Compile Data Set for Download or QSAR

Found 149 hits with Last Name = 'brenner' and Initial = 'e'   

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
Protease (Human immunodeficiency virus 1 (HIV-1))	BDBM50480930 (CHEMBL584130 | KNI-814) Show SMILES Cc1cccc(C)c1CNC(=O)[C@H]1N(CSC1(C)C)C(=O)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)c1cccc(O)c1C |r| Show InChI InChI=1S/C33H39N3O5S/c1-20-11-9-12-21(2)25(20)18-34-31(40)29-33(4,5)42-19-36(29)32(41)28(38)26(17-23-13-7-6-8-14-23)35-30(39)24-15-10-16-27(37)22(24)3/h6-16,26,28-29,37-38H,17-19H2,1-5H3,(H,34,40)(H,35,39)/t26-,28-,29+/m0/s1	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.00240	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant protease after 15 mins by fluorescence assay				J Med Chem 52: 7604-17 (2009) Article DOI: 10.1021/jm9005115 BindingDB Entry DOI: 10.7270/Q2FR00F2
					More data for this Ligand-Target Pair
Protease (Human immunodeficiency virus 1 (HIV-1))	BDBM580 ((4R)-3-[(2S,3S)-2-hydroxy-3-[(3-hydroxy-2-methylph...) Show SMILES Cc1ccccc1CNC(=O)[C@H]1N(CSC1(C)C)C(=O)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)c1cccc(O)c1C |r| Show InChI InChI=1S/C32H37N3O5S/c1-20-11-8-9-14-23(20)18-33-30(39)28-32(3,4)41-19-35(28)31(40)27(37)25(17-22-12-6-5-7-13-22)34-29(38)24-15-10-16-26(36)21(24)2/h5-16,25,27-28,36-37H,17-19H2,1-4H3,(H,33,39)(H,34,38)/t25-,27-,28+/m0/s1	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	MCE MMDB PC cid PC sid PDB UniChem Similars	PDB Article PubMed	0.0310	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant protease after 15 mins by fluorescence assay				J Med Chem 52: 7604-17 (2009) Article DOI: 10.1021/jm9005115 BindingDB Entry DOI: 10.7270/Q2FR00F2
					More data for this Ligand-Target Pair				3D Structure (crystal)
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50330326 ((4S,5R,6R)-5-Acetylamino-4-guanidino-6-((1R,3R)-1,...) Show SMILES [#6]-[#6](=O)-[#7]-[#6@@H]-1-[#6@H](-[#6]=[#6](-[#8]-[#6@H]-1-[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8])-[#6](-[#8])=O)\[#7]=[#6](\[#7])-[#7] |r,c:6| Show InChI InChI=1S/C12H20N4O7/c1-4(18)15-8-5(16-12(13)14)2-7(11(21)22)23-10(8)9(20)6(19)3-17/h2,5-6,8-10,17,19-20H,3H2,1H3,(H,15,18)(H,21,22)(H4,13,14,16)/t5-,6+,8+,9+,10+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	0.100	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair				3D Structure (crystal)
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50371257 (A-315675 | CHEMBL473062) Show SMILES CCC[C@](C)(OC)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O |r| Show InChI InChI=1S/C17H30N2O4/c1-6-8-12-10-13(16(21)22)19-14(12)15(18-11(3)20)17(4,23-5)9-7-2/h6,8,12-15,19H,7,9-10H2,1-5H3,(H,18,20)(H,21,22)/b8-6-/t12-,13-,14-,15-,17+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	0.140	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Protease (Human immunodeficiency virus 1 (HIV-1))	BDBM50480931 (CHEMBL575512 | KNI-1614) Show SMILES CC(=C)CNC(=O)[C@H]1N(CSC1(C)C)C(=O)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)c1cccc(O)c1C |r| Show InChI InChI=1S/C28H35N3O5S/c1-17(2)15-29-26(35)24-28(4,5)37-16-31(24)27(36)23(33)21(14-19-10-7-6-8-11-19)30-25(34)20-12-9-13-22(32)18(20)3/h6-13,21,23-24,32-33H,1,14-16H2,2-5H3,(H,29,35)(H,30,34)/t21-,23-,24+/m0/s1	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.190	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant protease after 15 mins by fluorescence assay				J Med Chem 52: 7604-17 (2009) Article DOI: 10.1021/jm9005115 BindingDB Entry DOI: 10.7270/Q2FR00F2
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233737 ((2R,4S,5R)-5-((R)-acetamido((S,Z)-2,3,4,7-tetrahyd...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@@H]1CCC=CCO1)C(O)=O |c:17| Show InChI InChI=1S/C17H26N2O4/c1-3-7-12-10-13(17(21)22)19-15(12)16(18-11(2)20)14-8-5-4-6-9-23-14/h3-4,6-7,12-16,19H,5,8-10H2,1-2H3,(H,18,20)(H,21,22)/b7-3-/t12-,13-,14+,15-,16+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.300	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233728 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-methoxybut-3-e...) Show SMILES CO[C@@H](C=C)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C15H24N2O4/c1-5-7-10-8-11(15(19)20)17-13(10)14(16-9(3)18)12(6-2)21-4/h5-7,10-14,17H,2,8H2,1,3-4H3,(H,16,18)(H,19,20)/b7-5-/t10-,11-,12+,13-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.600	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233741 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-methoxypent-4-...) Show SMILES CO[C@@H](CC=C)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C16H26N2O4/c1-5-7-11-9-12(16(20)21)18-14(11)15(17-10(3)19)13(22-4)8-6-2/h5-7,11-15,18H,2,8-9H2,1,3-4H3,(H,17,19)(H,20,21)/b7-5-/t11-,12-,13+,14-,15+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.670	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Protease (Human immunodeficiency virus 1 (HIV-1))	BDBM50480929 (CHEMBL573975 | KNI-1689) Show SMILES CC(=C)CNC(=O)[C@H]1N(CSC1(C)C)C(=O)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)COc1c(C)cc(N)cc1C |r| Show InChI InChI=1S/C30H40N4O5S/c1-18(2)15-32-28(37)27-30(5,6)40-17-34(27)29(38)25(36)23(14-21-10-8-7-9-11-21)33-24(35)16-39-26-19(3)12-22(31)13-20(26)4/h7-13,23,25,27,36H,1,14-17,31H2,2-6H3,(H,32,37)(H,33,35)/t23-,25-,27+/m0/s1	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid PDB UniChem	PDB Article PubMed	0.830	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Kyoto Pharmaceutical University Curated by ChEMBL					Assay Description Inhibition of HIV1 recombinant protease after 15 mins by fluorescence assay				J Med Chem 52: 7604-17 (2009) Article DOI: 10.1021/jm9005115 BindingDB Entry DOI: 10.7270/Q2FR00F2
					More data for this Ligand-Target Pair				3D Structure (crystal)
Transporter (Rattus norvegicus)	BDBM50198230 ((S)-2-((S)-(2-iodophenoxy)(phenyl)methyl)morpholin...) Show SMILES Ic1ccccc1O[C@H]([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C17H18INO2/c18-14-8-4-5-9-15(14)21-17(13-6-2-1-3-7-13)16-12-19-10-11-20-16/h1-9,16-17,19H,10-12H2/t16-,17-/m0/s1	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.840	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]nisoxetine from NET in rat brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM4994 ((3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)c...) Show SMILES CCC(CC)O[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(O)=O |r,c:7| Show InChI InChI=1S/C14H24N2O4/c1-4-10(5-2)20-12-7-9(14(18)19)6-11(15)13(12)16-8(3)17/h7,10-13H,4-6,15H2,1-3H3,(H,16,17)(H,18,19)/t11-,12+,13+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	1.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair				3D Structure (crystal)
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233723 ((2R,4S,5R)-5-((1R,2R)-1-acetamido-2-hydroxy-2-meth...) Show SMILES CCC[C@@](C)(O)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C16H28N2O4/c1-5-7-11-9-12(15(20)21)18-13(11)14(17-10(3)19)16(4,22)8-6-2/h5,7,11-14,18,22H,6,8-9H2,1-4H3,(H,17,19)(H,20,21)/b7-5-/t11-,12-,13-,14-,16-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233724 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-hydroxypentyl)...) Show SMILES CCC[C@H](O)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C15H26N2O4/c1-4-6-10-8-11(15(20)21)17-13(10)14(16-9(3)18)12(19)7-5-2/h4,6,10-14,17,19H,5,7-8H2,1-3H3,(H,16,18)(H,20,21)/b6-4-/t10-,11-,12+,13-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233732 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-hydroxypent-4-...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@@H](O)CC=C)C(O)=O Show InChI InChI=1S/C15H24N2O4/c1-4-6-10-8-11(15(20)21)17-13(10)14(16-9(3)18)12(19)7-5-2/h4-6,10-14,17,19H,2,7-8H2,1,3H3,(H,16,18)(H,20,21)/b6-4-/t10-,11-,12+,13-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233742 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-hydroxybut-3-e...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@@H](O)C=C)C(O)=O Show InChI InChI=1S/C14H22N2O4/c1-4-6-9-7-10(14(19)20)16-12(9)13(11(18)5-2)15-8(3)17/h4-6,9-13,16,18H,2,7H2,1,3H3,(H,15,17)(H,19,20)/b6-4-/t9-,10-,11+,12-,13+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Transporter (Rattus norvegicus)	BDBM50198226 (2-((2-iodophenoxy)(phenyl)methyl)morpholine | CHEM...) Show SMILES Ic1ccccc1OC(C1CNCCO1)c1ccccc1 |w:9.10,8.8| Show InChI InChI=1S/C17H18INO2/c18-14-8-4-5-9-15(14)21-17(13-6-2-1-3-7-13)16-12-19-10-11-20-16/h1-9,16-17,19H,10-12H2	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.47	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]nisoxetine from NET in rat brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233744 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-hydroxybutyl)-...) Show SMILES CC[C@H](O)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C14H24N2O4/c1-4-6-9-7-10(14(19)20)16-12(9)13(11(18)5-2)15-8(3)17/h4,6,9-13,16,18H,5,7H2,1-3H3,(H,15,17)(H,19,20)/b6-4-/t9-,10-,11+,12-,13+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233726 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-ethoxybut-3-en...) Show SMILES CCO[C@@H](C=C)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C16H26N2O4/c1-5-8-11-9-12(16(20)21)18-14(11)15(17-10(4)19)13(6-2)22-7-3/h5-6,8,11-15,18H,2,7,9H2,1,3-4H3,(H,17,19)(H,20,21)/b8-5-/t11-,12-,13+,14-,15+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233725 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-hydroxypropyl)...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@H](C)O)C(O)=O Show InChI InChI=1S/C13H22N2O4/c1-4-5-9-6-10(13(18)19)15-12(9)11(7(2)16)14-8(3)17/h4-5,7,9-12,15-16H,6H2,1-3H3,(H,14,17)(H,18,19)/b5-4-/t7-,9+,10+,11-,12+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233727 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-(allyloxy)but-...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@@H](OCC=C)C=C)C(O)=O Show InChI InChI=1S/C17H26N2O4/c1-5-8-12-10-13(17(21)22)19-15(12)16(18-11(4)20)14(7-3)23-9-6-2/h5-8,12-16,19H,2-3,9-10H2,1,4H3,(H,18,20)(H,21,22)/b8-5-/t12-,13-,14+,15-,16+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233722 ((2R,4S,5R)-5-((R)-acetamido((R)-3,6-dihydro-2H-pyr...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@H]1CC=CCO1)C(O)=O |c:16| Show InChI InChI=1S/C16H24N2O4/c1-3-6-11-9-12(16(20)21)18-14(11)15(17-10(2)19)13-7-4-5-8-22-13/h3-6,11-15,18H,7-9H2,1-2H3,(H,17,19)(H,20,21)/b6-3-/t11-,12-,13-,14-,15+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	10.3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233733 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-ethoxypent-4-e...) Show SMILES CCO[C@@H](CC=C)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C17H28N2O4/c1-5-8-12-10-13(17(21)22)19-15(12)16(18-11(4)20)14(9-6-2)23-7-3/h5-6,8,12-16,19H,2,7,9-10H2,1,3-4H3,(H,18,20)(H,21,22)/b8-5-/t12-,13-,14+,15-,16+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	10.6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233740 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-hydroxyhexyl)-...) Show SMILES CCCC[C@H](O)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C16H28N2O4/c1-4-6-8-13(20)15(17-10(3)19)14-11(7-5-2)9-12(18-14)16(21)22/h5,7,11-15,18,20H,4,6,8-9H2,1-3H3,(H,17,19)(H,21,22)/b7-5-/t11-,12-,13+,14-,15+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Sodium-dependent dopamine transporter (Rattus norvegicus (rat))	BDBM50198231 (2-((2-nitrobenzyloxy)(3-iodophenyl)methyl)morpholi...) Show SMILES [O-][N+](=O)c1ccccc1COC(C1CNCCO1)c1cccc(I)c1 |w:12.13,11.11| Show InChI InChI=1S/C18H19IN2O4/c19-15-6-3-5-13(10-15)18(17-11-20-8-9-24-17)25-12-14-4-1-2-7-16(14)21(22)23/h1-7,10,17-18,20H,8-9,11-12H2	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	14.2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]GBR from DAT in rat brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Transporter (Rattus norvegicus)	BDBM50198233 (2-((3-iodophenyl)(2-methoxyphenoxy)methyl)morpholi...) Show SMILES COc1ccccc1OC(C1CNCCO1)c1cccc(I)c1 |w:10.11,9.9| Show InChI InChI=1S/C18H20INO3/c1-21-15-7-2-3-8-16(15)23-18(17-12-20-9-10-22-17)13-5-4-6-14(19)11-13/h2-8,11,17-18,20H,9-10,12H2,1H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	15.4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]nisoxetine from NET in rat brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233743 ((2R,4S,5R)-5-((1R,2S)-1-acetamido-2-(allyloxy)pent...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@H](CC=C)OCC=C)C(O)=O Show InChI InChI=1S/C18H28N2O4/c1-5-8-13-11-14(18(22)23)20-16(13)17(19-12(4)21)15(9-6-2)24-10-7-3/h5-8,13-17,20H,2-3,9-11H2,1,4H3,(H,19,21)(H,22,23)/b8-5-/t13-,14-,15+,16-,17+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	17.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus (A/Tokyo/3/67(H2N2)))	BDBM5202 ((+/-)-(2R,4S,5R,1 S)-5-(1 -Acetylamino-3 -methyl-b...) Show SMILES [H][C@]1(N[C@H](C[C@H]1\C=C/C)C(O)=O)[C@H](CC(C)C)NC(C)=O |r| Show InChI InChI=1S/C15H26N2O3/c1-5-6-11-8-13(15(19)20)17-14(11)12(7-9(2)3)16-10(4)18/h5-6,9,11-14,17H,7-8H2,1-4H3,(H,16,18)(H,19,20)/b6-5-/t11-,12+,13-,14-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories					Assay Description A fluorogenic assay was used to measure influenza virus neuraminidase activity. The substrate, 4-methylumbelliferyl-N-acetylneuraminic acid, is cleav...				J Med Chem 48: 3980-90 (2005) Article DOI: 10.1021/jm049276y BindingDB Entry DOI: 10.7270/Q2KP80B9
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233731 ((2R,4S,5R)-5-((1R,2R)-1-acetamido-2-hydroxybut-3-e...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@H](O)C=C)C(O)=O Show InChI InChI=1S/C14H22N2O4/c1-4-6-9-7-10(14(19)20)16-12(9)13(11(18)5-2)15-8(3)17/h4-6,9-13,16,18H,2,7H2,1,3H3,(H,15,17)(H,19,20)/b6-4-/t9-,10-,11-,12-,13+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	21	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233721 ((2R,4S,5R)-5-((R)-acetamido((S)-3,6-dihydro-2H-pyr...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@@H]1CC=CCO1)C(O)=O |c:16| Show InChI InChI=1S/C16H24N2O4/c1-3-6-11-9-12(16(20)21)18-14(11)15(17-10(2)19)13-7-4-5-8-22-13/h3-6,11-15,18H,7-9H2,1-2H3,(H,17,19)(H,20,21)/b6-3-/t11-,12-,13+,14-,15+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	24.2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Transporter (Rattus norvegicus)	BDBM50198232 (2-((3-iodophenyl)(o-tolyloxy)methyl)morpholine | C...) Show SMILES Cc1ccccc1OC(C1CNCCO1)c1cccc(I)c1 |w:9.10,8.8| Show InChI InChI=1S/C18H20INO2/c1-13-5-2-3-8-16(13)22-18(17-12-20-9-10-21-17)14-6-4-7-15(19)11-14/h2-8,11,17-18,20H,9-10,12H2,1H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	27.6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]nisoxetine from NET in rat brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233730 ((2R,4S,5R)-5-((1R,2R)-1-acetamido-2-hydroxypentyl)...) Show SMILES CCC[C@@H](O)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C15H26N2O4/c1-4-6-10-8-11(15(20)21)17-13(10)14(16-9(3)18)12(19)7-5-2/h4,6,10-14,17,19H,5,7-8H2,1-3H3,(H,16,18)(H,20,21)/b6-4-/t10-,11-,12-,13-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	28	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Transporter (Rattus norvegicus)	BDBM50198227 (2-((2-ethoxyphenoxy)(3-iodophenyl)methyl)morpholin...) Show SMILES CCOc1ccccc1OC(C1CNCCO1)c1cccc(I)c1 |w:11.12,10.10| Show InChI InChI=1S/C19H22INO3/c1-2-22-16-8-3-4-9-17(16)24-19(18-13-21-10-11-23-18)14-6-5-7-15(20)12-14/h3-9,12,18-19,21H,2,10-11,13H2,1H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	28.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]nisoxetine from NET in rat brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233738 ((2R,4S,5R)-5-((1R,2R)-1-acetamido-2-hydroxybutyl)-...) Show SMILES CC[C@@H](O)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C14H24N2O4/c1-4-6-9-7-10(14(19)20)16-12(9)13(11(18)5-2)15-8(3)17/h4,6,9-13,16,18H,5,7H2,1-3H3,(H,15,17)(H,19,20)/b6-4-/t9-,10-,11-,12-,13+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	29	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Memphis/3/93))	BDBM5202 ((+/-)-(2R,4S,5R,1 S)-5-(1 -Acetylamino-3 -methyl-b...) Show SMILES [H][C@]1(N[C@H](C[C@H]1\C=C/C)C(O)=O)[C@H](CC(C)C)NC(C)=O |r| Show InChI InChI=1S/C15H26N2O3/c1-5-6-11-8-13(15(19)20)17-14(11)12(7-9(2)3)16-10(4)18/h5-6,9,11-14,17H,7-8H2,1-4H3,(H,16,18)(H,19,20)/b6-5-/t11-,12+,13-,14-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories					Assay Description A fluorogenic assay was used to measure influenza virus neuraminidase activity. The substrate, 4-methylumbelliferyl-N-acetylneuraminic acid, is cleav...				J Med Chem 48: 3980-90 (2005) Article DOI: 10.1021/jm049276y BindingDB Entry DOI: 10.7270/Q2KP80B9
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM5202 ((+/-)-(2R,4S,5R,1 S)-5-(1 -Acetylamino-3 -methyl-b...) Show SMILES [H][C@]1(N[C@H](C[C@H]1\C=C/C)C(O)=O)[C@H](CC(C)C)NC(C)=O |r| Show InChI InChI=1S/C15H26N2O3/c1-5-6-11-8-13(15(19)20)17-14(11)12(7-9(2)3)16-10(4)18/h5-6,9,11-14,17H,7-8H2,1-4H3,(H,16,18)(H,19,20)/b6-5-/t11-,12+,13-,14-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233735 ((2R,4S,5R)-5-((1R,2R)-1-acetamido-2-methoxypent-4-...) Show SMILES CO[C@H](CC=C)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C16H26N2O4/c1-5-7-11-9-12(16(20)21)18-14(11)15(17-10(3)19)13(22-4)8-6-2/h5-7,11-15,18H,2,8-9H2,1,3-4H3,(H,17,19)(H,20,21)/b7-5-/t11-,12-,13-,14-,15+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	38	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Rattus norvegicus (rat))	BDBM50198230 ((S)-2-((S)-(2-iodophenoxy)(phenyl)methyl)morpholin...) Show SMILES Ic1ccccc1O[C@H]([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C17H18INO2/c18-14-8-4-5-9-15(14)21-17(13-6-2-1-3-7-13)16-12-19-10-11-20-16/h1-9,16-17,19H,10-12H2/t16-,17-/m0/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	40.4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]paroxetine from SERT in brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus (A/Tokyo/3/67(H2N2)))	BDBM5200 ((+/-)-(2R,4R,5R,1 S)-5-(1 -Acetylamino-3 -methylbu...) Show SMILES [H][C@]1(N[C@H](C[C@H]1c1ccn[nH]1)C(O)=O)[C@H](CC(C)C)NC(C)=O |r| Show InChI InChI=1S/C15H24N4O3/c1-8(2)6-12(17-9(3)20)14-10(11-4-5-16-19-11)7-13(18-14)15(21)22/h4-5,8,10,12-14,18H,6-7H2,1-3H3,(H,16,19)(H,17,20)(H,21,22)/t10-,12-,13+,14+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	45	-41.5	n/a	n/a	n/a	n/a	n/a	7.5	22
Abbott Laboratories					Assay Description A fluorogenic assay was used to measure influenza virus neuraminidase activity. The substrate, 4-methylumbelliferyl-N-acetylneuraminic acid, is cleav...				J Med Chem 48: 3980-90 (2005) Article DOI: 10.1021/jm049276y BindingDB Entry DOI: 10.7270/Q2KP80B9
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233736 ((2R,4S,5R)-5-((1R,2R)-1-acetamido-2-ethoxypent-4-e...) Show SMILES CCO[C@H](CC=C)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C17H28N2O4/c1-5-8-12-10-13(17(21)22)19-15(12)16(18-11(4)20)14(9-6-2)23-7-3/h5-6,8,12-16,19H,2,7,9-10H2,1,3-4H3,(H,18,20)(H,21,22)/b8-5-/t12-,13-,14-,15-,16+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	46	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233729 ((2R,4S,5R)-5-((1R,2R)-1-acetamido-2-hydroxypent-4-...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@H](O)CC=C)C(O)=O Show InChI InChI=1S/C15H24N2O4/c1-4-6-10-8-11(15(20)21)17-13(10)14(16-9(3)18)12(19)7-5-2/h4-6,10-14,17,19H,2,7-8H2,1,3H3,(H,16,18)(H,20,21)/b6-4-/t10-,11-,12-,13-,14+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	49	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Memphis/3/93))	BDBM5200 ((+/-)-(2R,4R,5R,1 S)-5-(1 -Acetylamino-3 -methylbu...) Show SMILES [H][C@]1(N[C@H](C[C@H]1c1ccn[nH]1)C(O)=O)[C@H](CC(C)C)NC(C)=O |r| Show InChI InChI=1S/C15H24N4O3/c1-8(2)6-12(17-9(3)20)14-10(11-4-5-16-19-11)7-13(18-14)15(21)22/h4-5,8,10,12-14,18H,6-7H2,1-3H3,(H,16,19)(H,17,20)(H,21,22)/t10-,12-,13+,14+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	57	-40.9	n/a	n/a	n/a	n/a	n/a	7.5	22
Abbott Laboratories					Assay Description A fluorogenic assay was used to measure influenza virus neuraminidase activity. The substrate, 4-methylumbelliferyl-N-acetylneuraminic acid, is cleav...				J Med Chem 48: 3980-90 (2005) Article DOI: 10.1021/jm049276y BindingDB Entry DOI: 10.7270/Q2KP80B9
					More data for this Ligand-Target Pair
Transporter (Rattus norvegicus)	BDBM50198231 (2-((2-nitrobenzyloxy)(3-iodophenyl)methyl)morpholi...) Show SMILES [O-][N+](=O)c1ccccc1COC(C1CNCCO1)c1cccc(I)c1 |w:12.13,11.11| Show InChI InChI=1S/C18H19IN2O4/c19-15-6-3-5-13(10-15)18(17-11-20-8-9-24-17)25-12-14-4-1-2-7-16(14)21(22)23/h1-7,10,17-18,20H,8-9,11-12H2	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	70.4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]nisoxetine from NET in rat brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Transporter (Rattus norvegicus)	BDBM50198234 (2-((5-iodothiophen-2-yl)(o-tolyloxy)methyl)morphol...) Show SMILES Cc1ccccc1OC(C1CNCCO1)c1ccc(I)s1 |w:9.15,8.8| Show InChI InChI=1S/C16H18INO2S/c1-11-4-2-3-5-12(11)20-16(13-10-18-8-9-19-13)14-6-7-15(17)21-14/h2-7,13,16,18H,8-10H2,1H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	71.9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]nisoxetine from NET in rat brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Transporter (Rattus norvegicus)	BDBM50198225 (2-((2-methoxybenzyloxy)(3-iodophenyl)methyl)morpho...) Show SMILES COc1ccccc1COC(C1CNCCO1)c1cccc(I)c1 |w:11.17,10.10| Show InChI InChI=1S/C19H22INO3/c1-22-17-8-3-2-5-15(17)13-24-19(18-12-21-9-10-23-18)14-6-4-7-16(20)11-14/h2-8,11,18-19,21H,9-10,12-13H2,1H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	73.8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]nisoxetine from NET in rat brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus (A/Tokyo/3/67(H2N2)))	BDBM5207 ((+/-)-(2R,4S,5R,1 S)-5-(1 -Acetylamino-3 -methyl-b...) Show SMILES [H][C@]1(N[C@H](C[C@H]1\C=C/Cl)C(O)=O)[C@H](CC(C)C)NC(C)=O |r| Show InChI InChI=1S/C14H23ClN2O3/c1-8(2)6-11(16-9(3)18)13-10(4-5-15)7-12(17-13)14(19)20/h4-5,8,10-13,17H,6-7H2,1-3H3,(H,16,18)(H,19,20)/b5-4-/t10-,11+,12-,13-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	79	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories					Assay Description A fluorogenic assay was used to measure influenza virus neuraminidase activity. The substrate, 4-methylumbelliferyl-N-acetylneuraminic acid, is cleav...				J Med Chem 48: 3980-90 (2005) Article DOI: 10.1021/jm049276y BindingDB Entry DOI: 10.7270/Q2KP80B9
					More data for this Ligand-Target Pair
Transporter (Rattus norvegicus)	BDBM50198228 (2-((5-iodothiophen-2-yl)(2-methoxyphenoxy)methyl)m...) Show SMILES COc1ccccc1OC(C1CNCCO1)c1ccc(I)s1 |w:10.16,9.9| Show InChI InChI=1S/C16H18INO3S/c1-19-11-4-2-3-5-12(11)21-16(13-10-18-8-9-20-13)14-6-7-15(17)22-14/h2-7,13,16,18H,8-10H2,1H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	79.6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]nisoxetine from NET in rat brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233745 ((2R,4S,5R)-5-((1R,2R)-1-acetamido-2-hydroxypropyl)...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@@H](C)O)C(O)=O Show InChI InChI=1S/C13H22N2O4/c1-4-5-9-6-10(13(18)19)15-12(9)11(7(2)16)14-8(3)17/h4-5,7,9-12,15-16H,6H2,1-3H3,(H,14,17)(H,18,19)/b5-4-/t7-,9-,10-,11+,12-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	85	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233739 ((2R,4S,5R)-5-((1R,2R)-1-acetamido-2-hydroxyhexyl)-...) Show SMILES CCCC[C@@H](O)[C@H](NC(C)=O)[C@@H]1N[C@H](C[C@H]1\C=C/C)C(O)=O Show InChI InChI=1S/C16H28N2O4/c1-4-6-8-13(20)15(17-10(3)19)14-11(7-5-2)9-12(18-14)16(21)22/h5,7,11-15,18,20H,4,6,8-9H2,1-3H3,(H,17,19)(H,21,22)/b7-5-/t11-,12-,13-,14-,15+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	86	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair
Transporter (Rattus norvegicus)	BDBM50198229 (2-((3-iodophenyl)(2-(trifluoromethyl)phenoxy)methy...) Show SMILES FC(F)(F)c1ccccc1OC(C1CNCCO1)c1cccc(I)c1 |w:12.13,11.11| Show InChI InChI=1S/C18H17F3INO2/c19-18(20,21)14-6-1-2-7-15(14)25-17(16-11-23-8-9-24-16)12-4-3-5-13(22)10-12/h1-7,10,16-17,23H,8-9,11H2	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	101	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Degenerative Diseases Curated by ChEMBL					Assay Description Displacement of [3H]nisoxetine from NET in rat brain membranes				Bioorg Med Chem Lett 17: 533-7 (2007) Article DOI: 10.1016/j.bmcl.2006.10.018 BindingDB Entry DOI: 10.7270/Q2WS8SX8
					More data for this Ligand-Target Pair
Neuraminidase (Influenza B virus (B/Lee/40))	BDBM50233734 ((2R,4S,5R)-5-((1R,2R)-1-acetamido-2-(allyloxy)pent...) Show SMILES C\C=C/[C@@H]1C[C@@H](N[C@H]1[C@@H](NC(C)=O)[C@@H](CC=C)OCC=C)C(O)=O Show InChI InChI=1S/C18H28N2O4/c1-5-8-13-11-14(18(22)23)20-16(13)17(19-12(4)21)15(9-6-2)24-10-7-3/h5-8,13-17,20H,2-3,9-11H2,1,4H3,(H,19,21)(H,22,23)/b8-5-/t13-,14-,15-,16-,17+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	110	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of influenza B/Memphis/3/89 neuraminidase				Bioorg Med Chem Lett 18: 1692-5 (2008) Article DOI: 10.1016/j.bmcl.2008.01.048 BindingDB Entry DOI: 10.7270/Q2WW7JHN
					More data for this Ligand-Target Pair

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