChEMBL					Assay Description Inhibition of the Pancreatic Cholesterol Esterase from porcine				J Med Chem 42: 4250-6 (1999) BindingDB Entry DOI: 10.7270/Q2KP81C5
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179326 (2-(diethylamino)-5,6-dimethyl-4H-thieno[2,3-d][1,3...) Show SMILES CCN(CC)c1nc2sc(C)c(C)c2c(=O)o1 Show InChI InChI=1S/C12H16N2O2S/c1-5-14(6-2)12-13-10-9(11(15)16-12)7(3)8(4)17-10/h5-6H2,1-4H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179329 (2-morpholin-4-yl-5,6,7,8-tetrahydro-benzo[4,5]thie...) Show SMILES O=c1oc(nc2sc3CCCCc3c12)N1CCOCC1 Show InChI InChI=1S/C14H16N2O3S/c17-13-11-9-3-1-2-4-10(9)20-12(11)15-14(19-13)16-5-7-18-8-6-16/h1-8H2	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179318 (2-dimethylamino-5,8-dihydro-4H,6H-thiopyrano[4',3'...) Show SMILES CN(C)c1nc2sc3CSCCc3c2c(=O)o1 Show InChI InChI=1S/C11H12N2O2S2/c1-13(2)11-12-9-8(10(14)15-11)6-3-4-16-5-7(6)17-9/h3-5H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	5.76E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50084234 (2-Diethylamino-6,7,8,9-tetrahydro-5H-3-oxa-10-thia...) Show SMILES CCN(CC)c1nc2sc3CCCCCc3c2c(=O)o1 Show InChI InChI=1S/C15H20N2O2S/c1-3-17(4-2)15-16-13-12(14(18)19-15)10-8-6-5-7-9-11(10)20-13/h3-9H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50084232 (2-(diethylamino)-5-isopropyl-4H-thieno[2,3-d][1,3]...) Show SMILES CCN(CC)c1nc2scc(C(C)C)c2c(=O)o1 Show InChI InChI=1S/C13H18N2O2S/c1-5-15(6-2)13-14-11-10(12(16)17-13)9(7-18-11)8(3)4/h7-8H,5-6H2,1-4H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50084235 (2-Diethylamino-benzo[4,5]thieno[2,3-d][1,3]oxazin-...) Show SMILES CCN(CC)c1nc2sc3ccccc3c2c(=O)o1 Show InChI InChI=1S/C14H14N2O2S/c1-3-16(4-2)14-15-12-11(13(17)18-14)9-7-5-6-8-10(9)19-12/h5-8H,3-4H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.50E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50286880 (Butyric acid 2'-butylcarbamoyloxy-[1,1']binaphthal...) Show SMILES CCCCNC(=O)Oc1ccc2ccccc2c1-c1c(OC(=O)CCC)ccc2ccccc12 |(-5.23,-.68,;-3.9,-1.45,;-2.56,-.68,;-1.23,-1.47,;.12,-.68,;1.45,-1.47,;1.45,-3.01,;2.78,-.7,;4.11,-1.47,;4.11,-3.01,;5.44,-3.78,;6.79,-3.01,;8.12,-3.78,;9.46,-3.01,;9.46,-1.47,;8.13,-.68,;6.79,-1.47,;5.44,-.7,;5.44,.84,;6.77,1.63,;8.12,.86,;9.45,1.63,;9.43,3.17,;10.79,.86,;12.12,1.65,;13.45,.88,;6.77,3.17,;5.44,3.94,;4.11,3.15,;2.78,3.92,;1.45,3.15,;1.45,1.6,;2.78,.83,;4.11,1.61,)| Show InChI InChI=1S/C29H29NO4/c1-3-5-19-30-29(32)34-25-18-16-21-12-7-9-14-23(21)28(25)27-22-13-8-6-11-20(22)15-17-24(27)33-26(31)10-4-2/h6-9,11-18H,3-5,10,19H2,1-2H3,(H,30,32)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Vascular endothelial growth factor receptor 2 (KDR)				Bioorg Med Chem Lett 6: 43-46 (1996) Article DOI: 10.1016/0960-894X(95)00549-9 BindingDB Entry DOI: 10.7270/Q2RV0NPW
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50084228 (2-(diethylamino)-5-methyl-4H-thieno[2,3-d][1,3]oxa...) Show SMILES CCN(CC)c1nc2scc(C)c2c(=O)o1 Show InChI InChI=1S/C11H14N2O2S/c1-4-13(5-2)11-12-9-8(10(14)15-11)7(3)6-16-9/h6H,4-5H2,1-3H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179311 (2-(cyclohexyl-methyl-amino)-5,6,7,8-tetrahydro-ben...) Show SMILES CN(C1CCCCC1)c1nc2sc3CCCCc3c2c(=O)o1 Show InChI InChI=1S/C17H22N2O2S/c1-19(11-7-3-2-4-8-11)17-18-15-14(16(20)21-17)12-9-5-6-10-13(12)22-15/h11H,2-10H2,1H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.80E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50286880 (Butyric acid 2'-butylcarbamoyloxy-[1,1']binaphthal...) Show SMILES CCCCNC(=O)Oc1ccc2ccccc2c1-c1c(OC(=O)CCC)ccc2ccccc12 |(-5.23,-.68,;-3.9,-1.45,;-2.56,-.68,;-1.23,-1.47,;.12,-.68,;1.45,-1.47,;1.45,-3.01,;2.78,-.7,;4.11,-1.47,;4.11,-3.01,;5.44,-3.78,;6.79,-3.01,;8.12,-3.78,;9.46,-3.01,;9.46,-1.47,;8.13,-.68,;6.79,-1.47,;5.44,-.7,;5.44,.84,;6.77,1.63,;8.12,.86,;9.45,1.63,;9.43,3.17,;10.79,.86,;12.12,1.65,;13.45,.88,;6.77,3.17,;5.44,3.94,;4.11,3.15,;2.78,3.92,;1.45,3.15,;1.45,1.6,;2.78,.83,;4.11,1.61,)| Show InChI InChI=1S/C29H29NO4/c1-3-5-19-30-29(32)34-25-18-16-21-12-7-9-14-23(21)28(25)27-22-13-8-6-11-20(22)15-17-24(27)33-26(31)10-4-2/h6-9,11-18H,3-5,10,19H2,1-2H3,(H,30,32)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Vascular endothelial growth factor receptor 2 (KDR)				Bioorg Med Chem Lett 6: 43-46 (1996) Article DOI: 10.1016/0960-894X(95)00549-9 BindingDB Entry DOI: 10.7270/Q2RV0NPW
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50286880 (Butyric acid 2'-butylcarbamoyloxy-[1,1']binaphthal...) Show SMILES CCCCNC(=O)Oc1ccc2ccccc2c1-c1c(OC(=O)CCC)ccc2ccccc12 |(-5.23,-.68,;-3.9,-1.45,;-2.56,-.68,;-1.23,-1.47,;.12,-.68,;1.45,-1.47,;1.45,-3.01,;2.78,-.7,;4.11,-1.47,;4.11,-3.01,;5.44,-3.78,;6.79,-3.01,;8.12,-3.78,;9.46,-3.01,;9.46,-1.47,;8.13,-.68,;6.79,-1.47,;5.44,-.7,;5.44,.84,;6.77,1.63,;8.12,.86,;9.45,1.63,;9.43,3.17,;10.79,.86,;12.12,1.65,;13.45,.88,;6.77,3.17,;5.44,3.94,;4.11,3.15,;2.78,3.92,;1.45,3.15,;1.45,1.6,;2.78,.83,;4.11,1.61,)| Show InChI InChI=1S/C29H29NO4/c1-3-5-19-30-29(32)34-25-18-16-21-12-7-9-14-23(21)28(25)27-22-13-8-6-11-20(22)15-17-24(27)33-26(31)10-4-2/h6-9,11-18H,3-5,10,19H2,1-2H3,(H,30,32)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Dissociation constant of the compound (KI) for the Pancreatic cholesterol esterase-catalyzed hydrolysis of 4-nitrophenyl butyrate				Bioorg Med Chem Lett 6: 43-46 (1996) Article DOI: 10.1016/0960-894X(95)00549-9 BindingDB Entry DOI: 10.7270/Q2RV0NPW
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50286879 (Butyl-carbamic acid 2'-butylcarbamoyloxy-[1,1']bin...) Show SMILES CCCCNC(=O)Oc1ccc2ccccc2c1-c1c(OC(=O)NCCCC)ccc2ccccc12 |(16.13,.89,;14.79,1.65,;13.46,.88,;12.12,1.65,;10.79,.86,;9.45,1.63,;9.43,3.17,;8.12,.86,;6.77,1.63,;6.77,3.17,;5.44,3.94,;4.11,3.15,;2.78,3.92,;1.45,3.15,;1.45,1.6,;2.78,.83,;4.11,1.61,;5.44,.84,;5.44,-.7,;4.11,-1.47,;2.78,-.7,;1.45,-1.47,;1.45,-3.01,;.12,-.68,;-1.23,-1.47,;-2.56,-.68,;-3.9,-1.45,;-5.23,-.68,;4.11,-3.01,;5.44,-3.78,;6.79,-3.01,;8.12,-3.78,;9.46,-3.01,;9.46,-1.47,;8.13,-.68,;6.79,-1.47,)| Show InChI InChI=1S/C30H32N2O4/c1-3-5-19-31-29(33)35-25-17-15-21-11-7-9-13-23(21)27(25)28-24-14-10-8-12-22(24)16-18-26(28)36-30(34)32-20-6-4-2/h7-18H,3-6,19-20H2,1-2H3,(H,31,33)(H,32,34)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	2.90E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Vascular endothelial growth factor receptor 2 (KDR)				Bioorg Med Chem Lett 6: 43-46 (1996) Article DOI: 10.1016/0960-894X(95)00549-9 BindingDB Entry DOI: 10.7270/Q2RV0NPW
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50286879 (Butyl-carbamic acid 2'-butylcarbamoyloxy-[1,1']bin...) Show SMILES CCCCNC(=O)Oc1ccc2ccccc2c1-c1c(OC(=O)NCCCC)ccc2ccccc12 |(16.13,.89,;14.79,1.65,;13.46,.88,;12.12,1.65,;10.79,.86,;9.45,1.63,;9.43,3.17,;8.12,.86,;6.77,1.63,;6.77,3.17,;5.44,3.94,;4.11,3.15,;2.78,3.92,;1.45,3.15,;1.45,1.6,;2.78,.83,;4.11,1.61,;5.44,.84,;5.44,-.7,;4.11,-1.47,;2.78,-.7,;1.45,-1.47,;1.45,-3.01,;.12,-.68,;-1.23,-1.47,;-2.56,-.68,;-3.9,-1.45,;-5.23,-.68,;4.11,-3.01,;5.44,-3.78,;6.79,-3.01,;8.12,-3.78,;9.46,-3.01,;9.46,-1.47,;8.13,-.68,;6.79,-1.47,)| Show InChI InChI=1S/C30H32N2O4/c1-3-5-19-31-29(33)35-25-17-15-21-11-7-9-13-23(21)27(25)28-24-14-10-8-12-22(24)16-18-26(28)36-30(34)32-20-6-4-2/h7-18H,3-6,19-20H2,1-2H3,(H,31,33)(H,32,34)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Vascular endothelial growth factor receptor 2 (KDR)				Bioorg Med Chem Lett 6: 43-46 (1996) Article DOI: 10.1016/0960-894X(95)00549-9 BindingDB Entry DOI: 10.7270/Q2RV0NPW
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50286879 (Butyl-carbamic acid 2'-butylcarbamoyloxy-[1,1']bin...) Show SMILES CCCCNC(=O)Oc1ccc2ccccc2c1-c1c(OC(=O)NCCCC)ccc2ccccc12 |(16.13,.89,;14.79,1.65,;13.46,.88,;12.12,1.65,;10.79,.86,;9.45,1.63,;9.43,3.17,;8.12,.86,;6.77,1.63,;6.77,3.17,;5.44,3.94,;4.11,3.15,;2.78,3.92,;1.45,3.15,;1.45,1.6,;2.78,.83,;4.11,1.61,;5.44,.84,;5.44,-.7,;4.11,-1.47,;2.78,-.7,;1.45,-1.47,;1.45,-3.01,;.12,-.68,;-1.23,-1.47,;-2.56,-.68,;-3.9,-1.45,;-5.23,-.68,;4.11,-3.01,;5.44,-3.78,;6.79,-3.01,;8.12,-3.78,;9.46,-3.01,;9.46,-1.47,;8.13,-.68,;6.79,-1.47,)| Show InChI InChI=1S/C30H32N2O4/c1-3-5-19-31-29(33)35-25-17-15-21-11-7-9-13-23(21)27(25)28-24-14-10-8-12-22(24)16-18-26(28)36-30(34)32-20-6-4-2/h7-18H,3-6,19-20H2,1-2H3,(H,31,33)(H,32,34)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Vascular endothelial growth factor receptor 2 (KDR)				Bioorg Med Chem Lett 6: 43-46 (1996) Article DOI: 10.1016/0960-894X(95)00549-9 BindingDB Entry DOI: 10.7270/Q2RV0NPW
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179315 (7-benzyl-2-diethylamino-5,6,7,8-tetrahydro-4H-pyri...) Show SMILES CCN(CC)c1nc2sc3CN(Cc4ccccc4)CCc3c2c(=O)o1 Show InChI InChI=1S/C20H23N3O2S/c1-3-23(4-2)20-21-18-17(19(24)25-20)15-10-11-22(13-16(15)26-18)12-14-8-6-5-7-9-14/h5-9H,3-4,10-13H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179308 (7-benzyl-5,6,7,8-tetrahydro-2-(morpholin-4-yl)-4H-...) Show SMILES O=c1oc(nc2sc3CN(Cc4ccccc4)CCc3c12)N1CCOCC1 Show InChI InChI=1S/C20H21N3O3S/c24-19-17-15-6-7-22(12-14-4-2-1-3-5-14)13-16(15)27-18(17)21-20(26-19)23-8-10-25-11-9-23/h1-5H,6-13H2	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50084227 (2-(diethylamino)-5-methyl-4-oxo-4H-thieno[2,3-d][1...) Show SMILES CCN(CC)c1nc2sc(C(N)=O)c(C)c2c(=O)o1 Show InChI InChI=1S/C12H15N3O3S/c1-4-15(5-2)12-14-10-7(11(17)18-12)6(3)8(19-10)9(13)16/h4-5H2,1-3H3,(H2,13,16)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179313 (2-amino-7-benzyl-5,6,7,8-tetrahydro-4H-pyrido[4',3...) Show SMILES Nc1nc2sc3CN(Cc4ccccc4)CCc3c2c(=O)s1 Show InChI InChI=1S/C16H15N3OS2/c17-16-18-14-13(15(20)22-16)11-6-7-19(9-12(11)21-14)8-10-4-2-1-3-5-10/h1-5H,6-9H2,(H2,17,18)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179316 (5,8-dihydro-2-(dimethylamino)-4H,6H-pyrano[4',3':4...) Show SMILES CN(C)c1nc2sc3COCCc3c2c(=O)o1 Show InChI InChI=1S/C11H12N2O3S/c1-13(2)11-12-9-8(10(14)16-11)6-3-4-15-5-7(6)17-9/h3-5H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179319 (7-benzyl-2-cyclohexylamino-5,6,7,8-tetrahydro-4H-p...) Show SMILES O=c1sc(NC2CCCCC2)nc2sc3CN(Cc4ccccc4)CCc3c12 Show InChI InChI=1S/C22H25N3OS2/c26-21-19-17-11-12-25(13-15-7-3-1-4-8-15)14-18(17)27-20(19)24-22(28-21)23-16-9-5-2-6-10-16/h1,3-4,7-8,16H,2,5-6,9-14H2,(H,23,24)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179320 (7-benzyl-5,6,7,8-tetrahydro-2-phenylamino-4H-pyrid...) Show SMILES O=c1sc(Nc2ccccc2)nc2sc3CN(Cc4ccccc4)CCc3c12 Show InChI InChI=1S/C22H19N3OS2/c26-21-19-17-11-12-25(13-15-7-3-1-4-8-15)14-18(17)27-20(19)24-22(28-21)23-16-9-5-2-6-10-16/h1-10H,11-14H2,(H,23,24)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179324 (7-ethyl-5,6,7,8-tetrahydro-2-(dimethylamino)-4H-py...) Show SMILES CCN1CCc2c(C1)sc1nc(oc(=O)c21)N(C)C Show InChI InChI=1S/C13H17N3O2S/c1-4-16-6-5-8-9(7-16)19-11-10(8)12(17)18-13(14-11)15(2)3/h4-7H2,1-3H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179327 (7-benzyl-5,6,7,8-tetrahydro-2-phenylamino-4H-pyrid...) Show SMILES O=c1oc(Nc2ccccc2)nc2sc3CN(Cc4ccccc4)CCc3c12 Show InChI InChI=1S/C22H19N3O2S/c26-21-19-17-11-12-25(13-15-7-3-1-4-8-15)14-18(17)28-20(19)24-22(27-21)23-16-9-5-2-6-10-16/h1-10H,11-14H2,(H,23,24)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179310 (2-amino-7-benzyl-5,6,7,8-tetrahydro-4H-pyrido[4',3...) Show SMILES Nc1nc2sc3CN(Cc4ccccc4)CCc3c2c(=O)o1 Show InChI InChI=1S/C16H15N3O2S/c17-16-18-14-13(15(20)21-16)11-6-7-19(9-12(11)22-14)8-10-4-2-1-3-5-10/h1-5H,6-9H2,(H2,17,18)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50064321 (2-isopropylamino-5,6,7,8-tetrahydro-benzo[4,5]thie...) Show SMILES CC(C)Nc1nc2sc3CCCCc3c2c(=O)o1 Show InChI InChI=1S/C13H16N2O2S/c1-7(2)14-13-15-11-10(12(16)17-13)8-5-3-4-6-9(8)18-11/h7H,3-6H2,1-2H3,(H,14,15)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179330 (2-benzoylamino-7-benzyl-5,6,7,8-tetrahydro-4H-pyri...) Show SMILES O=C(Nc1nc2sc3CN(Cc4ccccc4)CCc3c2c(=O)o1)c1ccccc1 Show InChI InChI=1S/C23H19N3O3S/c27-20(16-9-5-2-6-10-16)24-23-25-21-19(22(28)29-23)17-11-12-26(14-18(17)30-21)13-15-7-3-1-4-8-15/h1-10H,11-14H2,(H,24,25,27)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179328 (7-benzyl-5,6,7,8-tetrahydro-2-[N-3,4-dimethoxy-ben...) Show SMILES COc1ccc(CN(C)c2nc3sc4CN(Cc5ccccc5)CCc4c3c(=O)o2)cc1OC Show InChI InChI=1S/C26H27N3O4S/c1-28(14-18-9-10-20(31-2)21(13-18)32-3)26-27-24-23(25(30)33-26)19-11-12-29(16-22(19)34-24)15-17-7-5-4-6-8-17/h4-10,13H,11-12,14-16H2,1-3H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179332 (7-benzyl-2-cyclohexylamino-5,6,7,8-tetrahydro-4H-p...) Show SMILES O=c1oc(NC2CCCCC2)nc2sc3CN(Cc4ccccc4)CCc3c12 Show InChI InChI=1S/C22H25N3O2S/c26-21-19-17-11-12-25(13-15-7-3-1-4-8-15)14-18(17)28-20(19)24-22(27-21)23-16-9-5-2-6-10-16/h1,3-4,7-8,16H,2,5-6,9-14H2,(H,23,24)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179333 (5,6,7,8-tetrahydro-7-methyl-2-(dimethylamino)-4H-p...) Show SMILES CN(C)c1nc2sc3CN(C)CCc3c2c(=O)o1 Show InChI InChI=1S/C12H15N3O2S/c1-14(2)12-13-10-9(11(16)17-12)7-4-5-15(3)6-8(7)18-10/h4-6H2,1-3H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179323 (2-benzoylamino-7-benzyl-5,6,7,8-tetrahydro-4H-pyri...) Show SMILES O=C(Nc1nc2sc3CN(Cc4ccccc4)CCc3c2c(=O)s1)c1ccccc1 Show InChI InChI=1S/C23H19N3O2S2/c27-20(16-9-5-2-6-10-16)24-23-25-21-19(22(28)30-23)17-11-12-26(14-18(17)29-21)13-15-7-3-1-4-8-15/h1-10H,11-14H2,(H,24,25,27)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179321 (7-benzoyl-5,6,7,8-tetrahydro-2-(dimethylamino)-4H-...) Show SMILES CN(C)c1nc2sc3CN(CCc3c2c(=O)o1)C(=O)c1ccccc1 Show InChI InChI=1S/C18H17N3O3S/c1-20(2)18-19-15-14(17(23)24-18)12-8-9-21(10-13(12)25-15)16(22)11-6-4-3-5-7-11/h3-7H,8-10H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179309 (7-benzyl-5,6,7,8-tetrahydro-2-isopropylamino-4H-py...) Show SMILES CC(C)Nc1nc2sc3CN(Cc4ccccc4)CCc3c2c(=O)s1 Show InChI InChI=1S/C19H21N3OS2/c1-12(2)20-19-21-17-16(18(23)25-19)14-8-9-22(11-15(14)24-17)10-13-6-4-3-5-7-13/h3-7,12H,8-11H2,1-2H3,(H,20,21)	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179325 (7-benzyl-2-(N-benzyl-N-methyl-amino)-5,6,7,8-tetra...) Show SMILES CN(Cc1ccccc1)c1nc2sc3CN(Cc4ccccc4)CCc3c2c(=O)o1 Show InChI InChI=1S/C24H23N3O2S/c1-26(14-17-8-4-2-5-9-17)24-25-22-21(23(28)29-24)19-12-13-27(16-20(19)30-22)15-18-10-6-3-7-11-18/h2-11H,12-16H2,1H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179314 (5,6,7,8-tetrahydro-2-(dimethylamino)-7-(2-methyl-p...) Show SMILES CC(C)CN1CCc2c(C1)sc1nc(oc(=O)c21)N(C)C Show InChI InChI=1S/C15H21N3O2S/c1-9(2)7-18-6-5-10-11(8-18)21-13-12(10)14(19)20-15(16-13)17(3)4/h9H,5-8H2,1-4H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair
Bile salt-activated lipase (Bos taurus)	BDBM50179312 (7-benzyl-5,6,7,8-tetrahydro-2-(dimethylamino)-4H-p...) Show SMILES CN(C)c1nc2sc3CN(Cc4ccccc4)CCc3c2c(=O)o1 Show InChI InChI=1S/C18H19N3O2S/c1-20(2)18-19-16-15(17(22)23-18)13-8-9-21(11-14(13)24-16)10-12-6-4-3-5-7-12/h3-7H,8-11H2,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inhibitory activity against bovine pancreatic CEase in presence of pNPB chromogenic substrate by spectrophotometry				J Med Chem 48: 8270-88 (2005) Article DOI: 10.1021/jm0508639 BindingDB Entry DOI: 10.7270/Q2GQ6XB4
					More data for this Ligand-Target Pair

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