Compile Data Set for Download or QSAR

Found 20 hits Enz. Inhib. hit(s) with all data for assayid = 2 entry = 50044102   

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
Cholinesterase (Equus caballus (Horse))	BDBM8961 (1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...) Show SMILES Nc1c2CCCCc2nc2ccccc12 Show InChI InChI=1S/C13H14N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1,3,5,7H,2,4,6,8H2,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	3.30	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair				3D Structure (crystal)
Cholinesterase (Equus caballus (Horse))	BDBM50002848 (CHEMBL3233940) Show SMILES COc1cc(Cn2c3ccccc3c(O)c(C(=O)NCC3CCN(Cc4ccccc4)CC3)c2=O)cc(OC)c1O Show InChI InChI=1S/C32H35N3O6/c1-40-26-16-23(17-27(41-2)30(26)37)20-35-25-11-7-6-10-24(25)29(36)28(32(35)39)31(38)33-18-21-12-14-34(15-13-21)19-22-8-4-3-5-9-22/h3-11,16-17,21,36-37H,12-15,18-20H2,1-2H3,(H,33,38)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	330	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002841 (CHEMBL3233933) Show SMILES Cn1c2ccccc2c(N)c(C(=O)NCC2CCN(Cc3ccccc3)CC2)c1=O Show InChI InChI=1S/C24H28N4O2/c1-27-20-10-6-5-9-19(20)22(25)21(24(27)30)23(29)26-15-17-11-13-28(14-12-17)16-18-7-3-2-4-8-18/h2-10,17H,11-16,25H2,1H3,(H,26,29)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.14E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM8960 ((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...) Show SMILES COc1cc2CC(CC3CCN(Cc4ccccc4)CC3)C(=O)c2cc1OC Show InChI InChI=1S/C24H29NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-8-10-25(11-9-17)16-18-6-4-3-5-7-18/h3-7,14-15,17,20H,8-13,16H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.82E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002853 (CHEMBL3233927) Show SMILES Cn1c2ccccc2c(O)c(C(=O)NCC2CCN(Cc3ccccc3)CC2)c1=O Show InChI InChI=1S/C24H27N3O3/c1-26-20-10-6-5-9-19(20)22(28)21(24(26)30)23(29)25-15-17-11-13-27(14-12-17)16-18-7-3-2-4-8-18/h2-10,17,28H,11-16H2,1H3,(H,25,29)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.26E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002851 (CHEMBL3233664) Show SMILES Oc1c(C(=O)NCC2CCN(Cc3ccccc3)CC2)c(=O)[nH]c2ccccc12 Show InChI InChI=1S/C23H25N3O3/c27-21-18-8-4-5-9-19(18)25-23(29)20(21)22(28)24-14-16-10-12-26(13-11-16)15-17-6-2-1-3-7-17/h1-9,16H,10-15H2,(H,24,28)(H2,25,27,29)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.02E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002839 (CHEMBL3233931) Show SMILES Cc1c(C(=O)NCC2CCN(Cc3ccccc3)CC2)c(=O)[nH]c2ccccc12 Show InChI InChI=1S/C24H27N3O2/c1-17-20-9-5-6-10-21(20)26-24(29)22(17)23(28)25-15-18-11-13-27(14-12-18)16-19-7-3-2-4-8-19/h2-10,18H,11-16H2,1H3,(H,25,28)(H,26,29)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002840 (CHEMBL3233932) Show SMILES O=C(NC1CCN(Cc2ccccc2)CC1)c1c(-c2ccccc2)c2ccccc2[nH]c1=O Show InChI InChI=1S/C28H27N3O2/c32-27(29-22-15-17-31(18-16-22)19-20-9-3-1-4-10-20)26-25(21-11-5-2-6-12-21)23-13-7-8-14-24(23)30-28(26)33/h1-14,22H,15-19H2,(H,29,32)(H,30,33)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002852 (CHEMBL3233926) Show SMILES Cn1c2ccccc2c(O)c(C(=O)NC2CCN(Cc3ccccc3)CC2)c1=O Show InChI InChI=1S/C23H25N3O3/c1-25-19-10-6-5-9-18(19)21(27)20(23(25)29)22(28)24-17-11-13-26(14-12-17)15-16-7-3-2-4-8-16/h2-10,17,27H,11-15H2,1H3,(H,24,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002843 (CHEMBL3233935) Show SMILES Oc1cc2[nH]c(=O)c(C(=O)NCC3CCN(Cc4ccccc4)CC3)c(O)c2cc1O Show InChI InChI=1S/C23H25N3O5/c27-18-10-16-17(11-19(18)28)25-23(31)20(21(16)29)22(30)24-12-14-6-8-26(9-7-14)13-15-4-2-1-3-5-15/h1-5,10-11,14,27-28H,6-9,12-13H2,(H,24,30)(H2,25,29,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002844 (CHEMBL3233936) Show SMILES Cl.COc1cc2c(O)c(C(=O)NCC3CCN(Cc4ccccc4)CC3)c(=O)n(C)c2cc1OC Show InChI InChI=1S/C26H31N3O5.ClH/c1-28-20-14-22(34-3)21(33-2)13-19(20)24(30)23(26(28)32)25(31)27-15-17-9-11-29(12-10-17)16-18-7-5-4-6-8-18;/h4-8,13-14,17,30H,9-12,15-16H2,1-3H3,(H,27,31);1H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002845 (CHEMBL3233937) Show SMILES Cn1c2cc(O)c(O)cc2c(O)c(C(=O)NCC2CCN(Cc3ccccc3)CC2)c1=O Show InChI InChI=1S/C24H27N3O5/c1-26-18-12-20(29)19(28)11-17(18)22(30)21(24(26)32)23(31)25-13-15-7-9-27(10-8-15)14-16-5-3-2-4-6-16/h2-6,11-12,15,28-30H,7-10,13-14H2,1H3,(H,25,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002837 (CHEMBL3233930) Show SMILES Cc1c(C(=O)NC2CCN(Cc3ccccc3)CC2)c(=O)[nH]c2ccccc12 Show InChI InChI=1S/C23H25N3O2/c1-16-19-9-5-6-10-20(19)25-23(28)21(16)22(27)24-18-11-13-26(14-12-18)15-17-7-3-2-4-8-17/h2-10,18H,11-15H2,1H3,(H,24,27)(H,25,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002854 (CHEMBL3233928) Show SMILES Oc1c(C(=O)NC2CCN(Cc3ccccc3)CC2)c(=O)n(Cc2ccccc2)c2ccccc12 Show InChI InChI=1S/C29H29N3O3/c33-27-24-13-7-8-14-25(24)32(20-22-11-5-2-6-12-22)29(35)26(27)28(34)30-23-15-17-31(18-16-23)19-21-9-3-1-4-10-21/h1-14,23,33H,15-20H2,(H,30,34)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002855 (CHEMBL3233929) Show SMILES Oc1c(C(=O)NCC2CCN(Cc3ccccc3)CC2)c(=O)n(Cc2ccccc2)c2ccccc12 Show InChI InChI=1S/C30H31N3O3/c34-28-25-13-7-8-14-26(25)33(21-24-11-5-2-6-12-24)30(36)27(28)29(35)31-19-22-15-17-32(18-16-22)20-23-9-3-1-4-10-23/h1-14,22,34H,15-21H2,(H,31,35)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002850 (CHEMBL3233663) Show SMILES Oc1c(C(=O)NC2CCN(Cc3ccccc3)CC2)c(=O)[nH]c2ccccc12 Show InChI InChI=1S/C22H23N3O3/c26-20-17-8-4-5-9-18(17)24-22(28)19(20)21(27)23-16-10-12-25(13-11-16)14-15-6-2-1-3-7-15/h1-9,16H,10-14H2,(H,23,27)(H2,24,26,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002847 (CHEMBL3233939) Show SMILES Cl.Oc1cc2c(O)c(C(=O)NCC3CCN(Cc4ccccc4)CC3)c(=O)n(Cc3ccccc3)c2cc1O Show InChI InChI=1S/C30H31N3O5.ClH/c34-25-15-23-24(16-26(25)35)33(19-22-9-5-2-6-10-22)30(38)27(28(23)36)29(37)31-17-20-11-13-32(14-12-20)18-21-7-3-1-4-8-21;/h1-10,15-16,20,34-36H,11-14,17-19H2,(H,31,37);1H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002849 (CHEMBL3233941) Show SMILES Oc1cc(Cn2c3ccccc3c(O)c(C(=O)NCC3CCN(Cc4ccccc4)CC3)c2=O)cc(O)c1O Show InChI InChI=1S/C30H31N3O6/c34-24-14-21(15-25(35)28(24)37)18-33-23-9-5-4-8-22(23)27(36)26(30(33)39)29(38)31-16-19-10-12-32(13-11-19)17-20-6-2-1-3-7-20/h1-9,14-15,19,34-37H,10-13,16-18H2,(H,31,38)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002842 (CHEMBL3233934) Show SMILES COc1cc2[nH]c(=O)c(C(=O)NCC3CCN(Cc4ccccc4)CC3)c(O)c2cc1OC Show InChI InChI=1S/C25H29N3O5/c1-32-20-12-18-19(13-21(20)33-2)27-25(31)22(23(18)29)24(30)26-14-16-8-10-28(11-9-16)15-17-6-4-3-5-7-17/h3-7,12-13,16H,8-11,14-15H2,1-2H3,(H,26,30)(H2,27,29,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>6.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50002846 (CHEMBL3233938) Show SMILES COc1cc2c(O)c(C(=O)NCC3CCN(Cc4ccccc4)CC3)c(=O)n(Cc3ccccc3)c2cc1OC Show InChI InChI=1S/C32H35N3O5/c1-39-27-17-25-26(18-28(27)40-2)35(21-24-11-7-4-8-12-24)32(38)29(30(25)36)31(37)33-19-22-13-15-34(16-14-22)20-23-9-5-3-6-10-23/h3-12,17-18,22,36H,13-16,19-21H2,1-2H3,(H,33,37)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>6.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Franche Comt£ Curated by ChEMBL					Assay Description Inhibition of BuChE in equine serum using butyrylthiocholine iodide as substrate preincubated with enzyme for 10 mins prior to substrate challenge me...				Bioorg Med Chem 22: 2496-507 (2014) Article DOI: 10.1016/j.bmc.2014.02.046 BindingDB Entry DOI: 10.7270/Q28K7BMT
					More data for this Ligand-Target Pair